Current and emerging drugs for the treatment of inflammatory bowel disease.

During the last decade a large number of biological agents against tumor necrosis factor-α (TNF-α), as well as many biochemical substances and molecules specifically for the medical treatment of patients with inflammatory bowel disease (IBD), have been developed. This enormous progress was a consequence of the significant advances in biotechnology along with the increased knowledge of the underlying pathophysiological mechanisms involved in the pathogenesis of IBD. However, conventional therapies remain the cornerstone of treatment for most patients. During recent years conventional and biologic IBD therapies have been optimized. Newer mesalazine formulations with a reduced pill size and only one dose per day demonstrate similar efficacy to older formulations. New corticosteroids retain the efficacy of older corticosteroids while exhibiting a higher safety profile. The role of antibiotics and probiotics has been further clarified. Significant progress in understanding thiopurine metabolism has improved the effective dose along with adjunctive therapies. Quite a large number of substances and therapies, including biologic agents other than TNF-α inhibitors, unfractionated or low-molecular-weight heparin, omega-3 polyunsaturated fatty acids, microbes and microbial products, leukocytapheresis, and other substances under investigation, could offer important benefits to our patients. In this paper we review the established and emerging therapeutic strategies in patients with Crohn's disease and ulcerative colitis.

Introduction

Inflammatory bowel disease (IBD) is a chronic, relapsing, inflammatory disorder of the gastrointestinal tract that includes two entities, namely Crohn’s disease (CD) and ulcerative colitis (UC). In the last decade, our understanding of the etiology and pathogenesis of IBD has improved considerably.

Treatment of the disease includes conservative measures as well as surgical approaches in those who are non-responders to medical treatment. The primary therapeutic goals are related to improvement of patient quality of life by inducing and maintaining remission, predicting, preventing and treating complications, restoring nutritional deficits, providing appropriate psychosocial support, and modifying the course in those with aggressive disease.

Pharmaceutical treatment of IBD includes five major categories, namely anti-inflammatory drugs, immunosuppressants, biologic agents, antibiotics, and drugs for symptomatic relief. Several other pharmaceutical substances have been produced and studied in recent years, the implementation of which was the result of an increased knowledge of the underlying pathophysiological mechanisms.

There is now a general consensus that IBD is the result of the combined effects of 4 factors: environmental influences, genetic variations, intestinal microbiota alterations, and disturbances in the innate and adaptive immune responses. A combination of all these factors is probably necessary for the disease to be clinically expressed. However, it seems that each patient has a different combination of factors leading to the disease, explaining why each patient displays their own clinical picture and response to therapy.1

The intestine is the largest lymphoid organ in the body because of the huge antigen load to which it is exposed on a daily basis. The mucosa-associated lymphoid tissue of the bowel is regulated by unique mechanisms, as reflected in oral tolerance, physiologic inflammation, and intraepithelial lymphocytes that respond to alternative pathways of activation. Moreover, the existence of novel antigen-presenting cells is responsible for distinct immune responses.

Altered immune responses are considered to be quite important elements related to the pathogenesis of IBD. The innate immune system plays a significant role in the defense mechanisms by recognizing bacterial products and cellular signaling. The abnormal signaling pathways can lead to dysregulation of the inflammatory response. Impairment of this system results in activation of the adaptive immune system leading to excessive proinflammatory cytokine production derived from CD4+ T cells over and above the response normally associated with tolerance and immunoregulation.2

Intestinal epithelial cell barrier function is also considered to be an important part of the immune defense of the host. Inappropriate access of antigens to the mucosal immune system through dysfunctional barrier function represents an important element in the IBD pathophysiology.

Genetic predisposition affects the regulation of innate and adaptive immunity. Therefore, immunogenetic pathways associated with innate and adaptive immunity, cytokines secreted by innate and adaptive immune cells, epithelial and leukocyte factors, and structures on the endothelium that regulate the recruitment of leukocytes define pathways that could be therapeutic targets.

There are some differences between CD and UC in the underlying immunological disturbances. In CD the antigen presenting cells and macrophages produce mainly interleukin-12 (IL-12) and IL-18 resulting in a Th1-type polarization and production of pro-inflammatory cytokines including tumor necrosis factor-α (TNF-α), interferon-γ (IFN-γ), and IL-2. Subsequently these cytokines stimulate the antigen presenting cells to secrete other cytokines including IL-1, IL-6, IL-8, IL-12, and IL-18, thus leading to a self-sustained cycle.3

Patients with UC exhibit an added contribution of Th2 responses characterized by increased secretion of IL-4, IL-5, and IL-13 and reduced amounts of IFN-γ. Th17 cells were identified as a new subset of T helper cells unrelated to Th1 or Th2 cells. Th17 cells differentiate under the influence of IL-1β, IL-6, IL-21 and IL-23.4 Recently it was shown that transforming growth factor-β (TGF-β) regulates also the differentiation of Th17 cells, with the presence of cytokines favoring Th17 cell differentiation.5

Additionally, other molecules involved in leukocyte trafficking (adhesion molecules), chemokines, and tissue repair molecules are also crucial in the pathogenesis of the disease. In IBD continuous production of pro-inflammatory cytokines results in an inappropriately increased adhesion molecule expression, as well as in an aberrant expression of molecules not normally expressed by specific lymphocyte subpopulations.6

In recent years the knowledge of all these complex pathophysiological processes has resulted in the implementation of a number of different pharmaceutical agents in the treatment of IBD. These drugs were designed to minimize the inflammatory process through inhibition of different targets.

In this review we will try to describe the established and emerging therapeutic strategies in patients with IBD.

Drugs currently in use in patients with IBD

Conventional therapies remain the cornerstone of treatment for the majority of patients with IBD, only a proportion of whom require biologic therapies. During recent years attention has been given to the optimization of conventional and biologic IBD therapies. Newer mesalazine formulations with a reduced pill size and only one dose per day demonstrate similar efficacy to older formulations. New corticosteroids (CSs) retain the efficacy of older CSs while exhibiting a higher safety profile. The role of antibiotics and probiotics has been further clarified. Finally, significant progress in understanding thiopurine metabolism has improved the effective dose along with adjunctive therapies.

Table 1 shows the drug categories currently used in the treatment of patients with IBD.

Table 1

Established drug categories used in the treatment of inflammatory bowel disease

Drug group	Drugs
Anti-inflammatory	Mesalazine Corticosteroids (prednisolone, methylprednisolone, butesonide)
Immunosuppressives	Azathioprine, 6-mercaptopurine, methotrexate, cyclosporin, tacrolimus
Antibiotics	Metronidazole, ornidazole, clarithromycin, rifaximin ciprofloxacin, anti-TB
Probiotics
Biologics	Infliximab, adalimumab, certolizumab pegol

Abbreviation: TB, tuberculosis.

Anti-inflammatory drugs

Mesalazine

Mesalazine, the active moiety of sulfasalazine, is available in specially formulated oral and rectal forms for the treatment of active UC of mild to moderate severity and for maintenance therapy during disease remission.

The new preparations of mesalazine offer convenience and high dosage, while retaining their safety. New dosage regimens are likely to become standard practice in the near future. The drug might also act as a chemopreventive agent of colorectal cancer in the context of IBD, probably via the agonism of the peroxisome proliferator-activated receptor-γ (PPAR-γ). In future, even more effective agents based on mesalazine are expected, based on more powerful agonism of PPAR-γ. Mesalazine, either in tablets coated with acrylic-based resin or microgranules coated with ethylcellulose can be delivered to the distal small intestine and colon.7

Mesalazine in ulcerative colitis

Orally administered mesalazine represents an effective drug in the treatment of patients with mild to moderate active distal UC and for maintaining remission. In cases of distal UC mesalazine can also be administered rectally as a suppository, enema, or foam.8

Oral mesalazine in a dose of 1.5 to 2.4 g daily has similar efficacy to sulfasalazine 2 to 3 g daily in patients with mild to moderate UC. Mesalazine enemas once a day are more effective than placebo and apparently similar to enemas of prednisone 25 mg or oral sulfasalazine 3 g. Mesalazine 4 g enemas are more effective than enemas containing hydrocortisone 100 mg.

Once-daily dosing of delayed-release mesalazine at doses of 1.6 to 2.4 g/day was shown to be as effective as twice-daily dosing for maintenance of clinical remission in patients with UC, thus increasing the compliance of the patients.9

Balsalazide disodium 1.1 g tablets administered as 3.3 g twice daily are effective, well-tolerated, and significantly better than placebo for improving signs and symptoms of mild-to-moderately active UC.10 Again, this new formulation is expected to significantly improve convenience and compliance of patients with active UC.

The ASCEND I study showed that delayed-release oral mesalazine is an effective and well-tolerated therapy in patients with mildly to moderately active UC, and a 4.8 g/day dose (Asacol® HD, 800-mg tablet; Procter and Gamble, Pharmaceuticals, Inc, Mason, OH) may improve treatment success in patients with moderate disease compared with mesalazine 2.4 g/day (Asacol, 400-mg tablet).11

The ASCEND III study was designed to determine the efficacy and safety of mesalazine 4.8 g/day (Asacol HD, 800-mg tablet) compared with 2.4 g/day (Asacol, 400-mg tablet) in moderately active UC. The results showed that 70% of patients who received 4.8 g/day achieved treatment success at week 6, compared with 66% of patients receiving 2.4 g/day.12

In a study aiming to determine the therapeutic equivalence and safety of once daily versus 3 times daily dosing of a total daily dose of 3 g mesalazine granules (Salofalk®, Dr Falk Pharma GmBH, Freiburg, Germany) in patients with active UC it was shown that once daily 3 g mesalazine granules are as effective and safe as a three times daily of 1 g schedule.13

Most patients with mild-to-moderate UC who fail to achieve remission with up to 8 weeks’ initial mesalazine therapy could achieve clinical and endoscopic remission following a further 8 weeks’ treatment with high-dose MMX technology (Multi Matrix System) mesalazine therapy (Mezavant® tablet 1.2 g; Shire, Dublin, Ireland).14

Two phase III studies have evaluated mesalazine with MMX technology in patients with active mild-to-moderate UC and shown it to be effective regardless of disease extent and severity, gender, and previous low-dose mesalazine therapy.15

Conclusion

Mesalazine is an effective drug in the treatment of mild-to-moderately active distal UC at a dose of 2.4 to 4.8 g/day. Once daily dosing should be the preferred application mode in active UC. The drug is generally well tolerated with few side-effects reported. However, patients must check their renal function at 6-month intervals. Mesalazine can also be tolerated by 85% of patients allergic to or intolerant of sulfasalazine. Side-effects of mesalazine enemas are confined to local irritation.16

Mesalazine in Crohn’s disease

A recent meta-analysis evaluated the efficacy of aminosalicylates compared with placebo, CSs, and other aminosalicylates in active CD.17

The results revealed that sulfasalazine was superior to placebo in inducing remission, with benefit confined mainly to patients with colitis, although it was less effective than CSs.

Low-dose mesalazine (1–2 g/day) did not differ from placebo and was less effective than CSs, while high-dose mesalazine (3–4.5 g/day) was not superior to placebo for induction of remission or response. Mesalazine could also be less effective than budesonide.17

Prevention of relapses in patients operated on for CD represent a rather difficult task. In a trial aiming to compare azathioprine (AZ) with mesalazine for the prevention of recurrence in patients with postoperative CD, AZ did not show better results than mesalazine.18

The available data do not support a role for mesalazine in the treatment of active CD.

Corticosteroids

CSs suppress inflammation by blocking the early manifestations of inflammation, including enhanced vascular permeability, vasodilation, and infiltration by neutrophils as well as the later consequences of inflammation, including fibroblast activation, vascular proliferation, and deposition of collagen. CSs also influence immunological responses such as T-responses to antigens, downregulate production of inflammatory cytokines, and interfere with nuclear factor-κB (NF-κB) production, thereby blunting inflammatory response.19

CSs can be administered orally, in the form of enemas, or systematically in conjunction with or without other drugs. The most widely used CSs are prednisolone, methylprednisolone, and budesonide.

Corticosteroids in ulcerative colitis

The dose and route of administration of CSs in active UC depends on the severity of the disease and ranges from 20 to 40 and 50 to 60 mg/day for moderate and severe flare-ups, respectively. Subsequently, the dose should be reduced by 10 or 5 mg/week depending on the clinical and endoscopic remission.20 In severe cases CSs should be given parenterally for at least 10 days. If there are no clinical or laboratory signs of improvement the patient must be treated with cyclosporin or biologic agents. CSs are not useful for maintenance treatment of UC.

Budesonide is an enteric-coated, locally acting CS, whose pH- and time-dependent coating enables its release into the ileum and ascending colon. There is no evidence to recommend the clinical use of oral budesonide for the induction of remission in active UC.21

Corticosteroids in Crohn’s disease

CSs are highly effective drugs for induction of remission in patients with active CD. The various formulations of CSs can induce fast remission, improving most of the symptoms in a few days, although they cannot achieve mucosal healing and they have a number of side-effects. In a Cochrane meta-analysis CSs were highly significantly more effective than placebo and mesalazine in inducing remission. It should be emphasized that although CSs cause more adverse events than either placebo or low-dose mesalazine, these adverse events did not lead to increased study withdrawal.22 Some patients could become steroid-dependend or steroid resistant. CSs are not useful for maintenance treatment of CD.

Budesonide treatment for up to 1 year is well tolerated, with an adverse-event profile similar to that of placebo.22 The 1-year relapse rates are low and not significantly different between patients treated with budesonide 6 mg versus 9 mg/day. Time to relapse and the number of adverse events are similar in both groups.14 Budesonide may be a safe option for treatment of CD during pregnancy.23

CSs remain the cornerstone of initial therapy in both active CD and active UC. One-third of patients will fail to respond. Subsequent management of this proportion of patients involves decisions on whether to use cyclosporin or infliximab without compromising the health or safety of the patient, or to offer surgical treatment. Further studies are required in order to determine the optimal duration of treatment and tapering protocol as well as whether CSs are more effective in patients with certain phenotypes.

Immunosuppressives

Immunosuppressives are a group of drugs acting by inhibiting proliferation and activation of lymphocytes. In recent years the experience with AZ, 6-mercaptopurine (6-MP), methotrexate, cyclosporin, and tacrolimus has increased considerably. AZ is a prodrug that is converted to 6-MP. Subsequently 6-MP can be metabolized by thiopurine methyltransferase to an inactive metabolite, 6-methylmercaptopurine, or can be anabolized to two active metabolites, 6-thioguanine and 6-methylmeracaptopurine ribonucleotides. The therapeutic efficacy and the side-effects of AZ are related to the serum levels of 6-thioguanine. A genetic polymorphism for thiopurine methyltransferase influences its activity. Low levels of thiopurine methyltransferase activity are associated with increased levels of 6-thioguanine, thus increasing both therapeutic efficacy and toxicity.

Azathioprine and 6-mercaptopurine

The optimal dose of AZ is 2 to 2.5 mg/kg bodyweight and of 6-MP 1 to 1.5 mg/kg bodyweight. The favorable results of the drug could appear after several (12 or more) weeks.

A recent analysis of eight randomized trials revealed that AZ and 6-MP were effective for inducing remission in active CD. Treatment longer than 17 weeks resulted in a better outcome. A steroid sparing effect was also seen. Adverse events requiring withdrawal from a trial were increased with active therapy.24

AZ and 6-MP are considered to be effective in approximately 40% of IBD patients after 5 years of treatment. According to recent data, one-quarter of the patients discontinued the drugs within 3 months, due to adverse events. If the results are favorable in the first months, the use of AZ could be extended over many years.25 It must be stressed that AZ withdrawal is associated with a high risk of relapse. If AZ is well tolerated, it should not be interrupted.26 Most experts agree that the concurrent use of mesalazine and AZ as induction or maintenance treatment in patients with IBD is justified. According to recent data the concomitant use of aminosalicylates and AZ offer much benefit to the patient.27

Methotrexate

Experience with methotrexate is much less than with AZ. It can be used in patients with steroid-dependent or steroid-refractory CD for induction as well as maintenance of remission.28 Optimal dose and mode of application are still a matter of debate. The usual dose is 25 mg/week for induction and 15 to 25 mg/week for maintenance of remission, both applied subcutaneously (sc) or intramuscularly.29

In everyday clinical practice methotrexate is used mainly in patients who have failed treatment with AZ or who are intolerant to AZ and 6-MP. The effectiveness of the drug in fistulizing CD is weak. An old study did not prove that methotrexate is efficacious in UC patients.30 Current guidelines do not recommend its use in patients with UC.

Tacrolimus

Tacrolimus is a calcineurin inhibitor that suppresses pro-inflammatory cytokine production and T-cell activation. Side effects, such as nephrotoxicity, are dose-dependent although reversible with dose reduction or cessation of therapy.

The drug has been used in patients with fistulizing CD and refractory UC. Long-term administration seems to be an effective and well-tolerated treatment for patients with refractory UC.31 However, the reported results should be interpreted with caution due to the small number of patients treated. Topical tacrolimus has also been used to treat pyoderma gangrenosum and ulcerative proctitis with good results.32

In general, tacrolimus is a well-tolerated and useful drug that should be considered as an alternative agent in the treatment of IBD, especially in those who are intolerant or refractory to conventional immunosuppressives.33 However, more data are needed to determine the long-term efficacy and safety of tacrolimus.

Cyclosporin

Cyclosporin is a powerful immunosuppressive drug mainly used for the prevention of rejection in transplant patients. The drug has been used in patients with severe flare-ups of UC not responding to conventional treatment. Treatment with intravenous (iv) cyclosporin helps to avoid colectomy in a substantial proportion of patients with severe UC.34 In a relevant study in which iv cyclosporin at a dose of 5 mg/kg was administered to 18 patients with fulminant UC, 83% of patients responded to treatment. On follow-up at 2, 6, 12, and 24 months, the colectomy-free rates were 72%, 67%, 61%, and 56%, respectively.35

The mechanisms of action of the drug are not yet fully understood. Cyclosporin was shown in experimental colitis to upregulate the expression of TGF-β in the colonic tissue, enhance the expression of p-Smad2 and cFLIP in epithelial cells, and inhibit caspase-8 activity, concurrently protecting from epithelial apoptosis associated with upregulation of TGF-β-related signaling.36

The adverse events are mild in most patients. However some adverse effects could be dangerous. The clinician must always follow up the patient appropriately by checking regularly drug serum levels.

Side-effects of immunosuppressives

In clinical practice AZ or 6-MP are not effective in one-third of patients. Up to 20% of patients discontinue therapy due to side-effects. Monitoring side-effects of immunosuppressives is mandatory for physicians treating IBD patients.

Thioguanins may have severe side-effects, the most important being various gastrointestinal symptoms, hepatotoxicity, and pancreatitis. Nodular regenerative hyperplasia is another important side-effect especially in men with CD after ileocecal resection. Methotrexate can induce myelosuppression, pulmonary fibrosis, and hepatic injury. Five milligrams of folic acid per week decreases gastrointestinal side effects without interfering with drug efficacy. Cyclosporin can cause renal dysfunction, tremor, hirsutism, hypertension, gum hyperplasia as well as gastrointestinal side-effects such as diarrhea, nausea, vomiting, hepatic disease, and, rarely, gastritis, and peptic ulcer.37

A trial of 6-MP should be considered in AZ intolerance, as half the patients tolerate a switch to 6-MP. Patients with hepatotoxicity or arthralgias and myalgias during AZ treatment might benefit more often than those with other types of adverse events.38 Allopurinol has been shown to reduce the metabolism of both AZ and 6-MP. The drug has been used along with reduced-dose thiopurine in an attempt to avoid adverse drug reactions.39

Conclusion

AZ and 6-MP are effective drugs for inducing remission in patients with active CD as well as for the maintenance of remission. The rate of response increases after 17 weeks of therapy. Recent data support the safety of AZ and 6-MP use in pregnancy and lactation. Thiopurine therapy in IBD is associated with an increased risk of lymphoproliferative disorders. AZ and 6-MP remain among the mainstays of IBD therapy.

Antibiotics

The rationale for using antibiotics in the treatment of IBD is based on the assumption that intestinal bacteria are involved in the pathogenesis of the disease. The terminal ileum and large bowel represent the areas most frequently affected by IBD and concurrently represent the sites with the highest bacterial concentrations. Pouchitis seems to be associated with bacterial overgrowth and dysbiosis.

Enteric flora is altered in patients with IBD and enteric bacteria can be found within the inflamed mucosa. There are indications suggesting that immunological tolerance to commensal bacteria has been lost in patients with IBD. Increased numbers of bacteroides, Escherichia coli, and enterococci, and decreased numbers of lactobacilli and bifidobacteria have been found in IBD patients. Finally, strong evidence from animal models suggests that the development of colitis is impossible in the absence of normal enteric flora. All these data support the assumption that manipulation of intestinal microbiota flora, with either antibiotics or probiotics, could be of benefit in patients with IBD.

Early studies claimed that a decrease in the mucosal peptide antibiotics (defensins) could be involved in the pathogenesis of IBD. Defensins are antimicrobial peptides produced at a variety of epithelial surfaces. Their main function is to maintain a balance between protection from pathogens and tolerance to normal flora. It has been suggested that attenuated expression of defensins compromises host immunity, thus altering the balance in favor of inflammation. This deficient induction may be due to changes in the intracellular transcription by NF-κB and the intracellular peptidoglycan receptor NOD2.40 The beneficial effect of antibiotics in CD patients supports the assumption of the existence of an impaired mucosal antibacterial activity.41 However, recent reports suggest that defensin deficiency might be a consequence of mucosal surface destruction due to inflammatory process rather than a primary event, indicating that reduced defensin expression represents a consequence of the disease and not the real cause.42 Additional research is required in order to further clarify this interesting subject.

Antibiotics in ulcerative colitis

To date, relatively few trials on the use of antibacterial agents in UC patients have been carried out. Despite the fact that the results of these studies are not conclusive most clinicians have used antibiotics as an adjuvant therapy for severe UC.

Older studies showed that iv metronidazole in conjunction with CSs produced no better results compared with placebo plus CSs in inducing remission in patients with severe UC.43 It was reported that 74% of patients with acute relapse of UC who received CSs plus oral tobramycin achieved complete symptomatic remission while significantly fewer (43%) patients who received CSs plus placebo achieved remission.44

Ciprofloxacin has also been tried in patients with UC with disappointing results.45 In order to overcome the disadvantages of their previous study on the route, duration, and dose of ciprofloxacin, the same authors described that iv ciprofloxacin was not effective as an adjunctive treatment to CSs in severe UC.46

Rifaximin was also investigated in patients with moderate-to-severe active UC refractory to steroid treatment. Patients received either rifaximin 400 mg twice daily or placebo for 10 days as an adjunct to steroid treatment. No significant differences in clinical efficacy were found, although rifaximin significantly improved stool frequency, rectal bleeding, and sigmoidoscopic score.47

Two recently published studies have reported that combination treatment with antibiotics offers significant benefit in patients with active UC. In the first study the authors enrolled 25 patients. Patients received amoxicillin 500 mg three times daily, tetracycline 500 mg three times daily and metronidazole 250 mg three times daily for 2 weeks as well as conventional treatment. At 3 and 12 months after antibiotic treatment, clinical activity indexes, and endoscopic and histological scores were significantly decreased compared with those before treatment. The clinical response rates in steroid-dependent patients were 60% and 73.3% at 3 and 12 months, respectively, and 50% at 12 months in steroid-refractory patients. Among the steroid-dependent or refractory patients, 70.6% discontinued steroid therapy at 12 months. No serious drug-related toxicities were observed.48 In the second trial the authors investigated whether antibiotic combination induces and/or maintains remission of active UC. Patients with mild-to-severe relapsing UC were assigned to oral amoxicillin 1500 mg/day, tetracycline 1500 mg/day, and metronidazole 750 mg/day, versus placebo, for 2 weeks, and then followed up. This 2-week triple antibiotic therapy produced improvement, remission, and steroid withdrawal in active UC more effectively than the placebo.49

It seems that the subject of the role of antibiotics in UC is still open and further studies are required to better clarify their role in both active and inactive UC.

Antibiotics in Crohn’s disease

During recent years an increased amount of research has been published on the use of broad-spectrum antibiotics in CD patients. The antibiotics used so far in patients with CD include metronidazole, ornidazole, ciprofloxacin, tobramycin, clarithromycin, cotrimoxazole, and anti-TB treatment.

Metronidazole

Metronidazole has been investigated from the early 1970s. In a study conducted to test the efficacy and safety of the drug in CD patients, it was found that there was no difference between metronidazole and placebo-treated patients although a positive trend in favor of metronidazole was observed in patients with Crohn’s colitis.50 In the National Cooperative Swedish Study, metronidazole was compared with sulfasalazine as a primary treatment for CD. Although no significant difference was found between the two groups, metronidazole was effective in patients who fail to respond to sulfasalazine.51

In another study, metronidazole was used either as a single therapy or in combination with cotrimoxazole and compared with cotrimoxazole alone and a double placebo in patients with a symptomatic relapse of CD. After 4 weeks’ treatment there was no difference in response among the three treatment groups.52 In a subsequent study treatment with metronidazole for 16 weeks significantly decreased the CDAI, but no difference was found in the rates of remission compared with placebo.53

The potential for metronidazole 10% ointment to exert therapeutic benefit in perianal CD was recently evaluated. Patients received metronidazole 10% ointment, 0.7 g applied perianally three times daily, or placebo ointment. The mean reduction in perianal CD activity index score at 4 weeks did not differ between the two groups. However, more patients in the metronidazole group showed a reduction in Pediatric Crohn’s Disease Activity Index of at least five points compared with the placebo group. Perianal discharge and perianal pain both declined significantly in the metronidazole-treated patients. Metronidazole 10% ointment was well tolerated, with minimal adverse effects. It could be used as a potential treatment for pain and discharge associated with perianal CD.54

Metronidazole has also been used in combination with other antibiotics. An antibiotic combination including 250 mg metronidazole four times daily plus 500 mg ciprofloxacin twice daily was compared with a standard steroid treatment for 12 weeks. The 2 treatments showed similar rates of remission, suggesting that this combination is a potential alternative to steroid treatment in the acute phase of CD.55 In another trial the combination of metronidazole and ciprofloxacin was supplemented with budesonide (9 mg/day) for active CD. No difference was noticed compared with placebo, but the overall response in the two groups was lower than that in previous studies using budesonide, suggesting that antibiotic treatment is more effective in colonic disease than in isolated small bowel involvement.56

Unfortunately, the systematic administration of metronidazole is accompanied by important side-effects, including nausea, anorexia, dysgeusia, dyspepsia, and peripheral neuropathy, which limit its use in approximately 20% of patients.

Ornidazole

Ornidazole is a nitroimidazole derivate with a similar chemical structure and antimicrobial properties to metronidazole. Initially the efficacy of the drug was tested in a small number of patients with active CD.57 In a subsequent study, 25 patients with active CD received 500 mg/day of ornidazole for 4 weeks.58 The results showed that the Crohn’s Disease Activity Index (CDAI) declined significantly from week 0 to week 4, while the number of patients going into remission increased gradually from week 0 to week 4. Presence and severity of abdominal pain decreased and bowel movements were reduced. General well-being improved significantly. An increase in bodyweight was noticed at the end of the fourth week. The drug also seems to reduce the recurrence rate,59 while being quite safe.60 In normal subjects ornidazole reduces the levels of serum C3.61

Ciprofloxacin

Ciprofloxacin has been extensively used in patients with active CD with or without perineal involvement. In a study comparing ciprofloxacin 500 mg twice daily with placebo twice daily for 6 months, the administration of ciprofloxacin significantly reduced CDAI score compared with placebo.62 In another study patients with a mild-to-moderate flare-up of CD were randomized to receive ciprofloxacin 1 g/day or mesalazine (Pentasa®; Shire) 4 g/day for 6 weeks. Complete remission was observed in 56% of patients treated with ciprofloxacin and in 55% of those treated with mesalazine.63 In an open study 72 patients with active CD were treated with ciprofloxacin 500 mg twice daily and metronidazole 250 mg three times daily for 10 weeks. Clinical remission was observed in 68% of patients, and 76% showed clinical response.64

The drug has also been used in patients with fistulizing disease. In a relevant study, 25 patients with CD and actively draining perianal fistulas received ciprofloxacin 500 mg, metronidazole 500 mg, or placebo twice daily for 10 weeks. Remission and response was more frequent in patients treated with ciprofloxacin although the differences were not significant.65

Ciprofloxacin is an effective drug in a proportion of patients with active CD mainly located in the colon.

Clarithromycin

Clarithromycin is a broad-spectrum antibiotic that has good penetration into macrophages. Clarithromycin 1 g for 3 months was found to be ineffective in active CD although benefit was observed during the first month, suggesting that an initial effect may be attenuated by subsequent bacterial resistance.66

Rifaximin

Rifaximin is a rifamycin analog with a broad spectrum of activity. The drug has been used mainly on intestinal infections because it is an almost non-absorbed antibiotic from the gastrointestinal tract.

In an open-label study on the efficacy and safety of rifaximin 600 mg/day for 16 weeks in patients with mild-to-moderate active CD, 59% of patients were in remission at the end of the study, with a significant reduction of the mean CDAI score compared with baseline.67

In another study patients with mild-to-moderate CD were randomized to three treatments for 12 weeks: rifaximin 800 mg once daily plus placebo, rifaximin 800 mg twice daily, and placebo twice daily. Remission and response rates of rifaximin 800 mg twice daily were significantly higher than those of placebo and rifaximin 800 mg once daily in patients with elevated C-reactive protein (CRP) values. Rifaximin 800 mg twice daily was superior to placebo in inducing clinical remission.68

A recent experimental study suggested that the preventive and therapeutic role of rifaximin on IBD is probably achieved through human pregnane X receptor-mediated inhibition of the NF-κB signaling cascade.69

Anti-TB treatment

It has been suspected that Mycobacterium avium subsp. paratuberculosis, which causes Johne’s disease, might also be a cause of CD.

In a prospective, parallel, placebo-controlled, double-blind, randomized trial of 2 years duration, 213 patients with active CD were randomized to clarithromycin 750 mg/day, rifabutin 450 mg/day, clofazimine 50 mg/day or placebo, in addition to a 16-week tapering course of prednisolone. At week 16, there were significantly more subjects in remission in the antibiotic arm (66%) than the placebo arm (50%). During the following year, no significant differences between antibiotic and placebo groups were noticed. The findings of this study do not support a significant role for M. avium subsp. paratuberculosis in the pathogenesis of CD in most patients.70

Prevention of postoperative recurrence by antibiotics

Antibiotics have also been studied in the prevention of postoperative disease recurrence of CD. Sixty patients were randomized to receive either metronidazole or placebo for 12 weeks. Metronidazole significantly reduced the incidence of severe endoscopic relapse and clinical recurrence rate.71 More recently, ornidazole used continuously for 1 year was shown to be more effective than placebo in the prevention of clinical and endoscopic recurrence in the neoterminal ileum.72

A recent study investigated whether metronidazole for 3 months together with AZ for 12 months was superior to metronidazole alone in reducing recurrence of postoperative CD in high-risk patients. Despite the enhanced risk of recurrence, the overall incidence of significant recurrence was rather low, probably owing to metronidazole treatment. Concomitant AZ resulted in lower endoscopic recurrence rates and less severe recurrences.73 Therefore this combined treatment seems to be reasonable for postoperative CD patients with an enhanced risk for recurrence.

The results of reported studies suggest that antibiotics are useful in the treatment of patients with CD. According to the opinion of many experts, incorporation of antibiotics into the therapeutic armamentarium for CD either as first-line therapy or in combination with immunosuppressive drugs might be a rational strategy.74 This assumption is further supported by the results of a recent meta-analysis which showed that long-term treatment with nitroimidazoles or clofazimine are effective in patients with CD.75

However significant questions remain to be answered. Why are only a small number of antibiotics useful in patients with IBD? What is the exact mode of action of metronidazole and ciprofloxacin? What is the role of concurrent infection (eg, Yersinia enterocolitica) in the course of CD? (We must bear in mind that ciprofloxacin is an effective drug against Yersinia spp.). In the near future, the answers to these questions could result in a more etiological therapeutic approach.

Probiotics

Probiotics are live non-pathogenic microorganisms administered to improve microbial balance in the gastrointestinal tract. They consist of Saccharomyces boulardii yeast or lactic acid bacteria, such as Lactobacillus and Bifidobacterium spp.

Probiotics exert their beneficial effects through various mechanisms, including reduced intestinal pH, decreased colonization and invasion by pathogenic organisms, and modification of the host immune response. Lactobacillus paracasei significantly decreases the plasma and lymphocyte content of proinflammatory cytokines in patients with UC.76 S. boulardii-secreted protein(s) inhibit production of proinflammatory cytokines by interfering with the global mediator of inflammation NF-κB, and modulating the activity of the mitogen-activated protein kinases ERK1/2 and p38. It has also some other interesting properties, including activation of expression of PPAR-γ, suppression of ‘bacteria overgrowth’ and host cell adherence, release of protease that cleaves Clostridium difficile toxin A, and stimulation of antibody production against toxin A.77

We must bear in mind, however, that probiotic benefits associated with one species or strain do not necessarily hold true for others. Also there is no consensus about the number of microorganisms that must be ingested to obtain a beneficial effect; however, a probiotic should typically contain several billion microorganisms to increase the chance of adequate gut colonization.78

Probiotics in ulcerative colitis

The administration of probiotics in patients with UC seems to be quite beneficial. The induction of remission in patients with active distal UC by E. coli Nissle (EcN) administered in the form of enemas was investigated in a recent clinical trial. Patients were assigned to treatment with 40, 20, or 10 mL enemas containing 10E8 EcN/mL or placebo once a day for 2 weeks. In the intention-to-treat analysis the number of responders was not significantly higher in the EcN group than in the placebo group, although the efficacy of rectal EcN was significant in the per-protocol analysis.79 The results support EcN as a well-tolerated alternative treatment in moderately active distal UC.

The use of probiotics in UC patients to maintain remission seems to be promising. VSL#3® (Sigma-Tau Pharmaceutics, Inc, Gaithersburg, MD) was shown to be a safe and effective modality in achieving clinical responses and remissions in patients with mild-to-moderately active UC.80 In a relevant study it was reported that the decrease in UC activity index scores (UCDAI) of 50% or more was significantly higher in the VSL#3 group than in the placebo group (63.1 versus 40.8). Significant improvement with VSL#3 in the UCDAI score and the degree of rectal bleeding was recorded. Remission rate was significantly higher in the VSL#3 group than in the placebo group (47.7% versus 32.4%). VSL#3 supplementation seems to be safe and able to reduce UCDAI score in patients with relapsing mild-to-moderate UC who are under treatment with mesalazine and/or immunosuppressants.81

Rembacken et al investigated whether the administration of a non-pathogenic strain of EcN was as effective as mesalazine in preventing relapse of UC as well as whether the addition of E. coli to standard medical therapy increased the rate of remission of active UC. The results showed that 75% of patients in the mesalazine group achieved remission compared with 68% in the E. coli group. In the mesalazine group, 73% of patients relapsed compared with 67% in the E. coli group (no significant differences).82 They concluded that treatment with a non-pathogenic E. coli is equally effective as mesalazine in maintaining remission of UC.

Lactobacillus rhamnosus GG strain alone or in combination with mesalazine decreased the relapse rate and significantly increased time to relapse compared to mesalazine alone. Bifidobacteria-fermented milk-supplemented patients with UC had significantly fewer exacerbations than non-supplemented patients.83

Probiotics in Crohn’s disease

CD is characterized by increased intestinal permeability that permits antigen penetration into the intestinal tissue. In CD patients in remission, S. boulardii added to baseline therapy may improve the intestinal permeability.84 So far, none of the probiotics tested has been shown to be effective in induction of remission or in maintenance of remission in patients with CD.

Probiotics in pouchitis

Probiotics are probably useful in inducing remission in active pouchitis. In a Cochrane systematic review it was suggested that oral probiotic therapy with VSL#3 appears to be an effective therapy for maintaining remission in patients with chronic pouchitis in remission.85 However, because of the small number of patients tested the results must be interpreted with caution.

A multispecies probiotic mixture of eight strains seems to be helpful in maintaining remission in patients with pouchitis.86

Although probiotics are considered to be well tolerated, some adverse events, mainly bloating and flatulence, can occur. They should be used cautiously in patients who are critically ill or severely immunocompromised or in those with central venous catheters, since systemic infections may rarely occur.87 Administration of bacteria-derived probiotics should be separated from antibiotics by at least 2 hours. Because of the relatively small number of published trials, questions about optimal probiotic, optimal dosing, and specific patient populations to maintain remission remain to be answered.

Biologic agents

Tumor necrosis factor alpha blocking strategies

Because anti-TNF-α plays a pivotal role in the process of the inflammation in IBD patients, inhibition of this cytokine is expected to be a powerful treatment strategy in patients with both CD and UC. The available anti-TNF-α factors include infliximab, adalimumab, and certolizumab pegol. All these factors have been approved for use in the United States; however only the first two are licensed for use in Europe. All major gastroenterological associations recommend that treatment with anti-TNF-α monoclonal antibodies be considered in patients with moderate-to-severe CD refractory to concomitant aminosalicylates, CSs, or immunosuppressives, or patients who have contraindications to, or poor tolerance of, these agents. Infliximab has also been approved for the treatment of patients with severe UC not responding to conservative treatment.

Infliximab

Infliximab (IFX) has successfully been used in patients with CD or UC (Table 2).

Table 2

Infliximab in either Crohn’s disease or ulcerative colitis

Study	Number of patients	Treatment schedule	Primary end-point	Response to treatment
Accent I88	n = 573 active CD	5 mg/kg single infusion5 or 10 mg/kg maintenance for those responded	CDAI > 70 points 2 weeks response clinical remission 54 weeks	58%28.3% and 38.4% respectively vs 13.6% of placebo
Accent II93	n = 306Fistulizing CD	5 mg/kg for those who responded	Week 54 absence of fistulas	36%
Ruggiero160	n = 24 patients with ileocolonic resection	iv 5 mg/kg for 12 months vs placebo	Endoscopic and histologic recurrence at 1 year	91% and 27.3% (Infliximab) vs 84.6% and 84.6% (placebo)
Colombel94	n = 508 patients with moderate-severe CD	5 mg infliximab/kg at weeks0, 2, and 6 and then every 8 weeks plus daily oral placebo vs 2.5 mg oral azathioprine/kg daily plus a placebo infusion vs combination of the 2 drugs.	Corticosteroid-free clinical remission at week 26	56.8% (IFX plus AZ) vs 44.4% (IFX + placebo) vs 30.0% (AZ) (significant differences)
Kohn99	n = 83 patients with severe UC	Infliximab 5 mg/kg iv (1 or more infusions)	Short-term outcome: colectomy/death 2 months after the first infusion.Long-term outcome: survival free from colectomy	15% underwent colectomy after first infusion (greater rates in patients receiving only 1 infusion)
ACT 1 and ACT 2 studies96	n = 364 patients with UC and Mayo score 6–12	Placebo vs infliximab (5 or 10 mg/kg) at weeks 0, 2, and 6, then 5 mg/kg/8 weeks through week 46 (ACT 1) or through week 22 (ACT 2)	Response: drop of Mayo >3 rectal bleeding: 0–1
			ACT 1
			Response week 8	69%
			Response week 54	45%
			ACT 2
			Response week 8	64%
			Response week 30	31%

Abbreviations: AZ, azathioprine; CD, Crohn’s disease; CDAI, Crohn’s disease activity index; IFX, infliximab; UC, ulcerative colitis.

Infliximab in Crohn’s disease

IFX is an immunoglobulin G1 (IgG1) type chimeric monoclonal antibody against TNF-α which acts by binding to circulating and membrane-bound TNF-α, inducing a cell mediated cytotoxic reaction and enhancing the programmed cell death of activated T-cells.

Studies on the use of IFX in either CD or UC are shown in Table 2. The ACCENT I study showed that treatment should be maintained in patients who responded to a single infusion of IFX88 and that maintenance therapy is superior to episodic administration while providing less anti-IFX antibody formation.89 Patients receiving systematic therapy also need fewer hospitalizations and less surgery.90

Healing of the mucosa has been shown to be a strong predictor of improved outcome of CD and anti-TNF-α therapy is a strong inducer of mucosal healing.91

IFX is also efficacious in fistulizing CD. In the study of Present et al, the primary end-point (a reduction of 50% or more from baseline in the number of draining fistulas) was achieved in 68% and 56% of patients treated with 5 and 10 mg/kg IFX at week 0, 2, and 6, compared with 13% of the patients receiving placebo. The secondary end-point (closure of all fistulas) was achieved in 55% of the patients assigned to receive 5 mg/kg of IFX and 38% of those assigned to 10 mg/kg compared with 13% of patients receiving placebo (P = 0.002 and P = 0.02, respectively).92

The ACCENT II study demonstrated the efficacy of IFX in maintaining the good results in patients with perianal and enterocutaneous fistulae. The median time during which the patients were in remission was 14 and 40 weeks in the placebo and IFX groups, respectively. The remission rate was 36% in the IFX group compared with 19% in the placebo group.93

In a recent trial, the efficacy of IFX monotherapy, AZ monotherapy, and the two drugs combined was tested in 508 adults with moderate-to-severe CD. These patients had not undergone previous immunosuppressive or biologic therapy. Patients who were treated with IFX plus AZ or IFX monotherapy were more likely to have a corticosteroid-free clinical remission than those receiving AZ monotherapy.94

Timing of biological therapy is a matter of continuous debate. Early aggressive immunosupression seems to be the most efficacious therapeutic strategy in high-risk patients. In a meta-analysis it was found that early diagnosis, need for CS therapy at the first flare, and fistulizing behavior at the time of the diagnosis were independent risk factors for an unfavorable disease course.95 Extended small bowel disease, upper gastrointestinal involvement, and smoking, also seem to represent risk factors for an unfavorable course.

Infliximab in ulcerative colitis

Two randomized, double-blind, placebo-controlled studies (ACT 1 and ACT 2), evaluated the efficacy of IFX for induction and maintenance therapy in patients with UC. Patients with a Mayo score of 6 to 12 points and moderate-to-severe active disease on sigmoidoscopy despite concurrent treatment with CSs alone or in combination with AZ or 6-MP in ACT 1 or despite concurrent treatment with CSs alone or in combination with AZ or 6-MP and mesalazine in ACT 2, were investigated. In ACT 1, 69% and 61% of patients who received 5 or 10 mg/kg of IFX had a clinical response at week 8, compared with 37% of those who received placebo. In ACT 2, clinical response at week 8 was noticed in 64% and 69% of patients who received 5 or 10 mg/kg of IFX compared with 29% of those on placebo.96

The efficacy of IFX as a rescue therapy for severe to moderately severe UC not responding to iv steroid therapy has also been documented. In a relevant study significantly more patients treated with placebo required colectomy by 3 months compared with those treated with a single infusion of 5 mg/kg IFX.97 Patients with moderate-to-severe UC treated with IFX were significantly less likely to undergo colectomy through 54 weeks than those receiving placebo.98 In the short term, two or more infusions seem to be more effective than a single infusion.99

Adalimumab

Adalimumab (ADA) is a fully human IgG1 type anti-TNFα monoclonal antibody that it is administered subcutaneously.

The CLASSIC-I trial investigated the efficacy of ADA for induction of remission in patients with CD.100 A total of 299 patients with moderate to severe CD naive to anti-TNF therapy received ADA 40 mg/20 mg, 80 mg/40 mg, or 160 mg/80 mg or placebo at weeks 0 and 2. The rates of remission at week 4 in the ADA 40 mg/20 mg, 80 mg/40 mg, and 160 mg/80 mg groups were 18%, 24% and 36%, respectively, in comparison with 12% in the placebo group. It was confirmed in this study that the optimal induction dosing regimen for ADA is 160 mg at week 0 followed by 80 mg at week 2 (Table 3).

Table 3

Adalimumab in either Crohn’s disease or ulcerative colitis

Study	Number of patients	Duration of treatment	Comparisons	Primary end-point	Response to treatment
CHARM study102	n = 778	3–12 months	Placebo vs adalimumab40 mg eow vs adalimumab40 mg weekly, all after an 80 mg/40 mg adalimumab induction regimen	3- and 12-month hospitalization risks	Less rates of hospitalization and CD-related operations in adalimumab group
CLASSIC-I100	Moderate to severe CD n = 299	Adalimumab sc 160 and 80 mg or 80 and 40 mg or 40 and 20 mg at week 0 and 2		Remission rate at week 4	36%24%18%
CLASSIC-II101	Patients from Classic I n = 276	40 mg: week 0 and 2 and maintenance therapy40 mg eow or weekly until week 56		Remission rates	79%83%
Colombel106	n = 117	56 weeks	After induction treatment patients at week 4, were assigned to double-blind placebo or adalimumab40 mg eow or weekly to week 56	Healing of draining fistulas in patients with active CD	Mean number of draining fistulas/d significantly decreased in adalimumab-treated patients
Sandborn103	Loss of response to IFX n = 325	4-week, double-blind, placebo	160 mg and 80 mg at weeks 0 and 2	Remission at week 4 response	21% in the adalimumab vs 7% of placebo.70-point response: 52% in adalimumab vs 34% of placebo
Triantafillidis104	n = 30	Patients either naive to biologics or with response loss or intolerance to IFX			Remission in 63.3%Clinical response in 30%
Reinisch107	n = 390 with UC	8 weeks	Adalimumab (160/80 or 80/40) vs placebo	Clinical remission	18.5% vs 9.2% (P = 0.031)10% vs 9.2% (NS)

Abbreviations: CD, Crohn’s disease; eow, every other week; IFX, infliximab; UC, ulcerative colitis.

The CLASSIC-II study evaluated the long-term efficacy and safety of ADA.101 Patients from CLASSIC-I study (n = 276) were included and received open-label ADA 40 mg at week 0 (week 4 of CLASSIC I) and week 2. Patients in remission at week 0 and 4 were re-randomized to ADA 40 mg weekly or every other week (eow) or placebo until week 56. Non-remitting patients were randomized to open-label 40 mg ADA eow Fifty-five of 276 patients achieved remission at week 4; 79% who received ADA 40 mg eow and 83% who received 40 mg weekly were in remission at week 56, versus 44% for placebo. Of 204 patients who entered the open-label arm, 46% were in clinical remission at week 56. Therefore, these two studies revealed that ADA is able to induce and maintain remission in CD patients.

A larger study (CHARM) evaluated the efficacy of adalimumab in the maintenance of response in 854 CD patients.102 After an open-label induction therapy with 80 mg (week 0) and 40 mg (week 2) patients were randomized to 40 mg ADA eow, 40 mg ADA weekly or placebo maintenance therapy. The percentage in remission was significantly greater in the ADA 40-mg eow and 40-mg weekly groups versus placebo at week 26 (40%, 47%, and 17%, respectively) and week 56 (36%, 41%, and 12%, respectively).

ADA induces remissions more frequently than placebo in adult patients with CD who cannot tolerate IFX or are symptomatic despite receiving IFX therapy.103 In a relevant study 21% of patients in the ADA group versus 7% of those in the placebo group achieved remission at week 4. A 70-point response occurred at week 4 in 52% of patients in the ADA group versus 34% of patients in the placebo group. Therefore, ADA is well tolerated and appears to be a beneficial option for patients with CD who have lost their response to or cannot tolerate IFX, for non-smokers, for patients with short duration of CD, and for patients with extraintestinal manifestations who have a better clinical response.104 Moreover, patients with moderate-to-severe CD treated with ADA had lower 1-year risks of hospitalization and surgery than placebo patients.105

ADA has also excellent results in healing of draining fistulas in patients with active CD.106 It was found that the mean number of draining fistulas per day was significantly decreased in ADA-treated patients compared with placebo-treated patients. ADA therapy was more effective than placebo for inducing fistula healing and complete fistula healing was sustained for up to 2 years by most patients.

Adalimumab in ulcerative colitis

The results on efficacy and safety of ADA for the induction of remission in anti-TNF naive patients with moderately to severely active UC were recently published.107 In this study 18.5% of patients in the ADA 160 mg/80 mg group (P = 0.031 versus placebo) and 10.0% in the ADA 80 mg/40 mg group (P = 0.833 versus placebo) were in remission at week 8, compared with 9.2% in the placebo group. Serious adverse events occurred in 7.6%, 3.8% and 4.0% of patients in the placebo, ADA 80 mg/40 mg, and ADA 160 mg/80 mg groups, respectively. ADA was safe and effective for induction of clinical remission in patients with moderate to severely active UC failing treatment with CSs and/or immunosuppressants.

The efficacy of ADA in patients with UC who lost the response or became intolerant to IFX was also studied in a small number of patients.108 In an open-label study, ADA induction therapy with 160 mg/80 mg resulted in remission at week 4 in four out of ten patients while three other patients improved.

In a more recent study on patients with UC who lost response to IFX, ADA achieved clinical response at weeks 4 and 12 in 53% and 60% of patients, respectively, and clinical remission in 10% and 27% of patients, respectively. After a mean 48-week follow-up, 50% of patients continued on ADA. All patients who achieved clinical response at week 12 were colectomy free in the long term.109

Certolizumab pegol

Certolizumab pegol (CZP) is an antigen-binding fragment (Fab’) portion of an IgG antibody attached to a 40-kDa polyethylene glycol moiety to increase the t1/2 of the treatment to approximately 2 weeks. The drug has been approved in the United States for use in patients with CD not responding to conventional treatment, while in Europe it is approved only in Switzerland for the treatment of CD (Table 4).

Table 4

Certolizumab in Crohn’s disease

Study	Number of patients	Duration of treatment	Comparisons	Primary end-point	Response to treatment
Schreiber118PRECiSE 2 subpopulation	CZP n = 28Fistulizing diseasePlacebo n = 30	26 weeks	CZP vs placebo	closure of fistula	36% vs 17% (P = 0.038)
Schoepfer117	n = 50	6 weeks	CZP 400 mg sc at weeks 0, 2, and 4	Response and remission rates	Response = 54%Remission = 40%Effectiveness in fistulizing disease
Schreiber112	n = 428	26 weeks	Induction therapy, 400 mg CZP at weeks0, 2, and 4. Patients with clinical response received 400 mg CZP or placebo/4 weeks through week 24	Maintenance of response through week 26. BaselineCRP > 10 mg/L	Response was maintained through week 26 in 62% of CZP vs 34% of placebo, P < 0.001)Among patients with response to induction therapy remission at week 26 was seen in 48% of CZP vs 29% of placebo (P < 0.001).
Sandborn111	n = 662		Patients were stratified according to baseline CRP. Treatment: either 400 mg of CZP or placebo at weeks 0, 2, and 4 and then every 4 weeks		Patients with CRP >10 mg: 37% in CZP group had response at week 6, vs 26% in the placebo group (P = 0.04).At weeks 6 and 26, the corresponding values were 22% and 12% (P = 0.05). Overall, response rates at week 6: 35% in CZP vs 27% in placebo (P = 0.02)

Abbreviations: CRP, C-reactive protein; CZP, certolizumab pegol.

A phase II trial demonstrated the efficacy of a 400 mg sc dose of the drug.110 Subsequently, the efficacy of CZP was evaluated in two studies (PRECiSE 1 and 2). Patients with moderate-to-severe CD (n = 662) were randomly assigned to 400 mg CZP or placebo at weeks 0, 2, and 4.111 Maintenance therapy was administered every 4 weeks. Induction of remission as a primary end-point was evaluated at weeks 6 and 26. Response rates were higher in the CZP group than in the placebo group at both time points (35% versus 27% and 23% versus 16%, respectively). Patients with elevated CRP levels showed a more pronounced improvement.

In the PRECiSE 2 study the efficacy of maintenance therapy in 668 patients with moderate-to-severe CD was evaluated.112 Maintenance of response was significantly higher in the active treatment group (63% versus 36%).

The PRECiSE 3 study evaluated the long-term results of CZP administration.113 The observational period was 3.5 years. Long-term remission rates were observed in the PRECiSE 3 patients receiving CZP and specifically in patients with no previous exposure to other TNF inhibitors.

The WELCOME study revealed that location of CD, resection, number of resections, and baseline disease activity have a significant impact on the probability of achieving remission after 26 weeks of treatment.114

Evidence for mucosal healing has now been provided for CZP.115 Maintenance therapy with CZP resulted in significant and clinically meaningful improvements in health-related quality of life. Furthermore, a significant proportion of patients who received CZP returned to a normal life compared with those who received placebo.116

In a population of CD patients with perianal disease, CZP induced a response and remission rates in 54% and 40% of patients, respectively. The drug seems to be effective in perianal fistulizing CD.117

Another study examined whether fistula closure is maintained at week 26 after treatment with CZP. It was found that at this time, 36% of patients in the CZP group had 100% fistula closure compared with 17% of patients receiving placebo (P = 0.038). It seems therefore that continuous treatment with CZP improves the likelihood of sustained perianal fistula closure compared with placebo.118

The published controlled trials regarding the use of CZP in the treatment of CD share similar limitations with other studies of TNF-α antagonists including high placebo response, natural course of disease fluctuation, and the use of CDAI to assess outcomes. However, CZP is considered to be an effective agent for adult patients with moderate-to-severe CD. CZP and ADA, unlike IFX, can be self-administered. With similarity in cost and the lack of head-to-head comparisons, patient and physician preference may determine choice of TNF-α antagonist.119

Side-effects of anti-TNF-α factors

The most significant side-effects are related to opportunistic infections, malignancies, as well as injection/infusion reactions and appearance of autoimmunity. Contraindications include the presence of heart failure and acute infectious diseases. Clinicians should be aware that because of the powerful immunosuppressive capacity of biological agents, a rigorous and careful long-term safety follow-up should be adopted for all patients.120

A meta-analysis of anti-TNF trials evaluated the data of 21 studies involving 5356 patients (3341 patients in the anti-TNF groups and 2015 patients in the control groups).121 There was no difference in the frequency of death between the anti-TNF-α and control groups. Overall analysis of anti-TNF trials did not show any differences between anti-TNF-α and control groups in severe infections. Frequency of malignancies did not differ between treated and control groups. An increased number of hepatosplenic T-cell lymphoma in young patients highlighted the question of malignancies in patients treated with TNF-α inhibitors.

Both the US Food and Drug Administration and the European Crohn’s and Colitis Organization categorize anti-TNF agents as safe during pregnancy.122 Live-virus vaccines are generally contraindicated in patients receiving immunosuppressive regimens due to risks of vaccine-associated infection. While patients on immunosuppressives develop immune responses after vaccinations, these may be impaired relative to their non-immunosuppressed counterparts.123

Before starting treatment with biologic agents it is extremely important to assess patients’ prior tuberculosis exposure by performing a tuberculin skin test (Mantoux test) and a chest X-ray, as the use of these biologic agents has been associated with reactivation of a latent tuberculosis. New IFN-γ assays may enhance screening efficacy.

It has been proposed that a Mantoux test in patients with IBD (especially in patients with CD) seems to be meaningless based on the very high incidence of anergy in CD due to the disease itself, treatment with CSs, and poor nutritional status.124

According to data on patients with active UC, the incidence of anergy to the Mantoux test (16%) did not differ from that in normal controls (20%). On the other hand, in patients with active CD the incidence of anergy was significantly lower compared with normal people (20% vs 52%).125

We suggest that a Mantoux test must be performed both in all patients with active IBD, although in patients with CD a negative Mantoux test does not exclude the possibility of latent tuberculosis.126

Prophylaxis regimen will vary from country to country depending on resistance prevalence. In patients with a positive Mantoux test, isoniazide must be administered for 9 months. TNF-α antagonist should be started only after 1 month of treatment with isoniazide. Rifampicin for 4 months has also been suggested although it does not seem as good as an isoniazide regimen. We must bear in mind, however, that patients positive on screening who are treated with isoniazide and subsequently receive biologic agents still have an approximately 19% risk for tuberculosis.127

Postsurgical treatment of patients with Crohn’s disease with biologic agents

CD commonly recurs after intestinal resection. Administration of IFX after intestinal resection for CD is effective in preventing endoscopic and histologic recurrence. In a small trial the rate of endoscopic recurrence at 1 year was significantly lower in the IFX group (1 of 11 patients; 9.1%) than the placebo group (11 of 13 patients; 84.6%).127 Larger studies may be desirable to strengthen the available data.

A thorough understanding of the mechanisms involved in the effectiveness of IFX in the postoperative setting could substantially improve our therapeutic strategies for overall patient management.128

The development of biologic agents and their use in IBD has improved patient quality of life considerably by modifying disease course and preventing complications and surgery. Control of inflammation can be achieved with all three available biologic agents, namely IFX, ADA, and CZP. These agents are effective in both induction and maintenance of remission. For fistula healing, both IFX and ADA are effective. Anti-TNF agents appear to be more effective in patients who have a shorter disease history and who have not yet been treated with any of these agents. Patients with CD who were treated with IFX plus AZ or IFX monotherapy are more likely to have a CS-free clinical remission than those receiving AZ monotherapy. Several strategies can minimize the risks associated with biologic therapies. Proper strategies include careful examination of past history and physical examination and screening for latent tuberculosis. During treatment, patients should be closely monitored. Education of physicians and patients is also important to allow the early detection of any adverse effect.

Emerging therapeutic options for inflammatory bowel disease

During recent years quite a large number of substances have been studied in patients with IBD. Apart from TNF-α inhibitors other molecules such as unfractionated or low-molecular-weight heparin, omega-3 polyunsaturated fatty acids, microbes, and microbial products have been studied. Leucocytapheresis, a method developed and applied mainly in Japan, also seems to be a promising therapeutic strategy.

The emerging therapeutic options for IBD are summarized below.

New and emerging biologic agents

So far, most patients with IBD are treated with rather unspecific medications exerting mainly anti-inflammatory or suppressive effects on the mucosal immune system. Although biologic agents directed against TNF-α represent an effective treatment, 30% of patients with CD will not respond to induction therapy, and of those who initially respond, 50% will cease to respond within a year. During the last decade a better understanding of the underlying pathogenesis of IBD along with great advances in biotechnology has enabled the introduction of many biologic therapies, other than anti-TNF therapies, aiming to act on specific targets.129

We now can target many other proteins or receptors including the protein subunit p40 which heterodimerizes either with p35 resulting in the pro-inflammatory cytokine IL-12 or with p19, thus forming the pro-inflammatory IL-23, as well as antibodies that are able to block adhesion molecules in the areas of inflammation. Multiple genes that have been linked to alterations in immune pathways could also provide ways for understanding the pathogenesis of IBD and suggesting future drug targets.130 Many of these drugs have shown clinical benefit for induction and maintenance therapy in IBD, while others are under evaluation. Experimental data also indicate that pro-inflammatory cytokines play a significant role in promoting tumor development. The anti-cytokine agents could also be efficacious in preventing the onset of inflammation associated colorectal cancer.131

Anti-adhesion (anti-integrin) molecules

IBD is driven by the trafficking of lymphocytes from the circulation into the gut. Several endothelial adhesion molecules including E-selectin, ICAM-1, ICAM-2, VCAM-1, and mucosal addressin Mad-CAM-1, could enhance inflammation by trafficking leucocytes and recruiting immune cells into the gut. These molecules interact with integrins on leukocytes, thus inducing their migration from blood vessels into the site of inflammation.

The adhesion molecules involved represent attractive targets for the development of new drugs, which should aid in reducing existing inflammation and preventing recurrence of inflammation, and may lead to long-term control of disease.132

Natalizumab

Natalizumab is a humanized IgG4 monoclonal antibody that selectively targets the human α4-subunit, thus inhibiting both the VCAM-1/α4β1 and MAdCAM-1/α4β7 pathways of leucocyte adhesion and transmigration. It has been approved for the treatment of patients with moderate-to-severe CD. This drug represents an efficacious therapeutic alternative for patients who do not respond to, or have failed, a TNF-α inhibitor.

In the most significant randomized placebo-controlled trial on the efficacy of natalizumab in CD, 509 patients were allocated to receive either 300 mg natalizumab iv or placebo at weeks 0, 4, and 8. Natalizumab induced response and remission at week 8 that was sustained through week 12. Response and remission rates for natalizumab were superior to those for placebo at weeks 4, 8, and 12, demonstrating the early and sustained efficacy of the drug as induction therapy in patients with elevated CRP and active CD.133 Side-effects did not differ significantly between the two groups, although in the open-label extension of the study, one patient died because of progressive multifocal leukoencephalopathy.

MLN-02

MLN-02 is a humanized IgG1 monoclonal antibody against α4β7 integrin that selectively inhibits leukocyte adhesion in the gastrointestinal mucosa. Also, an Fc receptor recognition and binding has been detected, thus eliminating complement fixation and cytokine release.

In a recent study, patients with active CD were randomized to receive iv MLN-02 2.0 mg/kg, MLN-02 0.5 mg/kg, or placebo on days 1 and 29. Clinical response rates at day 57 were 53%, 49%, and 41% in the MLN-02 2.0 mg/kg, MLN-02 0.5 mg/kg, and placebo groups while clinical remission rates at day 57 were 37%, 30%, and 21%, respectively (P = 0.04 for the 2.0 mg/kg versus placebo comparison). At day 57, 12% and 34% of patients in the 2.0- and 0.5-mg/kg groups had clinically significant human anti-human antibody levels. This was suggestive of a dose-dependent beneficial effect of the drug on clinical remission.134

In a double-blind, placebo controlled trial, 181 patients with active UC received iv 0.5 or 2 mg/kg MLN-02 or placebo at day 1 and 29. Both doses of MLN-02 achieved better clinical and endoscopic response in patients compared with placebo.135

Anti-ICAM-1 therapy

ICAM-1 seems to play a role in cell-mediated inflammation, specifically cell trafficking.

Alicaforsen (ISIS 2302) is an antisense to ICAM-1 (CD54) which was specifically designed to inhibit ICAM-1 expression. Theoretically, alicaforsen could be useful in the treatment of IBD patients.

Systemic treatment in CD patients revealed no significant results.

In UC patients, topical application in the form of enemas has demonstrated some effect in secondary outcomes, and initial studies in pouchitis are promising. The compound is well tolerated.136

Anti-IL-6R antibodies

Tocilizumab

Tocilizumab is a humanized anti-IL-6 receptor (IL-6R) monoclonal antibody which is produced using genetic engineering technology. Tocilizumab recognizes both the membrane-bound and the soluble form of IL-6R and specifically blocks IL-6 actions. As a consequence the drug is expected to be able to ameliorate inflammatory processes resulting from IL-6 overproduction.

The drug has been approved in the European Union for treatment of rheumatoid arthritis. It has also been studied for potential use in the treatment of CD.137

Immunostimulators

It has been suggested that some defects in the innate immune system may play an important role in the pathogenesis of CD. In the last 2 years a number of substances stimulating the innate immune system have been tested in patients with CD.

Recombinant human granulocyte-macrophage colony-stimulating factor (sargramostim)

Sargramostim is a recombinant human granulocyte-macrophage colony-stimulating factor (GM-CSF) that activates innate immunity.

In a randomized trial, 87 steroid-dependent CD patients received sargramostim and 42 placebo. Significantly more sargramostim-treated patients achieved CS-free remission (18.6% versus 4.9%; P = 0.03) and improvement in health-related quality of life. However, patients who received sargramostim experienced in a greater degree musculoskeletal pain, injection site reactions, and dyspnea compared with placebo.138 In another study the subcutaneous administration of sargramostim at a dose of 6 μg/kg/day improved the CDAI score although only a minority of patients experienced clinical remission or clinical response.139 Finally, 124 patients with moderate/severe CD received 6 μg/kg of sargramostim sc or placebo daily for 56 days. Although the primary endpoint (reduction of the CDAI of at least 70 points at day 57) was not achieved, all secondary end-points were achieved.140 The drug must be further investigated.

Recombinant human granulocyte-colony stimulating factor (filgrastin)

Filgrastin, a recombinant human granulocyte-colony stimulating factor (G-CSF), has also been tested in CD. Twenty patients with active CD received daily 300 μγ rhu G-CSF sc in a 12-week open-label study. At week 12, 25% of patients achieved clinical remission while 55% and 35% achieved 70 and 100 point reductions in the CDAI score, respectively. There were no significant side-effects except mild bone pain.141

Growth factors

Human growth factors are signaling molecules that lead to ligand-specific signal transduction. Their downstream effects are associated with several cellular functions including epithelial healing in response to injury. Impaired epithelial repair represents an important pathophysiological event in IBD.

Specific growth factor deficiencies have been noted in patients with IBD. The mode of action of these factors seems to be related to reduction of bowel permeability and enhancement of mucosal healing.

Several growth factors including growth hormone, epidermal growth factor, keratinocyte growth factor, teduglutide, and GM-CSF/G-CSF have emerged as potential tools for the modulation of intestinal inflammation and repair. Despite promising results of initial studies, the evidence to justify treatment of patients is inadequate. Specifically, keratinocyte growth factor-2 and epidermal growth factor did not show efficacy in phase II trials concerning patients with either CD or UC.142

T-cell directed therapies

In patients with IBD, T-cell-mediated immune responses directed against normal components of the gut flora play a significant role in amplifying and sustaining the mucosal inflammation by producing huge amounts of cytokines. Strategies aimed at interfering with T-cell accumulation and/or function in the gut have been employed with clinical success in patients with IBD.143

Therapeutic targets include modulators of CD80 or CD86-CD28 co-stimulatory signal (abatacept), CD2 receptors on T-cells (alefacept), CD11a, subunit of leukocyte function-associated antigen 1 (efalizumab), vitronectin receptor, and CD20 antigen on pre-B, immature, and mature B cells (rituximab).144

Inhibitors of Th1 polarization

It has been shown that in patients with CD the production of IL-12 and IL-18 results in Th1 polarized immune response and increased secretion of pro-inflammatory cytokines. It is logical therefore to test the efficacy of agents aiming to block the production of IL-12 and IFN-γ in patients with CD.

Anti-INF-γ antibodies (fontolizumab)

Fontolizumab is a humanized anti-IFN-γ antibody that has been tested recently in patients with CD. The administration of this antibody is based on the knowledge that elevated gut mucosal levels of INF-γ are associated with disease symptoms.

A total of 201 patients with active CD was randomized to receive an initial iv dose of 1.0 or 4.0 mg/kg fontolizumab or placebo, followed by up to three sc doses of 0.1 or 1.0 mg/kg fontolizumab or placebo every 4 weeks. On day 29 response rates were similar in all treatment groups (31% to 38%). Subsequently a greater proportion of patients in the 1.0 mg/kg iv/1.0 mg/kg sc fontolizumab group achieved clinical response and greater improvement in the CDAI score compared with patients who received placebo. All fontolizumab groups had significant improvement in CRP levels. The frequency of adverse events was similar in all groups.145 Although a strong clinical response to fontolizumab was not observed, significant decrease in CRP levels suggest a biological effect.

Anti IL-12 antibodies (ustekinumab)

Ustekinumab is a monoclonal antibody against the p40 subunit of IL-12/23, 2 important cytokines implicated in CD pathophysiology.

In a double-blind, cross-over trial 104 patients with moderate-to-severe CD were given sc placebo at weeks 0 to 3, then ustekinumab at weeks 8 to 11; sc ustekinumab at weeks 0 to 3, then placebo at weeks 8–11; iv placebo at week 0, then ustekinumab at week 8; or iv ustekinumab at week 0, then placebo at week 8. Clinical response rates for the combined groups given ustekinumab and placebo were 53% and 30% (P = 0.02), respectively at weeks 4 and 6, and 49% and 40% (P = 0.34), respectively, at week 8. In a subgroup of 49 patients who were previously given IFX, clinical response to ustekinumab was significantly greater than the group given placebo through week 8. Furthermore, in an open-label trial on the effects of 4 weekly sc injections or one iv infusion of ustekinumab in 27 patients who were non-responders to IFX, the clinical responses at week 8 to sc and iv ustekinumab were 43% and 54%, respectively.146 In a subsequent analysis of the alterations of levels of serum CRP the authors stressed that the potential benefit of ustekinumab in CD was further supported by serum CRP reduction. It seems that increased systemic inflammation as manifested by higher baseline CRP values leads to larger treatment effects with ustekinumab, especially in patients previously treated with IFX.147

Apilimod

Apilimod mesylate (formerly STA-5326) is an orally administered IL-12 and IL-23 inhibitor.

A phase II study evaluated the efficacy of the drug in treating 220 adult patients with CD. Patients received placebo or apilimod mesylate 50 or 100 mg daily. A clinical response was experienced by 24.7% in the 50-mg daily group and by 25.7% in the 100-mg group, compared with 28.8% in the placebo group on day 29 (no significant differences). Apilimod did not demonstrate efficacy over placebo in patients with active CD.148

Inhibitors of T-cell proliferation

Selective blockade of lymphocyte-vascular endothelium interactions in the gastrointestinal tract seems to be a promising therapeutic strategy for IBD. A number of monoclonal antibodies have been developed and tested in patients with UC during recent years.

Visilizumab

Visilizumab is a humanized IgG2 monoclonal anti-CD3 antibody. In an open-label phase I study performed on patients with severe UC, 32 subjects who had not previously responded to a 5-day regime with iv CSs received visilizumab at a dose of 10 or 15 μg/kg, on two consecutive days. On day 30, 84% of patients demonstrated a clinical response, 41% achieved clinical remission, and 44% achieved endoscopic remission; 45% of patients did not require salvage therapies or colectomy during the first year postdose. Mild to moderate symptoms of cytokine release occurred in 100% and 83% of patients in the 15- and 10-μg/kg dose groups, respectively. All patients exhibited a decrease in circulating CD4(+) T-cell, which returned to baseline values by day 30 in 26 of 30 evaluable patients (86%). There were no serious infections. Visilizumab had an acceptable safety profile at the 10-μg/kg dose level and may be clinically beneficial in patients with severe CS-refractory UC.149

In another study 104 patients were treated with visilizumab. The drug induced both symptomatic response and clinical response. Results with 5 μg/kg/day were similar to those observed with higher doses. However, all patients experienced adverse events.150

Basiliximab

Basiliximab is a chimeric IgG1 monoclonal antibody that targets CD25. This action is not associated with the release of cytokines because basiliximab has no cytoplasmic tail.

In an open-label, uncontrolled trial 20 patients with severe and moderate steroid-resistant UC were given a single dose of 40 mg basiliximab plus standard steroid therapy. Within 8 weeks, 10 of 20 (50%) patients achieved clinical remission. At 24 weeks, 13 of 20 (65%) patients were in clinical remission. Five patients required colectomy. Treatment was well tolerated.151

Basiliximab appears to promote prolonged remission after a single treatment, and shows particular promise in moderate steroid-resistant UC.

Daclizumab

Daclizumab is a humanized IgG1 monoclonal antibody targeting CD25. In a double blind, placebo-controlled trial, 159 patients with active UC were randomized to receive induction therapy with daclizumab 1 mg/kg iv at weeks 0 and 4, or 2 mg/kg iv at weeks 0, 2, 4, and 6, or placebo. Two percent of patients receiving daclizumab 1 mg/kg (P = 0.11 versus placebo) and 7% of patients receiving 2 mg/kg (P = 0.73) were in remission at week 8, compared with 10% of those who received placebo. Response occurred at week 8 in 25% of patients receiving daclizumab 1 mg/kg (P = 0.04) and in 33% of patients receiving 2 mg/kg (P = 0.30) versus 44% of those receiving placebo. Patients with moderate UC who are treated with daclizumab are not more likely to be in remission or response at 8 weeks than patients treated with placebo.152

Anti-inflammatory cytokines

Recombinant human IL-10

In a recent meta-analysis aim to assess the efficacy and tolerability of IL-10 for induction of remission in patients with active CD, no significant differences were found between the drug and placebo in complete remission or clinical remission. Patients treated with IL-10 were more likely to withdraw from the studies due to adverse events. Therefore, IL-10 does not appear to provide any benefit for the treatment of active CD.153

Immunomodulators

IFN-β1a has been shown to downregulate the expression of IL-12, a cytokine that is thought to be involved in mucosal degeneration in CD.

In a multicenter, double-blind, placebo-controlled, phase II, dose-finding study, patients with steroid-induced clinical remissions of CD were randomized 1:1:1:1 to sc IFN-β1a: 66 μg three times weekly, 44 μg three times weekly, 44 μg twice weekly, or placebo three times weekly with steroid tapering. The study was terminated after a planned interim analysis at 26 weeks because there was no difference in efficacy between patients with CD receiving IFN-β1a or placebo.154

During the past decade a better understanding of the underlying pathogenesis of IBD along with great advances in biotechnology has resulted in the introduction of many biologic therapies, other than anti-TNF-α. We now can target many other proteins or receptors including the protein subunit p40, as well as antibodies that are able to block adhesion molecules in the areas of inflammation.

Among the new biologic agents, natalizumab produced quite satisfactory results in patients with CD and is currently in regular use in the United States. However, attention must be given to the possible side-effects of the drug. A good suggestion is to use natalizumab as an alternative therapeutic option after failure or intolerance of other anti-TNF-α agents.

Results from trials on the use of antibodies against IL-12 and IL-6R in patients with CD produced relatively satisfactory results, although studies including large numbers of patients are needed. In patients with CS-refractory UC, basiliximab could be an effective agent.

We must stress the fact that so far no studies have compared head-to-head anti-TNF antibodies with other biological agents belonging to other classes such as natalizumab.

Despite promising results of the initial studies on the use of growth factors, the evidence to justify treatment of patients with CD is inadequate. Because the administration of anti-inflammatory cytokines or immunomodulators produced negative results their use at present is not justified.

Ustekinumab, the monoclonal antibody against the p40 subunit of IL-12/23, seems to be promising in patients with active CD, especially in those with high baseline CRP values.

Because the data on the efficacy and short- and long-term safety of these new biologic agents are limited, their use in IBD patients remains to be justified.

Microbes and microbial products

Helminths

In Western countries modern hygienic practices prevent exposure to parasitic worms. Epidemiologic studies suggest that people harboring infection from helminths are affected by immune-mediated disease to a lesser degree. Consequently, people living in less developed countries are probably protected from IBD development. This epidemiological assumption is further supported by experimental data showing that mice colonized with helminths are protected from the development of experimental colitis.155 The ‘IBD hygiene hypothesis’ states that raising children in extremely hygienic environments impairs immune development, which predisposes them to immunological diseases such as IBD later in life.156 Helminths stimulate immune regulatory circuitry by interacting with host innate and adoptive immunity, thus reducing aberrant inflammation.

It seems therefore that exposure to helminths may help prevent or even ameliorate IBD. The most important studies on the safety and possible efficacy of the intestinal helminth Trichuris suis in the treatment of patients with active CD are discussed below.

Efficacy of helminths in Crohn’s disease

Twenty-nine patients with active CD ingested 2500 live T. suis ova every 3 weeks for 24 weeks. At week 24, 79.3% responded and 72.4% remitted. Analysis at week 12 yielded similar results.157 There were no adverse events. Helminth therapy may offer a unique, safe, and efficacious alternative for CD management.

Efficacy of helminths in ulcerative colitis

In animal models, helminths prevent or improve colitis by inducing regulatory T cells and modulatory cytokines.

In a randomized, double blind, placebo-controlled trial aiming to determine the efficacy and safety of the helminth T. suis in UC, Summers et al assigned 54 patients with active UC, to receive 2500 T. suis ova or placebo orally at 2-week intervals for 12 weeks. After 12 weeks, improvement occurred in 43.3% of patients with ova treatment compared with 16.7% given placebo (P = 0.04). Treatment induced no side-effects.158

Cholera toxin B subunit

Cholera toxin B subunit has been shown to ameliorate experimentally induced colitis in mice.

In a recent study aim to evaluate the safety and efficacy of recombinant cholera toxin B subunit in CD patients, an oral solution of 5 mg recombinant cholera toxin B subunit was administered to 15 patients with CD three times per week for 2 weeks. A significant decrease in CDAI score was observed. Response rates were 42% in the per-protocol analysis; 40% were in remission at 4 weeks and 30% at 8 weeks post-treatment.159 No significant side-effects were noted. Treatment with recombinant cholera toxin B subunit seems to be safe, leading to a 40% treatment response.

The results of these studies suggest that microbes and microbial products (especially ova therapy) could be a safe and effective therapy in patients with both active CD and active UC. However, we suggest that further studies including a large number of patients with different types of IBD are needed before considering helminth treatment as an alternative therapy for patients with IBD.

Omega-3 free fatty acids

Because of their anti-inflammatory action, omega-3 poly-unsaturated fatty acids (PUFA) may be beneficial in IBD. A large body of evidence supports a protective effect of omega-3 PUFA in experimental animals and ex vivo models of CD and UC. Although fish oil supplementation in patients with IBD results in omega-3 PUFA incorporation into gut mucosal tissue and modification of inflammatory mediator profiles, the evidence of clinical benefits of omega-3 PUFA is weak.160

A study aim to determine whether the oral administration of omega-3 free fatty acids is more effective than placebo for prevention of relapse of CD showed that 4 g/day of omega-3 free fatty acids for up to 58 weeks was not more effective in preventing relapse of CD than placebo.161

Leukocytapheresis

In patients with active IBD a large number of activated myeloid leucocytes infiltrate the colonic mucosa. Myeloid leucocytes produce large amounts of TNF-α. It is possible, therefore, that selective granulocyte/monocyte adsorption could promote remission in active UC. The mode of action of granulocyte/monocyte adsorption appears to be more than adsorption of excess neutrophils and TNF-producing monocytes. Adsorbed granulocyte/monocytes release IL-1 receptor antagonist, hepatocyte growth factor, and soluble TNF receptors, which have anti-inflammatory properties.162

It is generally accepted that leukocytapheresis treatment of patients refractory to conventional UC therapy could produce very satisfactory results.163

More intensive leukocytapheresis seems to be more efficacious than weekly treatment. It can significantly reduce patient morbidity time without increasing the incidence of side-effects.164

Unfractioned and low-molecular-weight heparin

According to a recent meta-analysis on the use of unfractionated heparin and low-molecular-weight heparins (LMWH) in patients with active UC, sc LMWH showed no benefit over placebo. However, high doses of LMWH administered via an extended colon-release tablet demonstrated benefit over placebo for clinical remission and clinical and endoscopic improvement. There is evidence to suggest that LMWH may be effective for the treatment of active UC, a benefit that needs to be confirmed by randomized controlled studies. There is no evidence, however, to support the use of unfractionated heparin for the treatment of active UC. When deciding to administer LMWH in patients with active UC the benefit must be balanced against an increased risk of rectal bleeding.165

Other substances

Anti-oxidants

Oxidative stress plays a significant role in the pathogenesis of IBD. In a preliminary study it was reported that rectal d-alpha tocopherol enema (8000 U/day) may represent a novel therapy for mild and moderately active UC, probably owing to the anti-inflammatory and anti-oxidative properties of vitamin E.166

Statins

Experimental and clinical data have suggested that statins can downregulate both acute and chronic inflammatory processes. In a study including a small number of patients, atorvastatin therapy reduced inflammation in patients with CD, thus encouraging further investigation in IBD patients.167

Rosiglitazone

Thiazolidinedione ligands for PPAR-γ receptors have been proposed as novel therapies for UC.

In a randomized, double-blind, placebo-controlled clinical trial the efficacy of rosiglitazone 4 mg orally twice daily versus placebo twice daily for 12 weeks was studied in 105 patients with mild-to-moderate UC. Rosiglitazone was shown to be efficacious.168 In another study combined treatment with rosiglitazone and mesalazine achieved better results than mesalazine alone.

Rosiglitazone can alleviate colonic inflammation, which we hope will become a novel agent for UC treatment.169

Drugs used in the treatment of pouchitis

Pouchitis is the major long-term complication after ileal-pouch-anal anastomosis for UC. More than 15% of operated patients can develop chronic pouchitis, either treatment-responsive or treatment-refractory. During recent years the treatment of refractory pouchitis has progressed significantly.

In a Cochrane systematic review on the efficacy of medical therapies for pouchitis it was found that ciprofloxacin was more effective in inducing remission than metronidazole. Lactobacillus GG were more effective than placebo, while budesonide enemas and metronidazole were similarly effective in inducing remission of the active disease. Other substances were also tried in patients with pouchitis (including glutamine and butyrate suppositories) but unfortunately produced no statistically significant results.

Bismuth carbomer foam enemas did not show efficacy, while VSL#3 was more effective than placebo in maintaining remission of chronic pouchitis. For the prevention of pouchitis, allopurinol and inulin also seem to be of benefit.170

Budesonide

In an open-label study 20 patients with active pouchitis not responding after 1 month of antibiotic treatment were treated with budesonide controlled ileal release 9 mg/day for 8 weeks; 75% achieved remission. Budesonide seems to be an important alternative treatment in this kind of patient.171

Rifaximin

In a placebo-controlled pilot study aiming to evaluate the efficacy and safety of rifaximin 400 mg or placebo three times daily for 4 weeks in patients with active pouchitis, clinical remission occurred more frequently in patients treated with rifaximin but the difference was not significant in this pilot study. Further studies are required in order to determine if rifaximin is effective in active pouchitis.172

Conclusion

During the last decade we have seen the development of a large number of biological agents against TNF-α, as well as many biochemical substances and molecules specifically for the medical treatment of patients with inflammatory bowel disease. This revolution was a consequence of significant advances in biotechnology along with an increased knowledge of the underlying pathophysiologic mechanisms of the disease. Among others, natalizumab has shown quite good results in CD patients while basiliximab has shown efficacy in steroid-refractory UC. Leukocytapheresis has shown satisfactory results in steroid-refractory patients with UC. Unfractionated heparin and LMWH have been studied in patients with active UC with encouraging results. Microbes and microbial products including eggs of helminths seem to reduce disease activity in patients with UC or CD.

Helminths could act as adjuvants for induction of T regulatory cells which inhibit the maturation of CD4 T cells to Th1 and Th2 effector cells, and reduce the occurrence of Th1-mediated diseases (such as CD) and Th2-mediated diseases (such as UC). Chronic helminth infestation provokes a state of chronic immune activation with anergy. Administration of ova of T. suis has given encouraging results in the treatment of CD and UC with a good safety record, but long-term trials are needed because of the potentially harmful effects of helminths on immunity.

Omega-3 fatty acids, antioxidants, statins and many other molecules are under investigation.

However, as stressed earlier, the true value of these new agents must not be overestimated, as their therapeutic success is limited and the costs per induced remission are quite high.

It is hoped that this enormous effort to discover new ways of treating IBD will make us more optimistic for the future of our patients suffering from this enigmatic disease.