Psoriasis, anti-tumor necrosis factor therapy, and tuberculosis: report of three challenging cases and literature review.

INTRODUCTION: The era of biologic therapies has provided new options for the treatment of chronic plaque psoriasis. However, safety concerns have led to intensive screening and monitoring of patients receiving anti-tumor necrosis factor alpha (anti-TNF-alpha) agents.
METHODS: The authors describe the cases of three patients with moderate to severe psoriasis treated with anti-TNF agents, with challenging diagnostic and treatment aspects regarding tuberculosis (TB) infection, a serious adverse event associated with this type of treatment. The cases are discussed in the context of a comprehensive literature review describing the risk of TB associated with the use of TNF inhibitors. A critical review of the clinical trials that have tested the safety of these agents is also presented.
RESULTS: One patient, who tested negatively for latent TB infection (LTBI) during screening, developed active TB under adalimumab therapy. For two other patients the diagnosis and management of LTBI in relation to anti-TNF therapy represented a challenge. Although clinical trials involving the use of anti-TNF therapy for psoriasis haven't demonstrated a high TB incidence, active TB is continuously reported in association with this treatment.
CONCLUSIONS: Findings from clinical practice and the scientific literature indicate that anti-TNF therapies are associated with an increased risk of TB, and close monitoring of patients is needed.

Introduction

Psoriasis is a chronic inflammatory systemic disease predominantly affecting the skin and joints. The prevalence ranges between 0.9% (United States) and 8.5% (Norway) [1]. Skin lesions are the major manifestation of the disease. They are described as scaling and erythematous plaques that may be pruritic or painful and cause significant quality of life issues [2].

The new era of biologic therapies offers outstanding options for the treatment of chronic plaque psoriasis, and these agents have proved to be remarkable in improving patient quality of life compared with classical antipsoriatic treatments. However, despite the high efficacy, there have always been concerns regarding the safety of these agents as all anti-tumor necrosis factor alpha (anti-TNF-alpha) agents have been associated with activation of latent tuberculosis infection (LTBI) in a relatively short period of time [3]. According to World Health Organization (WHO), the global incidence of tuberculosis (TB) is estimated to 125 cases per 100,000 population [4]. The progression or reactivation of TB should be expected and such concerns have led to intensive screening and monitoring of patients receiving anti-TNF therapies [5]. Current screening includes medical history, chest X-ray, and tests for evaluating the immunologic response to the presence of Mycobacterium tuberculosis, such as the tuberculin skin test (TST) and interferon gamma release assays (IGRAs) [6]. Current guidelines recommend TST as the main screening tool for LTBI in patients with psoriasis before initiation of anti-TNF therapy, but there is a lack of consensus on the interpretation of TST in this group of patients [7-9]. The European S3 guidelines recommend the use of either TST or IGRAs or both for LTBI detection [10]. However, as TST may produce false-positive results, the newest recommendations suggest the use of IGRAs [11].

Despite the screening programs for LTBI identification prior to anti-TNF therapy, the risk of developing active TB is still present. We report a patient with psoriasis who had a negative TST during screening and later developed active TB under adalimumab therapy. We also report two patients with challenging aspects regarding the diagnosis and management of LTBI in relation to anti-TNF therapy. Additional evidence from a review of the literature is also discussed.

Case Studies

Patient characteristics, TB status, and treatment received for all three case studies are summarized in Table 1.

Table 1

Patient characteristics and tuberculosis status of three cases studies

	Case 1	Case 2	Case 3
Age (years)	57	53	64
Sex	Male	Female	Female
PASI score before therapy	36	28	31
Duration of psoriasis (years)	18	9	21
Psoriatic arthritis	No	Yes	Yes
Other comorbidities	Hypertension	Hypertension	Type 2 diabetes, obesity hypertension, asthma, atopy
Systemic medications prior to anti-TNF therapy	Methotrexate	Methotrexate, leflunomide, sulfasalazine	Methotrexate, PUVA-therapy
Type of biologic therapy	Adalimumab	Infliximab, adalimumab	Infliximab, adalimumab
Duration of biologic treatment (months)	18	30	28 (4 months infliximab, 24 months adalimumab)
TB screening prior to biologic therapy
Chest X-ray	Negative	Negative	Calcified fibronodule
TST value (mm)	3	24	15
QFT-G	Not performed	Positive	Positive
TB tests during biologic therapy
Chest X-ray	Bilateral infiltrates	Fibronodular infiltrates	Calcified fibronodule
TST value (mm)	17	35	17
QFF-G	Positive	Positive	Positive
Chemoprophylaxis	No	Isoniazid, 9 months	Isoniazid, 2 months intolerance
Diagnosis	Active pulmonary TB	LTBI	LTBI

LTBI latent tuberculosis infection, PASI Psoriasis Area and Severity Index, PUVA psoralen combined with ultraviolet A, QFT-G QuantiFeron®-TB Gold, TB tuberculosis, anti-TNF anti-tumor necrosis factor

Case 1

A 57-year-old man presented with a 18-year history of severe chronic plaque psoriasis. The patient was hypertensive. He was previously treated with systemic methotrexate and topical antipsoriatic therapies. He did not report any known contact with a case of active TB.

Due to the poor response to classical treatments for psoriasis, adalimumab was recommended according to current guidelines [2]. All screening tests were within normal ranges, including a negative TST (3 mm induration) and chest X-ray. Therefore, adalimumab therapy was initiated without antituberculous chemoprophylaxis. The patient showed a good and stable response; the Psoriasis Area and Severity Index (PASI) decreased from 36 to 9 in 12 weeks, and all lesions were cleared after 6 months of treatment.

After 18 months of biologic therapy, the patient complained of a mild but persistent cough and loss of appetite. A subsequent TST was positive (17 mm). QuantiFeron®-TB Gold (QFT-G) test (Cellestis Inc., Valencia, CA, USA) was also positive. Chest X-ray and computed tomography (CT) both showed bilateral pulmonary infiltrates. Routine laboratory examinations, including complete blood count and biochemical profile, were within normal limits. The patient was referred to a pulmonologist who confirmed active pulmonary TB with positive microbiology. The patient discontinued adalimumab and tuberculostatic treatment was prescribed. After a 6-month course of a multidrug anti-TB regimen, the pulmonary lesions were completely cleared but the psoriasis progressively worsened. With the patient’s consent and the pneumologist’s approval, adalimumab was resumed with close follow-up.

After 6 months of follow-up, there was a marked improvement in the patient’s psoriasis and no report of any other side effects. Close monitoring of the patient will continue in order to rule out TB recurrence.

Case 2

A 53-year-old woman presented with a 9-year history of psoriasis vulgaris and psoriatic arthritis. She was previously treated with systemic methotrexate, leflunomide, sulfasalazine, and topical antipsoriatic therapies. She did not report any contact with a case of active TB.

The patient was screened before administration of biologic therapy. The patient’s TST value was 24 mm. Chest X-ray was negative. Clinical examination and routine laboratory tests were normal. Chemoprophylaxis with isoniazid (300 mg/day, 9 months) was prescribed, which was initiated 1 month before anti-TNF therapy. Subsequent treatment with infliximab was associated with a good response and complete clearing of skin lesions. Annual TST testing remained high in two repeated determinations (25, respectively 30 mm). No side effects were noted in the first 2 years of treatment.

After 30 months of biologic therapy, the TST was 35 mm, QFT-G was also positive, and a chest x-ray showed two pulmonary nodular lesions. CT showed two fibronodular infiltrates in the inferior lobe of left lung and middle lobe of the right lung. Routine laboratory tests were within normal limits. The patient was asymptomatic, but was referred to a pneumologist who, based on clinical suspicion, recommended interruption of anti-TNF therapy and initiation of a tuberculostatic regimen. However, the sputum specimens were negative for M. tuberculosis by smear and culture, and active TB was finally infirmed. The patient was diagnosed with LTBI, resuming biologic therapy with another biologic agent: etanercept. The patient developed a persistent injection-site reaction after four doses of etanercept, a side effect that led to cessation of this anti-TNF treatment and initiation of adalimumab as an alternative treatment. The patient’s condition is currently stable, with a continued response to adalimumab and no side effects after 6 months of follow-up. Close monitoring will continue in order to rule out reactivation of LTBI.

Case 3

A 64-year-old woman presented with a 21-year history of psoriasis. She suffered from psoriatic arthritis, type 2 diabetes mellitus, asthma, hypertension, atopy, and obesity. The patient reported allergic reactions to various medications, including penicillin, mometasone furoate, and aspirin. She had previously received systemic methotrexate and psoralen combined with ultraviolet A (PUVA) therapy and did not report any known contact with a case of active TB.

Prior to initiation of anti-TNF treatment with infliximab, she had undergone a TST with an induration of 15 mm and a positive QFT-G assay. Chest X-ray showed a calcified left apical fibronodule. Physical examination did not reveal any pathological findings. Routine laboratory tests were within normal range. The patient was diagnosed with LTBI and chemoprophylaxis with isoniazid 300 mg/day was prescribed. After 2 months of isoniazid, she developed erythema multiforme and treatment was stopped. An attempt was made to reintroduce the chemoprophylactic treatment but the skin lesions reappeared.

Due to the severity of her condition (severe psoriasis with a PASI score of 31 and psoriatic arthritis), she continued infliximab therapy with close pneumology follow-up. After the fourth infusion, she developed an anaphylaxis-like reaction to infliximab. The drug was discontinued and the patient was switched to adalimumab. The patient was treated successfully with adalimumab for 2 years without side effects. Monitoring will continue in order to rule out active TB.

Discussion

The advent of anti-TNF agents has revolutionized the therapeutic approach to psoriasis and other inflammatory disorders. However, as these therapies have become widely used in clinical practice, TB is increasingly recorded. The authors presented three cases of patients with challenging aspects regarding the risk of TB related to anti-TNF therapy. The first patient, excluding his psoriasis, was an otherwise healthy individual with no predisposing factors for TB. A TST response of 3 mm during the screening was considered negative. This suggests that even healthy individuals with no predisposing factors or evidence of LTBI should be cautiously monitored. The second patient started a multidrug anti-TB regimen, but the diagnosis of active TB was finally infirmed. In contrast, the third patient was diagnosed with LTBI and was treated successfully with biologic therapy for more than 2 years, despite a short course of a chemoprophylactic regimen with isoniazid.

TNF-alpha is a pro-inflammatory cytokine that stimulates the acute phase reaction. It has a broad spectrum of biologic effects: it stimulates inflammatory cytokines (interleukin [IL]-1beta, IL-6, IL-8, granulocyte–macrophage colony-stimulating factor [GM-CSF]) and chemokines (monocyte chemotactic protein-1 [MCP-1], Macrophage inflammatory protein [MIP]-1alpha, MIP-2, RANTES [regulated and normal T cell expressed and secreted]) [12], activates endothelial adhesion molecules (vascular cell adhesion molecule 1 [VCAM-1], intercellular Adhesion Molecule 1 [ICAM-1], E-selectin), induces apoptosis, and inhibits tumorigenesis and viral replication. TNF-alpha is important in the protection against M. tuberculosis through its role in granuloma formation. It recruits macrophages and lymphocytes, and is required for the maintenance of the granulomatous structure [13, 14].

The cytokines released by T cells play a critical role in TB pathogenesis through macrophage activation and granuloma formation. T-helper 1 (Th1) lymphocytes release interferon-gamma (IFN-γ) and TNF-alpha. These cytokines are involved in the transformation of macrophages into specialized histiocytic cells with bactericidal and bacteriostatic functions. Activated macrophages, under T-lymphocyte influence, organize and form the tuberculoid granulomas. In contrast, TNF-blockade is associated with granuloma lysis [9, 15].

Many randomized, controlled studies have evaluated the safety of etanercept, infliximab, and adalimumab [16, 17], the majority of which have been conducted in patients with rheumatologic conditions or Crohn’s disease. However, according to the Food and Drug Administration (FDA) Adverse Event Reporting System (AERS), only a single case of TB occurred during initial clinical trials of infliximab [18] and none of the patients treated with etanercept and adalimumab developed TB during the initial studies [9]. Despite these results, TB has been continuously reported in association with biologic therapy [19-22].

Data from the British Society for Rheumatology Biologics Register (BSRBR), analyzing 10,712 patients with rheumatoid arthritis treated with anti-TNF agents, reported 39 cases of active TB. The risk for TB was as follows: 144 events/100,000 patient-years for adalimumab; 136/100,000 patient-years for infliximab; and 39/100,000 patient-years for etanercept, confirming that infliximab and adalimumab are associated with a three- to fourfold higher rate of TB compared with etanercept. The median time to TB diagnosis was 13.4 months for patients exposed to etanercept, 5.5 months for infliximab, and 18.5 months for patients exposed to adalimumab [20]. Other publications have indicated a lower risk of TB in patients treated with etanercept compared with infliximab or adalimumab [17, 22–27].

The safety data from patients with rheumatoid arthritis can only partially be generalized to patients with psoriasis vulgaris, as psoriasis is typically treated with monotherapy whereas rheumatoid arthritis is commonly based on treatment regimens consisting of systemic immunosuppressants and biologics, which can increase the risk of infection [28].

The present authors searched the MEDLINE database for randomized, placebo-controlled studies of the three currently used anti-TNF agents (infliximab, etanercept, and adalimumab) published between 2003 and 2012. Study participants were adult patients with moderate-to-severe psoriasis treated with anti-TNF agents for at least 12 weeks. Based on these criteria, 13 clinical trials [29-41] were identified that collectively included 3,657 adult patients with moderate-to-severe psoriasis who were treated with adalimumab, etanercept, or infliximab (Table 2). The total number of patients receiving the placebo was 1,709. The treatment duration ranged from 12 to 52 weeks. All trials compared anti-TNF agents with the placebo: three trials with adalimumab, six trials with etanercept, and four trials with infliximab. Three studies [29, 40, 41] reported active TB as an adverse event occurring during anti-TNF therapy: one patient was treated with adalimumab and five patients received infliximab. Active TB was not reported in the placebo group.

Table 2

Phase 3, randomized, placebo-controlled trials of infliximab, etanercept, and adalimumab

References	Anti-TNF	Duration (weeks)	Anti-TNF group no. of patients	Patients with active TB	Efficacy summary	Safety data	TB screening
Menter et al. [29]	Adalimumab 80 mg at W0, then 40 mg eow starting at W1	52	814	1	71% of adalimumab-treated patients achieved PASI75 after 16 weeks vs. 7% of placebo-treated patients	SAEs reported in 1.8% of cases, similar with control-group	Yes
Saurat et al. [30]	Adalimumab 80 mg at W0, then 40 mg eow starting at W1	16	108	0	79.6% of adalimumab-treated patients achieved PASI75 after 16 weeks vs. 18.9% in placebo-treated patients	SAEs reported in 1.9% of adalimumab-treated patients, similar with placebo-treated patients	Yes
Asahina et al. [31]	Adalimumab (i) 40 mg eow (ii) 80 mg at W0, then 40 mg eow starting at W2 (iii) 80 mg eow	24	123	0	PASI75 rates after 16 weeks of adalimumab were 57.9–62.8% to 81% vs. 4.3% in placebo-treated patients	4 of 123 adalimumab-treated patients experienced SAEs vs. 2 of 46 placebo-treated patients	Yes
Gottlieb et al. [32]	Etanercept 25 mg twice weekly	24	57	0	30% of etanercept-treated patients achieved PASI75 after 12 weeks vs. 2% of placebo-treated patients	2 of 57 etanercept-treated patients experienced SAEs vs. 2 of 55 placebo-treated patients	No
Leonardi et al. [33]	Etanercept (i) 25 mg weekly (ii) 25 mg twice weekly (iii) 50 mg twice weekly	24	486	0	PASI75 rates after 12 weeks of etanercept were 14–34–49% vs. 4% in placebo-treated patients	AEs of mild or moderate intensity, similar for etanercept-treated and placebo-treated patients	No
Papp et al. [34]	Etanercept (i) 25 mg twice weekly (ii) 50 mg twice weekly	24	390	0	PASI75 rates after 12 weeks of etanercept were 34–49% vs. 3% in placebo-treated patients	11 of 380 etanercept-treated patients experienced SAEs vs. 1 of 193 placebo-treated patients	No
Tyring et al. [35]	Etanercept 50 mg twice weekly	12	311	0	47% of etanercept-treated patients achieved PASI75 after 12 weeks vs. 5% of placebo-treated patients	1.9% of etanercept-treated patients experienced SAEs vs. 1% of placebo-treated patients	No
van de Kerkhof et al. [36]	Etanercept 50 mg weekly	24	96	0	37.5% of etanercept-treated patients achieved PASI75 after 12 weeks vs. 2.2% of placebo-treated patients	2.1% of etanercept-treated patients experienced SAEs vs. 6.5% of placebo-treated patients	Yes
Bagel et al. [37]	Etanercept 50 mg twice weekly for 12 weeks, then 50 mg once weekly	24	62	0	59% of etanercept-treated patients achieved PASI75 after 12 weeks vs. 5% of placebo-treated patients	3 SAEs were reported in etanercept-treated patients	Yes
Gottlieb et al. [38]	Infliximab (i) 3 mg/kg at W0, 2, 6 (ii) 5 mg/kg at W0, 2, 6	30	198	0	72–88% of infliximab-treated patients achieved PASI75 after 10 weeks vs. 6% of placebo-treated patient	12 SAEs were reported in infliximab-treated patients	Yes
Reich et al. [39]	Infliximab 5 mg/kg at W0, 2, 6, 14, 22	46	301	0	80	6	Yes
Menter et al. [40]	Infliximab (i) 3 mg/kg at W0, 2, 6 (ii) 5 mg/kg at W0, 2, 6	50	627	2	70.3–75.5% of infliximab-treated patients achieved PASI75 after 10 weeks vs. 1.9% of placebo-treated patients	12 of 627 infliximab-treated patients experienced SAEs vs. 5 of 207 placebo-treated patients	Yes
Yang et al. [41]	Infliximab	26	84	3	81% of infliximab-treated patients achieved PASI75 after 10 weeks vs. 2.2% of placebo-treated patients	4 of 84 infliximab-treated patients experienced SAEs vs. 1 of 45 placebo-treated patients	Yes

AEs adverse events, PASI75 75% improvement in the Psoriasis Area and Severity Index, SAEs serious adverse events, TB tuberculosis, anti-TNF anti-tumor necrosis factor, W week, eow every other week

Although clinical trials have demonstrated significant efficacy and a low number of TB cases in patients with psoriasis, questions remain about the long-term use of these agents. There are several limitations that make it difficult to assess the potential for anti-TNF therapy to promote TB infection. For example, the median time to TB diagnosis has been reported to range from 5.5 to 18.5 months [20], and these randomized, controlled studies extend to a limited period of time (3–13 months). From another point of view, the study of Yang et al. [41] highlights that TB is a major problem in endemic areas. Furthermore, clinical practice continues to provide details concerning the increasing numbers of patients with active TB, despite the screening methods for detecting LTBI [42-47].

TB often presents as extrapulmonary or disseminated disease in such patients and has been reported with the use of all of the anti-TNF agents [15, 18, 21, 48–51]. This form of presentation is explained by the underlying mechanism: the immunosuppression induced by anti-TNF therapy leads to reactivation of secondary foci and dissemination of M. tuberculosis [52]. The monoclonal antibodies form stable complexes with all forms of TNF-alpha, including TNF on the surface of macrophages and T cells, which induces T cell and macrophage apoptosis [53, 54]. In addition, biologic therapy inhibits the Th1 cell response, as well as the production of IFN, a cytokine with major roles in the immune defense against M. tuberculosis [55, 56]. Thus, these actions disturb granuloma integrity and increase the risk of secondary foci reactivation [52].

Active TB associated with biologic treatment is believed to be the result of LTBI reactivation in most cases. LTBI is defined as a complex clinical condition in which an infection with M. tuberculosis persists in a subclinical status with minimal replication. The bacilli are unable to cause clinical manifestations and cannot be identified in culture [57]. Identification of latent infection and chemoprophylaxis with isoniazid seems to decrease the risk of developing active disease [58]. Thus, an important prophylactic measure is the treatment of LTBI [59]. This approach reduces the reactivation risk by over 80% [60, 61]. However, de novo TB has also been reported [62, 63]. A short time to the onset of TB after the start of biologic treatment suggests LTBI reactivation as the new infections seem to occur at random during anti-TNF treatment. De novo TB is not influenced by anti-LTBI treatments. In these cases, new approaches are required, such as primary prevention [64].

Although current guidelines recommend screening prior to anti-TNF therapy, there are no standard indications and there is a lack of consensus on interpreting TST in patients with psoriasis. The consensus guidelines from the National Psoriasis Foundation, USA, state that an induration >5 mm is classified as positive in patients with immunosuppression, including patients who are receiving TNF antagonists [7]. The main disadvantage is that they do not provide specific guidelines on interpreting TST for patients about to start anti-TNF therapy [8]. Some authors consider that skin indurations of 5 mm or greater should be interpreted as a positive result for LTBI in any patient considered for TNF blockade [65]. This cut-off value is accepted by most guidelines, including the national guidelines, but it may overestimate LTBI in psoriatic patients, leading to unnecessary treatments. The present authors previously reported that patients with moderate-to-severe psoriasis had positive TST reactions more frequently (70.5%) than nondermatologic subjects (51%) [66]. Although the TST still represents a useful method, it is difficult to perform and read in psoriatic patients with extensive lesions, because these patients rarely present clinically unaffected skin for testing. Moreover, important immunologic mechanisms take place in even apparently healthy skin of psoriatic patients; the proinflammatory state can lead to an overreaction to antigenic triggers [67]. Another factor that may lead to false-positive results is the Koebner phenomenon (development of psoriatic lesions at the site of trauma), reported after intradermal injection of purified protein derivative (PPD) in psoriatic patients [68]. In contrast, psoriatic patients with negative TST results and positive QFT-G results have been reported [69-71]. The reversion of a positive TST result to a negative result may also occur [72]. Thus, to minimize the risk of false-negative results, some authors propose a booster dose 7–10 days after an initially negative TST [73]. Tubach et al. [3] reported 69 cases of TB in patients treated with anti-TNF agents, two-thirds of which occurred in patients with negative TST results at screening. However, the authors suggested that both reactivation of LTBI during the first year of treatment and new infections occurring during follow-up were responsible for the high incidence of TB reported in their study.

IGRAs are alternative tools for TB diagnosis. The principle of these methods is based on the detection of IFN-γ produced by the effectors memory T cells upon in vitro stimulation with the TB-specific antigens, early secretory antigen (ESAT) 6 and culture filtrate protein (CFP) 10. IFN can be measured using either ELISpot-based assay, represented by T-SPOT®.TB (Immunotech, Abingdon, UK), or an enzyme-linked immunosorbent assay (ELISA), represented by QFT-G and QFT-in-tube (QFT-IT; Cellestis, Victoria, Australia) [74]. Although QFT-G demonstrates high specificity for LTBI (96–99%), its sensitivity is still questionable (70–78%) [75]. In one study, LTBI treatment was avoided in 20% of patients with positive TST results but negative IGRA results [76].

The use of both methods in parallel can enhance both sensitivity and specificity. Furthermore, routine periodic retesting during therapy could allow for the detection of possible conversions. However, serial TST testing is not strictly recommended due to the boosting effect [60]. There is also evidence that the TST can boost subsequent IGRA results. The effect is evident after the first 3 days post-TST testing and potentially wanes after a few months [77]. Furthermore, the use of IGRAs during immunosuppressive treatment (including biologic therapy) is controversial, because the immunosuppression might decrease the production of IFN and interfere with the results [74].

Another inconvenience for both TST and IGRAs is the lack of discrimination between latent and active TB [60]. Positive TST/IGRAs tests at baseline often remain positive despite a successful anti-TB treatment. In these cases careful monitoring for clinical signs and symptoms of active TB is recommended [78].

According to the Tuberculosis Network European Trials Group (TBNET) consensus, the chemoprophylactic regimens recommended for LTBI include 6 or 9 months with isoniazid, 3 months of rifampicin plus isoniazid, or 4 months of rifampicin [79]. Another regimen used in the USA includes rifampicin and pyrazinamide for 2 months, although this regimen has been associated with a high number of side effects [80].

The diagnostic tools for active TB infection include clinical assessment, cultures for M. tuberculosis, staining for acid-fast bacilli, chest X-rays, and nucleic acid amplification assays [9]. Although culture is considered the reference standard, in clinical practice the diagnosis and treatment of TB are usually based on the presence of abnormal radiologic findings or clinical suspicion [20].

The recommendations for resuming biologic therapy in active TB patients are controversial. According to the American College of Rheumatology (ACR), anti-TNF therapy can be initiated or resumed after 1 month of chemoprophylaxis for LTBI and after completion of therapy for active disease [78]. The British Society for Rheumatology (BSR) accepts the continuation of biologic therapy during TB treatment if clinically indicated [81]. Hernandez et al. [82] reported 27 patients with active TB that resumed anti-TNF therapy before completing tuberculostatic treatment, without relapse during a 4-year follow-up.

In conclusion, anti-TNF agents are an established option for the treatment of psoriasis, but the safety profile should be carefully monitored. Even otherwise healthy patients with no predisposing factors for TB should be cautiously managed during biologic therapy. It is mandatory for the dermatologists who prescribe anti-TNF agents to carefully evaluate the patients to exclude concomitant TB and non-TB infections. Continuous vigilance, long-term follow-up, and systematic reporting of any suspected association between active TB and biologic therapy will improve the prevention and management of this complication.