The Therapeutic Role of Short-Chain Fatty Acids Mediated Very Low-Calorie Ketogenic Diet-Gut Microbiota Relationships in Paediatric Inflammatory Bowel Diseases.

The very low-calorie ketogenic diet (VLCKD) has been recognized as a promising dietary regimen for the treatment of several diseases. Short-chain fatty acids (SCFAs) produced by anaerobic bacterial fermentation of indigestible dietary fibre in the gut have potential value for their underlying epigenetic role in the treatment of obesity and asthma-related inflammation through mediating the relationships between VLCKD and the infant gut microbiota. However, it is still unclear how VLCKD might influence gut microbiota composition in children, and how SCFAs could play a role in the treatment of inflammatory bowel disease (IBD). To overcome this knowledge gap, this review aims to investigate the role of SCFAs as key epigenetic metabolites that mediate VLCKD-gut microbiota relationships in children, and their therapeutic potential in IBD.

1. Introduction

IBD is a distinct chronic, idiopathic, and relapsing disorder classified into two major conditions, including Crohn’s disease (CD) and ulcerative colitis (UC), which cause inflammation in the gastrointestinal tract (GIT). CD affects all parts of the GIT, but is localised most often to the colon and distal ileum, whereas UC affects the colon only [1]. IBD affects not only adults, but also children of all age groups, with higher rates of CD than UC and/or IBD-unclassified (IBDU) reported in most Western countries. In contrast, data from developing countries suggests higher rates of UC than CD [2]. When IBD is detected in children, overlapping histological, radiologic, and clinical features may pose a challenge differentiating between CD and UC [3]. A diagnosis of IBDU occurs when children have features on histological and clinical evaluations that are inconsistent with either CD or UC children [4]. However, it has been shown that IBDU children share similarities of molecular analysis of gene expression and serological features only with UC children two years after the diagnosis of IBDU [5]. Globally, the incidence of IBD in children under 19 years of age at diagnosis increased between 1985 and 2018 as follows: 0.1 to 13.9/100,000 for CD; 0.1 to 10.6/100,000 for UC; and 0.1 to 3.6/100,000 for IBDU [6]. Due to this increase, researchers have been exploring treatment options to manage paediatric IBD. The currently preferred treatments are largely focused on a group of biological agents that have been approved for use in the treatment of CD and UC/IBDU. The anti-tumour necrosis factor (TNF) agents, adalimumab (commercialised as Humira®) and infliximab (commercialised as Remicade®), have been shown to be effective in reducing moderate-to-severe complications of CD in children, and might be clinically beneficial against UC in children [7]. Vedolizumab (commercialized as Entyvio®), a humanised α4β7-integrin antagonist, was also demonstrated by a few retrospective studies to be effective in maintaining remission in children with CD and UC/IBD-U [8]. Recently, etrolizumab, a humanised anti-β7 antibody, has been demonstrated to have treatment efficacy in children diagnosed with moderate-to-severe CD and UC [9].

Although the aetiology of paediatric IBD is not well known, it is thought that key contributing factors, including genetics (e.g., loss of function variants in specific genes) [10] and the environment (e.g., dietary patterns, exposure to antibiotics, air pollution, appendectomy, enteric infections) [11], may lead to the development of disease, which exacerbates inflammatory immune responses. There is also growing interest in gut microbiota as another potential factor contributing to IBD pathogenesis. The colonization of the gut with diverse microbes is thought to occur during delivery and immediately after birth, and is influenced by multiple factors, including maternal gut microbiota, nutrition, antibiotic exposure, mode of feeding/delivery, and body mass index (BMI) [12]. Immune system development in early life may interact with gut microbiota composition, and the depletion of beneficial microbes may increase the risk of inflammatory diseases [12]. The gut microbiota has maintained a symbiotic relationship with its host through a range of functions, such as facilitating immune system development, protection from pathogenic bacteria, strengthening the integrity of the digestive tract, and production of beneficial metabolites such as SCFAs [13]. Butyrate, propionate, and acetate are the main fermentation-derived SCFA metabolites from indigestible complex carbohydrate (CHO) produced by gut microbes belonging to the phylum, Firmicutes, through a range of cross-feeding mechanisms/microbial metabolic pathways [14]. The metabolic cross-feeding of lactate, an intermediary metabolite formed by Bifidobacterium and lactic acid bacteria (LAB), can enhance the production of butyrate [15]. Although the gut microbiota composition of children with IBD differed from that of healthy children in several studies, it is consistently characterised by reduced abundances of SCFA-producing bacteria considered as ‘healthy microbiota’. The gut microbiota of children with CD and/or UC showed decreased genera belonging to the phyla, Actinobacteria (Bifidobacterium), Firmicutes (Lactobacillus, Blautia, Ruminococcus, Faecalibacterium prausnitzii, Roseburia), and Bacteroidetes (Bacteroides). However, the genera, Escherichia, Actinobacillus, Granulicatella, Enterococcus, and Streptococcus, were observed to have increased [16,17].

Diet has proven to be a major factor influencing gut microbiota composition, and, thus, is thought to be a significant environmental trigger in IBD. For example, consuming a high-fat diet and/or high-sugar diet could result in gut microbiota dysbiosis, characterised by reduced SCFA-producing bacteria, thereby dysregulating gut immune homeostasis and increasing susceptibility to gut inflammation, all of which contribute to IBD risk [18]. The results generated from intervention studies in adult IBD patients suggest that dietary fibre and prebiotics increase SCFA production and the abundance of bacteria they produced, thereby reducing gut inflammation and IBD risk [19]. It has been recently shown that higher intakes of prebiotics and other beneficial foods, including fruits, vegetables, honey, oats, legumes, omega 3 fatty acids, and lean animal protein, increase SCFA-producing bacterial taxa abundances and reduce levels of inflammatory cytokines (e.g., interleukins IL-6/IL-8 and TNF-α) in adult patients with CD and UC [20]. The CD exclusion diet combined with partial enteral nutrition or the exclusive enteral nutrition (EEN), provided in a liquid, low-saturated-fat/heme/taurine and high-protein polymeric formula, are found to be effective nutritional therapies in inducing remission in children with CD [21,22,23,24,25]. However, the introduction of EEN therapy was found to decrease SCFA levels (including butyrate) and the α-diversity of SCFA-producing bacteria, with a lower abundance of Bifidobacterium, Bacteroides, Ruminicoccus, F.prausnitzii, and Blautia [21,26,27,28], which are thought to be associated with reduced gut inflammation in CD. Thus, there is a need to explore food-based, diet-induced microbial changes to reduce gut inflammation in IBD. Treatment with the specific carbohydrate diet (SCD) that includes corn, wheat, food additives, and milk, or SCD with rice and oats, have been shown to increase the relative abundance of Blautia and F.prausnitzii in children with CD [29]. Adherence to the Mediterranean diet based on a high intake of fruits, vegetables, seafoods, olive oil, legumes, and nuts, has been associated with increased gut SCFA-producing bacterial diversity, with an increased abundance of F.prausnitzii in children [30], and has also demonstrated a significant decrease in inflammatory cytokines (IL-12, IL-13, IL-17, and TNF-α) in children with CD and UC [31].

There has been increased interest in the standard ketogenic diet (KD); namely, the very low-calorie ketogenic diet (VLCKD) as an effective restricted dietary pattern influencing SCFA-producing bacteria, thereby modifying inflammation-associated disease risk in early life [32,33]. There is little evidence to support the health benefits that the VLCKD has in paediatric IBD. Only one case report has revealed that Palaeolithic KD improves CD symptoms and progression in children [34]. It is hypothesized that the VLCKD influences SCFA-producing bacteria and reduces gut inflammation in IBD. However, the mechanism by which SCFAs could mediate VLCKD–gut microbiota relationships and the therapeutic implications for reducing IBD are largely unknown. Thus, this review highlights the potential role of SCFAs in the epigenetic mechanism underlying these effects.

2. Methods

A literature search of the PubMed/Medline database was carried out to identify in vitro/human studies published in English over the last 20 years using the following search keywords: children, IBD, intestinal epithelial cells (IECs), intestinal inflammation, inflammatory markers, VLCKD/KD, SCFA, KBs, gut microbiota, and epigenetic. Experimental studies, observational studies, randomised controlled trials (RCTs), and reviews were included for the purposes of this review. In vivo studies or studies of animal models were excluded from the review.

3. Epigenetics of Paediatric IBD

Epigenetics has revealed a potential mechanism that may explain how environmental triggers and genetic susceptibility interact in IBD [35]. Evidence from many studies suggests that epigenetic modification, in particular DNA methylation, which exists at cytosines in the cytosine–guanine (CpG) dinucleotide context, plays a key role in paediatric IBD phenotypes, as it is considered a key regulatory mechanism of gene expression in response to environmental cues, without modifying the primary nucleotide sequence [36,37]. However, the little evidence that exists examining histone methylation suggests that this modification takes place in the intestine of paediatric IBD. In CD children, genes exhibiting decreased histone H3-lysine 4 trimethylation (H3K4me3) signatures are found to be associated with the severity of inflammation in IECs [38]. Ileal IECs play a significant role in integrating commensal microbiota-derived cues to regulate immune homeostasis and gene expression. Genes characterized by increased H3K4me3 levels (e.g., DUOX2, NOS2) in IECs from CD children in response to commensal microbiota are enriched in several pathways, including the regulation of reactive oxygen species (ROS), G alpha signalling, digestive system development, and nitric oxide (NO) biosynthesis, suggesting that commensal microbiota may modify histone alterations that reflect intestinal inflammation in CD [38]. Large-scale, genome-wide studies have revealed significant mucosal DNA methylation changes in IBD-associated genes in children. For example, a systematic meta-analysis of 84 genetic studies identified specific genetic variants (rs11209026, rs7517847, rs12521868, rs26313667, rs1800629, rs2241880, rs2066847, rs2066844, and rs2066844) in differential DNA methylated genes (NOD2, IL23R, ATG16L1, IBD5, and TNF-α) known to cause CD and UC [36]. A study that assessed DNA methylation profiles of the colonic mucosa found that 182 CD and 3365 UC susceptible genes (including STAT3, SLPI, ITGB2, SAA1, IFITM1, and S100A9) were associated with differentially methylated regions (DMRs) [39]. Another study detected a number of UC-associated changes in DNA methylation at nine CpG sites located in the TRIM39-RPP21 gene [40]. In respect to the correlation between the colonic mucosal DNA methylation of paediatric IBD and microbiome changes, a study showed that SLC9A3, a gene with decreasing methylation UC-specific DMR, was associated with a reduced abundance of Bacteroides [41].

4. Role of Inflammatory Biomarkers in Paediatric IBD

Loss-of-function mutations in G-protein coupled receptors (GPCRs) may result in reduced ligand-binding affinity to many chemokines/cytokines, local mediators, and neurotransmitters during childhood development [42], which may lead to an increased risk of IBD. Naïve CD4+ T cells differ according to cytokine-producing T-helper (Th) subsets, including Th1 (interferon-gamma, IFN-γ, TNF-α), Th2 (IL-4, IL-5, IL-6, IL-13), and Th17 (IL-17) cells, which are implicated in the dysregulation of colonic mucosa in IBD patients [43,44]. Paediatric CD patients were shown to have a mixed Th1/Th2/Th17 cytokine profile, with increased serum levels of IL-1β, IFN-γ, IL-6, TNF-α, C-X-C motif chemokine ligand 10 (CXCL10), and IL-17A observed in both the ileum and colon [45,46]. Increased serum IL-4 and IL-6 levels were detected in the intestinal mucosa of paediatric UC patients, in which the GATA binding protein 3 (GATA3) and signal transducer and activator of transcription-4 (STAT4) signalling molecules were involved [47]. Compared with paediatric CD patients, significantly more mRNAs related to IL5, IL-13, IL-23, and IL17A cytokines were observed in the rectal mucosa of UC patients [48]. Serum levels of IL-6 were found to be higher in the ileum of paediatric CD patients than those of healthy children, whereas the serum levels of IL-22 and IL-17A were higher in UC patients than in CD patients [49]. Although Foxp3+Treg cells are found in higher density in the inflamed mucosa of paediatric IBD patients, they maintain immune homeostasis [49,50]. A higher density of Foxp3+ cells in the ileum of untreated paediatric CD patients compared with adult patients may be attributed to the disparate pattern of CD phenotypic expression [51]. In a previous in vitro experiment, serum levels of IL-17 and TNF-α were increased in the peripheral blood of paediatric patients with CD and UC. Patients displayed a decreased expression of Foxp3+, CD4+, and CD25+, and an increased percentage of Th17 cells. Myeloid dendritic cells (mDCs) and plasmacytoid DCs (pDCS) expressing CD200, a type I transmembrane glycoprotein, were found to be elevated, and significantly associated with Th17, but negatively associated with regulatory T cells (Tregs). On the contrary, the expression of the CD200 receptor, CD200R1, on mDCs was found to be reduced and negatively associated with Th17 [52]. The mRNA expression of pro-inflammatory cytokines IL-6 and IL-23 expressed at high levels in the colonic mucosa of paediatric patients with CD and UC is found to be associated with a higher frequency of CD4+ IL-17a+ and a lower frequency of CD4+Foxp3+Tregs [53]. An experimental study demonstrated that treatment with infliximab, a chimeric monoclonal antibody, does not inhibit the production of TNF-α, but also hampers expansion of FOXP3+ Tregs in the colonic mucosa of paediatric CD patients [54]. Another recent experimental study reported that paediatric patients with active CD and UC, though having a high expression of CTLA-4 in FOXP3+ Tregs in peripheral blood during pharmacological (aminosalicylates or azathioprine) therapy, showed a significant decrease of CD4+Foxp3+Tregs levels after therapy compared to the same patients and healthy children at disease onset [55].

In a human IBD model, which is characterised by increased histone deacetylases (HDACs), nuclear factor-κB (NF-κB), nuclear factor kappa-B kinase β (IKKβ), TNF-α, NOD2, and toll-like receptor (TLR) upregulation have been reported to occur in the inflamed IECs, resulting in high pro-inflammatory cytokine expression levels [56]. HDAC1 has been shown to be implicated in several diseases, in which it takes off the acetyl group from lysine residues of histone/non-histone proteins via acetyltransferases (HATs), which results in DNA inaccessibility, gene transcription repression, and chromatin compression [57]. The acetylation of histone H3 lysine 27, which is identified in regions with several risk loci for IBD [58], has been found to be downregulated in the inflamed mucosa of UC patients, resulting in high IL-6 mRNA levels [59]. HDAC1 induces an inflammatory response in the colon epithelium of UC patients by activating NF-κB, and reducing histone H3 acetylation and tight-junction protein, zonula occludens 1 (ZO-1), expression [60]. Loss-of-function NOD2 gene mutations enhance NF-κB activation, which, in turn, bind to the promoters of pro-inflammatory cytokines in paediatric CD patients [61]. This suggests that cytokines with pro-inflammatory effects could play a key role in the pathogenesis of paediatric IBD.

5. The VLCKD and Its Relationship to Gut Microbiota

The VLCKD is characterised by a high proportion of fat (70%), adequate protein (20%), and a low proportion of carbohydrates (CHO—10%, <50 g per day) [62]. This diet favours animal and/or plant-based sources of dietary fibre, protein, monounsaturated fatty acids (MUFA), polyunsaturated fatty acids (PUFA), and saturated fatty acids (SAT) (e.g., non-starchy vegetables, chicken, lamb, beef, eggs, cream, cheese, butter, olive oil) [63]. The VLCKD restricting CHO to either simple or complex CHO remains an active area for further investigations. Unlike sugars or simple starches, the dietary fibre, including both non-starch polysaccharide and resistant oligosaccharides-based foods, metabolised by the human colonic microbiota generate SCFAs [64,65,66,67,68,69], which play a significant role in regulating inflammatory immune responses [65,67]. Dietary fibre can also be considered as prebiotic-like galacto-oligosaccharides, which stimulates the growth of the gut microbiota and improves host health [66]. The daily fat intake should be high enough at around 70% of total calories to replace CHO intake and maintain ketosis. The daily protein intake should be kept moderate, at around 20% of total calories, because low-CHO–high-protein diets may not induce ketosis [62].

The VLCKD would be beneficial to achieve nutritional ketosis, a state known for its anti-inflammatory effects [32,33], which is characterized by increased blood levels of acetoacetate (ACA) and β-hydroxybutyrate (βOHB), the two main ketone bodies (KBs) produced in the liver and used as secondary energy sources when CHO stores are depleted [70]. βOHB has a structure and role in regulating gut homeostasis and gene expression through epigenetic modifications similar to butyrate, both of which may have therapeutic roles in treating inflammation-related diseases, such as obesity and asthma, in children [32,33]. During adherence to a VLCKD, hepatic glycogen stores are decreased, and FFAs are produced as an alternative energy source from adipocytes and regulated by insulin and glucagon. FFAs are then converted by β-oxidation to acetyl-coenzyme A (acetyl-CoA) in a process regulated by several enzymes that induce βOHB formation [71]. Butyrate serves synergistically with βOHB on inducing ketosis, in which it acts as a ligand to enhance receptors that the βOHB will also work on. Butyrate promotes fibroblast growth factor 21 (FGF21) in the liver, which enhances fatty acid β-oxidation for the production of βOHB, which can induce ketosis [72]. βOHB administration on human colonic microbiota models has been found to increase butyrogenesis and butyrate production [73].

The role of VLCKD in modulating/influencing the gut microbiota composition in paediatric IBD has been not investigated yet. The VLCKD has been shown to affect the gut microbiota of children by influencing the growth of SCFA-producing commensal microbes (e.g., Bifidobacterium, Lactobacillus, Bacteroides, Faecalibacterium, Clostridium, and Ruminococcus) in which epigenetic changes are involved [32,33]. The VLCKD exhibits an increase in circulating levels of βOHB, and induces epigenetic changes in the gut microbiota, suggesting that the anti-inflammatory effects of VLCKD in reducing IBD in children may be due to an increase in anti-inflammatory βOHB through epigenetic mechanisms by which SCFAs-producing bacteria could reduce the pro-inflammatory cytokines and chemokines in IBD children.

6. SCFAs as Epigenetic Modifiers in IBD

Diet–gene interactions play a key role in CD and UC pathogenesis, and this is why epigenetic modification of DNA/histone methylation could provide new insights outside the context of genetics [74]. Diet–microbiota interactions mediate epigenetics via modulating epigenetic mechanisms and establishing IBD-associated dysbiosis, which can result in an increased risk of CD and UC [74,75]. SCFAs produced by anaerobic gut microbial fermentation of dietary fibre-rich substrates may act as epigenetic mechanisms in regulating IBD-related inflammation through inhibiting cytokine production (e.g., IL-17), which plays a key role in the pathogenesis of IBD [76].

SCFAs, and butyrate and propionate in particular, regulate intestinal homeostasis and immune responses, not only via the inhibition of HDACs, but also by the activation of GPRs, including GPR41 (free fatty acid 3/receptor 3; FFA3/FFAR3) and GPR43 (FFA2/FFAR2) in macrophages and DCs, which enhance the differentiation of Tregs, characterised as the CD4+CD25+ Foxp3+ phenotype, and anti-inflammatory activities in colonic mucosa [76,77,78]. Modifications in DNA methylation in response to commensal microbiota and their metabolites (e.g., SCFA) may contribute to the maintenance of paediatric IBD via a variety of mechanisms [37]. UC patients with active disease display a significant decrease in total SCFAs, butyrate, propionate, and acetate concentrations, whereas patients in remission had higher butyrate concentrations compared with healthy counterparts [79]. Butyrate metabolism is the main down-regulated pathway associated with adult and paediatric UC, which reduces the gene expression levels of BDH2, ACSM3, EHHADH, and HMGCS2 in the intestinal mucosa of UC patients [80]. Butyrate has been shown to regulate mitochondrial gene expression associated with dual oxidase 2 (DUOX2) genotype-induced ROS, particularly the DUOX2 loss-of-function haplotype, which is implicated in paediatric CD ileal strictures [81]. Butyrate and propionate exert anti-inflammatory effects on the human intestinal enteroid (HIE)-derived monolayer by modulating adherent-invasive Escherichia coli (AIEC) virulence gene expression, implicated in the invasion of intestinal cells, while enhancing the integrity of the epithelial barrier, and reducing gut inflammation through downregulating cytokines TNF-α, IL-6, IL-8, and CXCL family gene expression [82]. A previous experimental study has shown that butyrate inhibits TNFα release and lipopolysaccharide (LPS)-induced IL-6 and IL-1β mRNA expression in the inflamed mucosa of adult CD patients via downregulation of the NF-κB pathway [83]. In an in vitro study relevant to IBD, butyrate and propionate were found to be more effective than acetate in inhibiting LPS-induced TNFα production from neutrophils and TNFα-mediated NF-κB activation in the human colon adenocarcinoma cell line [84]. The expression of SCFA receptor GPR43 identified on intestinal endocrine L-cells has been shown to be reduced in CD patients fed with high-fat/sugar diets [85]. It has been shown that GPR43 mediates the therapeutic activity of butyrate in IBD, in which butyrate exhibits a high potency barrier, enhancing activity in IECs, and inhibiting LPS-induced TNFα, IL-6, IL-1β and IFN-γ, IL-17 release in human peripheral blood mononuclear cells (PBMCs), which were all found to play a significant role in IBD development in children [86]. Butyrate and/or propionate play a significant role in the maintenance of human colon IECs by suppressing HDACs and NF-κB signalling in response to TLR activation [87,88]. In human colon IECs, butyrate suppresses HDACs, thereby promoting intestinal epithelial barrier function through hypoxia inducible factor-1 (HIF-1) and STAT3 activation, which regulate the integrity of epithelial tight junctions, and inhibiting LPS-induced NF-κB activation, which, in turn, decreases pro-inflammatory cytokines (e.g., IL-6, TNF-α, iNOS), while increasing anti-inflammatory cytokine (e.g., IL-10) expression [89]. This suggests that SCFAs, particularly butyrate, may serve as a key epigenetic metabolite that exhibits anti-inflammatory effects in IECs, providing a potential therapeutic role for paediatric IBD treatment via the mechanisms for epigenetic regulation.

7. KBs as Epigenetic Modifiers in IBD

βOHB administration on the colonic mucosa of IBD patients has been shown to increase levels of IL-4Ra- and IL-10-induced M2 macrophage polarisation through activation of the STAT6 signalling pathway [90]. βOHB increases histone lysine β-hydroxybutyrylation (Kbhb) in human embryonic kidney 293 (HEK293) cells, which is a type of histone posttranslational modification responsible for regulating gene expression and chromatin structure [91]. In vitro, βOHB inhibits HDAC1 and enhances histone H3 acetylation in macrophages through binding to GPCRs, which results in increased FOXP3+ gene expression and inhibited NOD-like receptor pyrin-domain containing-3 (NLRP3) inflammasome activation, which could, in turn, inhibit the expression of pro-inflammatory cytokines involved in IBD [71]. In human models, NLRP3 inflammasome, which is implicated in paediatric IBD [92], has been shown to be inhibited by βOHB, resulting in decreased pro-inflammatory cytokines IL-1β and IL-18 production in LPS-activated human monocytes with significantly increased histone H3 acetylation in macrophages [93]. HDAC1 is the major Kbhb deacylase in vitro, in which it reduces Kbhb levels in HEK293 cells [94]. In these cells, Kbhb levels on H3K4 residue, which are associated with the severity of inflammation in IECs in children [38], have been found to increase upon treatment with βOHB [94], suggesting that βOHB may have therapeutic potential in paediatric IBD, manifested in regulating gene expression profiles by increasing Kbhb levels in HEK293 cells. It can be suggested that βOHB as a potential epigenetic modifier exerts anti-inflammatory effects in IECs through its ability to attenuate intestinal inflammation and reduce damaged intestinal tissues in paediatric IBD.

8. Gut Microbiota-Derived SCFAs as Therapeutic Potential Agents in Paediatric IBD

This section aims to summarise the evidence supporting the therapeutic potential of gut microbiota-derived SCFAs in paediatric IBD.

8.1. Bifidobacterium and Lactobacillus spp.

Probiotic strains of SCFA-producing Bifidobacterium and Lactobacillus have been demonstrated to reduce IBD in human models by improving the intestinal epithelial barrier integrity and regulating the host immune response [95,96,97]. The most commonly used probiotics in RCT studies for the treatment of IBD were L.plantarum, L.acidophilus, L.actis, L.reuteri, L.delbrueckii subsp. Bulgaricus, B.breve, B.longum, B.infantis, and B.bifidum [98]. The bacterial abundance of Bifidobacterium and Lactobacillus spp. was reported to be reduced in paediatric IBD patients [16,17]. Several RCTs/experimental studies demonstrated the therapeutic potential of Bifidobacterium and Lactobacillus strains in IBD. The results of in vitro experiments showed that several strains belonging to the species, B.longum and L.plantarum, exert anti-inflammatory effects on IECs, as indicated by increased anti-inflammatory cytokine IL-10 and reduced TNF-α, NF-κB, IFN-γ, and pro-inflammatory cytokines (IL-2, IL-4, IL-6, IL-8, IL-17, IL-1β) production, which are involved in the pathogenesis of paediatric IBD [99,100]. Evidence from an in vitro experiment showed that probiotic supplementation with the B.longum strain BL05 in combination with the B.lactis BL04 and L.rhamnosus LR32 strains were able to modulate the immune inflammatory response of monocyte-derived M1 macrophage by increasing cytokine IL-10 and reducing the production of cytokines IL-6 and IL-1β [101]. Another recent experimental study showed that a mixture of four probiotic strains (including L.acidophilus LA1, L.paracasei 101/37, B.animalis spp. Lactis Bi1, and B.breve Bbr8) inhibit IL-8, IL-23, and IL-1β cytokine production in monocyte-derived dendritic cells (MoDC) from UC patients [102]. Treatment with B.bifidum NCC189 and S17, B.longum NCC2705, and B.lactis NCC362 has a potentially inhibitory effect on LPS-induced NF-κB activation and mRNA expression of TNF-α, IL-8, and cyclooxygenase 2 (Cox-2) in the IECs of IBD patients [103]. The administration of different probiotic strains of B.bifidum has been shown to enhance colonic acetate production in vitro, which exerts anti-inflammatory effects by inhibiting TNF-α expression [104]. B.bifidum strains (BbrY and BbiY) have been found to enhance cytokine IL-10 production and reduce cytokine IL-8 production in the PBMCs of UC patients [105]. Probiotic B.infantis 35624 and L.salivarius UCC118 strains exert anti-inflammatory effects on HT-29 human IEC by inhibiting Salmonella typhimurium (S.typhimurium)-induced TNF-α, NF-κB p65, cytokine IL-8 production, and increasing cytokine IL-10 production [106]. The treatment of HT-29 human IEC with B.bifidum strains (BGN4-SK and BGN4-pBESIL10) inhibits TNF-α and cytokine IL-8 production [107]. Treatment with L.brevis, L.pentosus, and L.curvatus reduces Salmonella-induced-IL-1β, IL-6, IL-8 mRNA levels and the p-IκB-α level, and increases cytokine IL-10 production and zonula occludens-1 (ZO-1)-mediated tight-junction integrity in HT-29 human IEC via the inhibition of the NF-κB pathway [108]. L.plantarum LM17 and L.rhamnosus LM07 strains exert anti-inflammatory activity in TNF-α-induced HT-29 human IEC by reducing cytokine IL-8 production [109]. L.kefiri strain CIDCA 8348 reduces TNF-α, IFN-γ, cytokines IL-6, IL-13 production, and increases cytokine IL-10 production and CD4+ FOXP3+ T cell expression in the inflamed mucosa of IBD patients [110]. Treatment with B.adolescentis ATCC 15703, B.longum ATCC 15697, and B.breve (ATCC 15700) strains has shown anti-inflammatory effects on macrophages in vitro by inhibiting LPS-induced TNF-α and IL-1β mRNA, while increasing IL-10 mRNA levels [111]. The administration of the B.longum strain, CECT 734, to children with newly diagnosed CD resulted in reduced serum TNF-α expression and peripheral CD3+ T lymphocytes [112]. The administration of the L.reuteri strain, ATCC 55730, to UC children has been shown to increase cytokine IL-10, and to reduce TNF-α and cytokines IL-8 and IL-1β production [113]. Taken together, these findings suggest that probiotic Bifidobacterium and Lactobacillus strains may have a therapeutic role in reducing paediatric IBD by their ability to exert anti-inflammatory effects in inhibiting inflammatory markers.

8.2. Bacteroides spp.

B.vulgatus and B.thetaiotaomicron are commensal butyrate-producing bacteria [114,115], with anti-inflammatory activity which may have a potential regulatory role in reducing inflammation in the context of paediatric IBD. The relative abundance of both bacteria has been found to be decreased in the gut mucosa-associated microflora of paediatric IBD [116]. Probiotic dietary supplementation with B.thetaiotaomicron is regarded as safe and tolerable in paediatric CD patients [117]. In one experimental study, B.vulgatus, compared to Escherichia coli (E.coli), failed to increase TNF-α-induced IL-8 production, as well as NF-κB transcriptional activity activation, in HT-29 human IEC in the presence of CD- and UC-derived PBMC [118]. In another recent experimental study, the isolated LPS from B.vulgatus, compared to that of E.coli LPS, exerted immunomodulatory effects as indicated by their ability to inhibit cytokines IL-6 and IL-8, NF-κB, TNF-α, and CXCL-8 production [119]. B.thetaiotaomicron produces nanosized outer membrane vesicles (OMVs), which serve a mediating role in microbe–host immune interactions, and exert anti-inflammatory activity in ILCs via increasing cytokine IL-10 production by colonic DC [120]. B.thetaiotaomicron attenuates intestinal inflammation via mechanisms related to the modulation of tryptophan metabolism in inflamed intestinal tissues. Particularly, B.thetaiotaomicron enhances the differentiation of anti-inflammatory Th1/Th17 cells by modulating CpG within the Foxp3+ promoter, thereby inducing Tregs differentiation [121]. This suggests that B.thetaiotaomicron and B.vulgatus may reduce intestinal inflammation in paediatric IBD patients by inhibiting inflammatory gene expression in IECs.

Although some strains of B.fragilis (e.g., enterotoxigenic B.fragilis) are enteric pathogens [122], other commensal strains detected on the inflamed colonic mucosa of CD and UC paediatric patients produce surface immunomodulatory capsular polysaccharide A (PSA) [123], which has been found in vitro to increase cytokine IL-10 production, inhibit LPS-induced monocyte TNF-α, and induce CD39+ Foxp3+ Tregs in a DC-dependent manner [124]. It has been shown that B.fragilis with a PSA on foetal enterocytes inhibits IL-1β-induced IL-8 production by binding to the TLR2 receptor on CD4 lymphocytes to promote the proliferation of FOXP3+ Tregs cells, resulting in increased IL-10 production [125]. B.fragilis during CD exacerbation produces virulent genes, such as bft (fragilysin), but this was found to induce IEC resistance rather than disrupting the barrier [126]. This suggests that B.fragilis may effectively reduce intestinal inflammation in paediatric IBD, but further studies are needed to evaluate its anti-inflammatory effects on IECs.

8.3. Faecalibacterium prausnitzii

F.praunsitzii is a commensal butyrate-producing bacterium which has a potential role in gut homeostasis and in promoting anti-inflammatory effects on human IECs [127]. The gut microbiota composition in paediatric IBD is characterised by low F.praunsitzii abundance [128,129]. Butyrate produced by F.praunsitzii exerts anti-inflammatory effects on in vitro PBMC and DC by reducing IFN-γ and cytokine IL-12 production, increasing cytokine IL-10 production [130,131], and inhibiting TNF-α and NF-κB activation in HT-29 human IEC [132]. F.prausnitzii was found to improve the barrier permeability of Caco-2 monolayers in vitro by increasing cytokine IL-10 production, while reducing the production of NF-κB and TNF-α, along with inflammatory cytokines such as IL-1β and IκBKβ [133]. F.prausnitzii induces human monocyte-derived and myeloid DC to prime CD4 T cells producing IL-10, induces Foxp3+ expression, and inhibits LPS-induced TNF-α and cytokine IL-12 production through modulating the TLR2/6 and c-Jun N-terminal kinase (JNK) signalling pathway [134]. Thus, F.praunsitzii may be involved in reducing inflammatory markers in IECs and producing anti-inflammatory effects in paediatric IBD.

8.4. Roseburia intestinalis

Gut microbiota dysbiosis in paediatric CD/UC patients is well known for its reduced abundance of butyrate-producing Roseburia spp. [17,135,136]. A significant depletion of Roseburia in IBD is likely associated with low levels of R.intestinalis, which is considered the most abundant species that has the ability to maintain gut homeostasis and induce anti-inflammatory responses through mechanisms for IBD regulation [137]. The relative abundance of R.intestinalis has been recently found to be decreased in paediatric CD and UC patients [138]. The R.intestinalis strain, DSM 14610, has been shown, in vitro, to breakdown oligofructose to produce butyrate, only by the presence of acetate produced by the B.longum strain, BB536, in the growth medium, suggesting a cross-feeding between R.intestinalis and B.longum [139]. In vitro studies have also shown that R.intestinalis DSM 14610 has the ability to produce butyrate in the presence of acetate produced by bifidobacterial strains [140]. Given the fact that R.intestinals is identified as a butyrate producer, strains of such species may be involved in inflammatory immune response regulation, and thereby a potential probiotic in the treatment of paediatric IBD. R. intestinalis was able to suppress gut inflammation by inhibiting LPS-induced IL-17 secretion and promoting Treg differentiation in colitis [141]. The R.intestinalis strain, DSM 14610, stimulates TGF-β mRNA secretion and promotes colonic Treg in LPS induced Caco-2 cells in CD patients [142]. The R.intestinalis strain, DSM 14610, alone or in combination with the F.prausnitzii strain, A2-165 (DSM 17677), and Bacteroides faecis (B.faecis) strain, DSM 24798, exerts beneficial anti-inflammatory effects on Caco-2 and HT29 cells in vitro by a significantly suppressed LPS cocktail of (IL-1β, TNF-α, IFN-γ)-induced claudin-2 protein expression [143]. Further in vitro studies are needed to assess the anti-inflammatory effects of R.intestinalis and the mechanisms behind its beneficial action in reducing paediatric IBD.

Figure 1 summarizes the mediating role of SCFAs in paediatric IBD therapy.

Figure 1

Role of SCFAs as a mediator in paediatric IBD therapy. (↓) decrease, (↑) increase.

9. Conclusions

Diet and other environmental factors may play a crucial role in establishing dysbiosis of the gut microbiota involved in the pathogenesis of IBD. SCFAs are considered the key epigenetic metabolites that mediate the relationships between the VLCKD and gut microbiota in children. SCFAs and βOHB may have the ability to induce epigenetic modifications in the inflamed colonic mucosa of paediatric IBD. Butyrate acts synergistically with βOHB to reduce intestinal inflammation in paediatric IBD and inhibit HDAC, reduce inflammatory cytokine production, and increase histone H3 acetylation in macrophages. SCFA-producing bacteria appear to have a significant role in promoting gut barrier integrity and reducing the production of inflammatory cytokines involved in paediatric IBD caused by a dysregulation of the colonic mucosa. The adherence to the VLCKD may result in increased SCFA-producing bacteria in paediatric IBD, including Bifidobacterium spp., Lactobacillus spp., Bacteroides spp., F.praunsitzii, and R.intestinalis. SCFA-producing probiotic Bifidobacterium and Lactobacillus strains may have beneficial effects in modulating immune responses in the inflamed mucosa of paediatric IBD patients. Butyrate-producing bacteria, including Bacteroides spp., F.praunsitzii, and R.intestinalis, may be a potential treatment for paediatric IBD due to their ability to reduce inflammation in IECs. Given that the VLCKD influences the gut SCFA-producing bacteria in children, it may have a potential role in inducing remission and mitigating inflammation in IBD, but further studies are needed to evaluate whether changes in the gut microbiota-producing SCFAs are associated with specific inflammation markers before, during, and after treatment with the VLCKD. Further studies of the VLCKD to assess its safety for the treatment in paediatric IBD patients are also needed.