This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Author contributions: Zheng L wrote and revised the manuscript; Zheng L and Wen XL designed the work and supervised preparation of the manuscript.
Supported byShaanxi Province Natural Science Basic Research Program-general Project, No. 2019JM-580; Project of Shaanxi Administration of Traditional Chinese Medicine, No. 2019-ZZ-JC0010; and Shaanxi Provincial Hospital of Traditional Chinese Medicine, No. 2018-04.
Conflict-of-interest statement: The authors declare that there are no conflicts of interest.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Xin-Li Wen, Director, Professor, Department of Gastroenterology, Shaanxi Provincial Hospital of Traditional Chinese Medicine, No. 4 Xihuamen, Xi’an 730000, Shaanxi Province, China. firstname.lastname@example.org
Received: October 18, 2020 Peer-review started: October 18, 2020 First decision: November 20, 2020 Revised: November 20, 2020 Accepted: December 6, 2020 Article in press: December 6, 2020 Published online: January 16, 2021
Inflammatory bowel disease (IBD) is a chronic immune-mediated disease that affects the gastrointestinal tract. It is argued that environment, microbiome, and immune-mediated factors interact in a genetically susceptible host to trigger IBD. Recently, there has been increased interest in the development, progression, and treatment of IBD because of our understanding of the microbiome. Researchers have proved that some factors can alter the microbiome and the pathogenesis of IBD. As a result, there has been increasing interest in the application of probiotics, prebiotics, antibiotics, fecal microbiota transplantation, and gene manipulation in treating IBD because of the possible curative effect of microbiome-modulating interventions. In this review, we summarize the findings from human and animal studies and discuss the effect of the gut microbiome in treating patients with IBD.
Core Tip: Inflammatory bowel disease (IBD) is a chronic immune-mediated disease that affects the gastrointestinal tract. Researchers have proved that some factors can alter the microbiome and the pathogenesis of IBD. These include mutations in genes involved in microbiome-immune interactions and microbiota-modulating risk factors such as antibiotic use, cigarette smoking, levels of sanitation, and diet. As a result, there has been increasing interest in the application of probiotics, prebiotics, antibiotics, fecal microbiota transplantation, and gene manipulation in treating IBD because of the possible curative effect of these microbiome-modulating interventions.
Citation: Zheng L, Wen XL. Gut microbiota and inflammatory bowel disease: The current status and perspectives. World J Clin Cases 2021; 9(2): 321-333
Various microbial organisms are found in the gut, with the number exceeding 100 trillion, including bacteria, fungi, viruses, as well as protozoa[1,2]. The number of bacteria varies throughout the entire gastrointestinal tract, making a comparison between the colon, stomach, and small intestine difficult as the amount and diversity of bacterial species are higher in the colon[3,4]. In humans, homeostasis of nutrition, immune development, metabolism, and defense against pathogens is essential, and it is achieved because of the existence of the gut microbiome.
MICROBIOME AND INFLAMMATORY BOWEL DISEASE
Inflammatory bowel disease (IBD) is a chronic immune-mediated disease. Based on the analysis of numerous animal models, alteration or an aberrant immune response occurs in the microbiome, which may lead to intestinal inflammation. When pro-inflammatory bacteria or microbiota are transferred from mice with IBD to healthy mice, inflammation is triggered, and colonization of intestinal microbiota in mice from donors with IBD exacerbates colitis by altering immune responses[7,8]. In human subjects, it was observed that the microbiome plays a fundamental role in the occurrence of IBD. In addition, during treatment of Crohn’s disease (CD), fecal diversion has been proved to be a valuable technique, as disease severity is reduced due to exclusion of the affected bowel segment. It has been shown that antibiotics are effective in treating certain phenotypes of IBD. Recently, studies have demonstrated that specific microbes may drive or suppress inflammation, predict response to therapy, and determine the postoperative risk of disease recurrence so as to provide evidence for the curative effect of the microbiome in treating patients with IBD[12,13] (Table 1).
Table 1 Microbiota changes associated with inflammatory bowel disease.
Genetic susceptibility plays a key role in the etiology of IBD. A recent study involving 75000 patients has identified 163 susceptibility loci for IBD, and most of them participated in regulating the interaction between host and gut microbes[15,16].
The nucleotide-binding oligomerization domain-2 (Nod2) gene was initially reported as a susceptibility gene for CD. Nod2 is predominantly expressed in Paneth cells of the ileum and can induce immune responses under the stimulation of intestinal flora. The number of mucosa-adherent bacteria increases in IBD patients carrying Nod2 mutations. Patients with Nod2 mutations have characteristic changes in gut flora when compared with patients without Nod2 mutations: Enterobacter species increase, and Faeculus species decrease. In addition, abnormal aggregation of goblet cells and lymphocytes and expression of inflammatory factors can be found in the intestines of Nod2-/- mice. Compromised intestinal barrier function is associated with the imbalance of the intestinal flora, especially the increase of Bacteroides vulgaris, and downregulating the abundance of Bacteroides vulgaris can reverse the barrier defect in Nod2-/- mice.
Mutations in autophagy-related genes are associated with increased risk of CD. IBD patients with both autophagy-related gene 16L1 mutation and Nod2 mutation have significant changes in intestinal flora, including decreased abundance of Faebacterium and increased abundance of Escherichia coli. Selectively knocking out the ATG16L1 gene in mice can down-regulate the number of regulator T (Treg) cells and T helper (Th)2-mediated cellular immunity. The abnormal immune effect makes the intestine lose its tolerance to intestinal pathogens and produce immunoglobulins that attack the intestinal commensal bacteria, leading to intestinal flora imbalance. In a recent study, feces from patients with active CD were transplanted into sterile ATG16L1-deficient mice, which induced the increase of Bacteroides ovatus and the increase of Th17 and Th1 immune cells in intestinal lamina propria, suggesting the effects of gene polymorphisms on IBD rely on the role of intestinal flora.
Glycoprotein CLEC7A, a pattern-recognition receptor expressed by innate immune cells, can mediate the interaction between fungi and intestinal immune system. The intestinal fungal community changed in CLEC7A-deficient mice, along with increased susceptibility to enteritis. Knockout of caspase recruitment domain-containing protein 9 (CARD9) gene, a downstream molecule of CLEC7A, can also cause changes of the intestinal fungal microecology in mice and increase the susceptibility of mice to dextran sodium sulfate-induced enteritis. Imbalance of fungal gut flora caused by CARD9 deficiency is closely related to the lack of intestinal Th17 cells. Lanternier et al also found that the colonization of Malassezia could increase the severity of CD, and such inflammatory response induced by the fungal colonization was associated with the genetic polymorphisms of CARD9.
Although intestinal flora imbalance plays a key role in the etiology of IBD, change of intestinal flora alone does not cause enteritis. Research on genetic polymorphisms reveals the important role of individual differences in the pathogenesis of IBD. The polymorphism of individual genes can affect the structure of the intestinal flora, and the imbalanced intestinal flora can further activate the immune system and induce intestinal inflammation in the context of genetic susceptibility.
MECHANISMS OF IMMUNE DISORDERS INDUCED BY INTESTINAL FLORA IMBALANCE IN IBD
Intestinal flora imbalance and gene polymorphisms play key roles in the pathogenesis of IBD, although both of them depend on the intestinal immune microenvironment. Physiologically, there is a symbiotic relationship between intestinal microorganisms and the host, and this relationship depends on a variety of immune mechanisms such as the secretion of immunoglobulin (Ig) A from the intestinal mucus and the release of antimicrobial peptides[28,29]. In addition, intestinal symbiotic bacteria can also inhibit the growth of pathogenic microorganisms, promote immune tolerance, initiate intestinal epithelial repair, and maintain the balance among various immune cell subtypes. In patients with IBD, however, the unregulated intestinal microecology, together with the body’s susceptibility genes, induces abnormal immune responses and causes disorders of the intestinal immune microenvironment.
With regard to humoral immunity, the antibodies secreted by different intestinal microorganisms are closely related to the phenotypes and course of IBD. Research showed that the combination of anti-Saccharomyces cerevisiae mannan antibodies with anti-laminaribiose antibodies and anti-neutrophil cytoplasmic antibodies helped to distinguish IBD patients, non-IBD patients, and healthy individuals. The levels of these three antibodies significantly differ between CD and ulcerative colitis (UC) patients. In addition, as the most important antibody in the intestinal mucosa, IgA has an encapsulation effect on microorganisms and thus is a marker for the immune response activated by gut microbes. These IgA-encapsulated gut microbes can be divided into enteritis IgA+ bacteria and intestinal symbiotic IgA-bacteria, among which the IgA+ bacteria include Prevotellaceae, Helicobacter, and segmented filamentous bacteria. These bacteria can participate in dextran sodium sulfate-induced enteritis in mice. Furthermore, IgA deficiency also increases the risk of CD and UC development[36,37].
In terms of cellular immunity, gut microbes play an important role in maintaining T cell function. Gut microbes can induce T cells to differentiate into Th17, Treg cells, and other phenotypes by shaping the intestinal microenvironment. The segmented filamentous bacteria colonizing the small intestine of mice can adhere to the epithelial cells of the small intestine and induce Th17 cells in the intestinal lamina propria to secrete interleukin (IL)-17 and IL-22, thus promoting intestinal inflammation. On the contrary, some intestinal bacteria promote the proliferation of anti-inflammatory Treg cells. The colonization of clostridium in the intestines of mice can increase the intestinal transforming growth factor-β level, thereby promoting the differentiation of Foxp3+ Treg cells. Research has shown that the intestinal bacteria derived from IBD patients can induce the increase of Th17 and Th2 cells and the decrease of RORγt+ Treg cells in the mouse intestines. After feces from healthy people were transplanted into mice, a consortium of 11 bacterial strains that induced interferon-γ-producing CD8 T cells in the intestine was isolated, which could relieve intestinal inflamm-ation.
In the intestinal immune microenvironment, antigen-presenting cells can not only deliver gut bacteria-related antigens but also regulate intestinal immune effector cells. When intestinal commensal bacteria adhere to epithelial cells, CX3CR1+ antigen-presenting cells secrete IL-10 under the action of intestinal bacteria antigens to induce Treg cell differentiation, thus maintaining a balanced pro- and anti-inflammatory environment in the gut. However, when the intestinal flora becomes imbalanced, CX3CR1+ antigen-presenting cells can induce Th1 immune cells to mediate intestinal inflammation. In addition, Ruminococcus gnavus, which is closely related to CD, can act on toll-like receptor 4 receptors in dendritic cells by secreting polysaccharides, thus inducing the secretion of tumor necrosis factor-α, a proinflammatory cytokine. Macrophages are also important antigen-presenting cells in the intestinal mucosal barrier. Intestinal bacteria can induce macrophages to secrete IL-1β through the Nod2-Myd88 signaling pathway to mediate intestinal inflammation. However, intestinal Helicobacter hepatica can activate the mitogen activated protein kinase/cyclic adenosine monophosphate response element-binding protein through the toll-like receptor 2 receptor of macrophages to promote the secretion of IL-10 and participate in the anti-inflammatory response in the intestine.
MICROBIAL COMPOSITION AND FUNCTION IN PATIENTS WITH IBD
Decades ago, it was first confirmed that the fecal stream containing bacteria was associated with IBD when surgical diversion was used to induce remission of diseased segments; when continuity was restored, these patients may develop IBD recurrence. A large number of studies have indicated that alterations in the composition of gut microbiota are associated with IBD. As a result, more and more research has focused on the diagnostic and prognostic potential of microbiota signatures in patients with IBD.
Metagenomics of the gut microbiota in patients with IBD
Although the interaction between intestinal microecology and the body can regulate the intestinal immune microenvironment, the exact mechanisms remain unclear. As the intestinal flora changes, the intestinal metabolites in IBD patients also change. Compared with healthy individuals, IBD patients have remarkably altered intestinal mucosal, fecal, and serum metabolites.
Short-chain fatty acids (SCFA, mainly including butyrate, propionate, and acetate) are the primary products of the breakdown of non-digestible carbohydrates by gut bacteria. Among them, butyrate, which is produced by Clostridium, can inhibit histone deacetylase by activating G protein-coupled receptors and epigenetic effects, thereby enhancing the function of mucosal Treg cells and alleviating enteritis in mice. The increase in butyrate can also promote the proliferation of Treg cells by inhibiting deacetylase, suppress the Th17-mediated immune response, and promote the secretion of IL-6 in macrophages, thus exerting its protective effect on the gut. As an agonist of peroxisome proliferator-activated receptor γ, butyrate can also inhibit the synthesis of nitric oxide and the degradation of nitrate in gut, thereby suppressing the proliferation of Enterobacteriaceae. However, the abundance of SCFA-producing bacteria dramatically decreases in the feces of IBD patients, leading to a decrease in intestinal SCFA levels and an increase in intestinal inflammation.
Tryptophan can be converted into biologically active indole metabolites by intestinal bacteria. Studies have shown that there were significant differences in the serum levels of tryptophan metabolites between normal mice and sterile mice, and indole derivatives, which are the metabolites of tryptophan, can also mediate host inflammation. The intestinal commensal Peptostreptococcus can produce indole propionic acid, a special indole derivative, to induce mucin gene expression and activate the nuclear factor E2-related factor 2 pathway, thus exerting its effect in alleviating intestinal inflammation. Bacteroides can metabolize tryptophan into serotonin, the precursor for melatonin, and serotonin can exhibit multiple effects by binding to different serotonin receptors, especially the regulation of intestinal inflammation. However, the metabolism of tryptophan by intestinal bacteria decreases in IBD patients, resulting in the disturbances in intestinal microenvironment and the development of enteritis.
The bile acids produced by the metabolism of intestinal flora can act as agonists of G protein-coupled receptors and farnesoid X receptors. They can regulate host genes, thereby regulating the maturation of immune cells, the release of cytokines, and the defense against microorganisms. Taurine is a secondary bile acid derived from the decomposition of primary bile acid. It can increase microbial diversity by regulating the function of inflammasomes. Clostridium can also regulate bile acid metabolism through dehydroxylation and inhibit the intestinal Clostridium difficile infection. In addition, conjugated bile acids can also up-regulate the expression of exogenous transporter multidrug resistance protein 1 in CD4+ effector T cells to maintain the homeostasis of the body. However, the expression of multidrug resistance protein 1 dramatically declines in IBD patients.
Sphingomyelin is a class of plasma membrane-associated lipids produced by the host and specific bacteria. The cell level and distribution of sphingomyelin significantly differ between inflammatory tissue and non-inflammatory tissue in IBD patients. The colonization of Bacteroides polymorpha in sterile mice could maintain the balance of the intestinal environment; however, the colonization of mutant strains without the function of synthesizing sphingomyelin in the intestine caused the increase of IL-6 and monocyte chemotactic protein 1 and thus induced enteritis. Metabonomic studies have also found that the abundance of sphingomyelin derived from Bacteroides was low in IBD patients; as the abundance of sphingomyelin in the body decreased, the inflammatory response tended to rise.
Meta-transcriptomics of the gut microbiota in patients with IBD
Some researchers have focused on the functional activity (meta-transcriptomics) instead of the functional potential (metagenomics) of gut microbiota in patients with IBD, and for both there is no accurate correlation. For example, when comparing patients with UC or those with CD to healthy control subjects, the RNA level in the patient groups was markedly lower than that in the healthy group, while the change in abundance of deoxyribonucleic acid (DNA) increased slightly. This indicated that the patients with IBD may be significantly affected by minor alteration in R. gnavus abundance at the DNA level. Furthermore, when comparing patients with UC and healthy control subjects, it was found that the abundance of B. fragilis DNA was much lower than that of RNA. Consequently, based on the results between patients with UC and healthy control subjects, a decreasing trend in both the functional potential and activity of B. fragilis was observed. F. prausnitzii, B. vulgatus, and Alistipes putredinis were found to contribute significantly to metabolic pathway transcription in patients with IBD, even when they were not the most abundant organisms present. In order to confirm these results, Clostridium hathewayi, C. bolteae, and R. gnavus and their genomic abundance were compared, and it was found that the transcriptional activity of C. bolteae and R. gnavus in patients with IBD was significantly increased, which indicated that they possibly play a more significant role.
Metabolomics of the gut microbiota in patients with IBD
According to the results of a few studies, it is suggested that patients with IBD have a depletion of biologically active and functionally important metabolites. In addition, SCFA are important anti-inflammatory bacterial metabolites, which are decreased in the bacteria that can produce metabolites in these patients. SCFA plays a role in providing energy for colonic epithelial cells and promoting the expansion of regulatory T cells in the colon. Furthermore, in these patients, the level of SCFA, including butyrate, as well as the secondary bile acids lithocholate and deoxycholate decreased. Generally, patients with IBD show no deficiencies in sera, but it should be noted that the vitamins pantothenate (vitamin B5) and nicotinate (vitamin B3) were particularly depleted in the gut. Nicotinate is characterized by its anti-inflammatory and antiapoptotic features. It was noted that other metabolites including sphingolipids and carboximidic acids were overabundant in patients with CD. B. fragilis, which is involved in synthesizing sphingolipids and has a similar structure to invariant natural killer T (iNKT) cell agonists, was shown to play a role in reducing iNKT cell activation and expansion triggered by self and microbial stimuli in neonatal mice. As a result, when the neonate grew, the iNKT cell numbers reduced, and experimentally-induced colitis was prevented. During inflammation, the oxygen concentration may become higher; thus, this environment is poisonous to obligate anaerobes and may lead to a diminished mucus layer.
Role of F. prausnitzii in patients with IBD
Among the variety of bacteria mentioned above, more and more attention has been focused on the relationship between F. prausnitzii and the pathogenesis of IBD. Some studies have described the low abundance of anti-inflammatory Firmicutes, and this may increase the risk of recurrence of ileal disease after surgery. In addition, it was observed that when F. prausnitzii in stool was at a low level, CD relapse in patients in remission could be predicted. Furthermore, F. prausnitzii was protective in dinitrobenzene sulfonic acid-induced colitis in mice. Research has shown that microbial anti-inflammatory molecule (MAM), a special protein produced by F. prausnitzii, can resist inflammation and inhibit the nuclear factor k B pathway in epithelial cell lines. L. lactis, used to deliver a plasmid encoding the MAM protein, is effective in preventing dinitrobenzene sulfonic acid–induced colitis in mice.
VIRUSES IN PATIENTS WITH IBD
Enterovirus is closely related with IBD. It was found that bacteriophages were significantly increased in the colon tissue of CD patients compared with that of healthy individuals. A viromic study demonstrated that the viromic status of CD patients was related to both disease status and treatment. Although individual differences and sample sources have a greater impact on the viromic status than on CD, it has also been found that there were more viruses in the virome of CD patients than in healthy people, and the diversity of viruses in the feces and intestinal tissues of newly diagnosed patients was higher than that in relapsed patients. It is still unclear whether the decrease in bacterial abundance and the increase in phage abundance are associated with the onset of IBD. Although there are some common viruses in the virome of patients with CD or UC, there are also some unique disease-related phages, such as the phages of Lactococcus, Lactobacillus, Clostridium, Enterococcus, and Strepto-coccus.
IBD patients carry more mammalian viruses and human pathogens than healthy individuals, and human endogenous retrovirus (HERV) has also been found in the virome of IBD patients. The expression of HERV protein is related to inflammation. HERV expression is even higher in IBD patients infected with herpes virus. The significance of such correlation for IBD is unclear; however, infection with other viruses may also trigger HERV expression.
MICROBIOTA-BASED STRATEGIES IN PATIENTS WITH IBD
It is beneficial in patients with IBD to use several methods to regulate the gut microbiota during therapy. For example, when a deficit is identified in anti-inflammatory bacteria, such as F. prausnitzii, anti-inflammatory molecules produced by bacteria, such as MAM protein in the case of F. prausnitzii, can be augmented or administered. In this situation, probiotics, prebiotics, and synbiotics can be applied to replenish anti-inflammatory bacteria and their substrates. Another method is to identify the inflammatory bacteria that are overexpressed or toxic, and then antibiotics or phage therapy can be administered to remove the inflammatory bacteria. Fecal microbiota transplantation (FMT) can reset the whole microbiome. Research has shown that the microbiota can be used to deliver medications, for instance, modified organisms that are designed to release anti-inflammatory cytokines or other molecules that can directly reach the site of inflammation. The microbiome-immune interface has multiple targets that should be studied in further investigations.
Probiotics are a class of live microorganisms. They have shown good efficacy for IBD in animal experiments but have unsatisfactory effectiveness in clinical trials. No definite evidence supports the efficacy of probiotics in the treatment of CD, but these products may be effective in treating UC patients. Probiotics have certain effects in inducing and maintaining remission in UC patients. Positive research results have been achieved in patients with UC, but due to limitations in study design, availability of effective strains, as well as problems associated with the quality control of available probiotic preparations, the application of these findings in everyday practice may take some time. It has been confirmed that probiotics can be used to prevent primary and secondary pouchitis. The probiotic preparation that is effective in pouchitis, VSL#3, is a mixture of four strains of Lactobacillus species, three strains of Bifidobacterium species, and Streptococcus salivarius, and it increases the amount of mucosal regulatory T lymphocytes and decreases the mucosal expression of pro-inflammatory cytokine IL-1b messenger ribonucleic acid. To some extent, probiotics can maintain remission in patients with mild-to-moderate UC, even though they have varied curative effects. It has been found that probiotics are not effective in patients with CD. Due to the composition of specific probiotic preparations used to treat patients with IBD, the results have been varied. Therefore, it is possible that the unsatisfactory efficacy of probiotics may be because there is no ideal composition, duration of therapy is insufficient, or the intervention is too late when the ‘‘pathogenic’’ microbiota is already present. Studies are required on individualized and personalized therapy in particular IBD phenotypes, including designing probiotics for specific microbial changes.
Studies have shown that childhood antibiotic exposure increases the risk of IBD, and younger age of exposure and longer antibiotic use are associated with higher incidence of IBD. Antibiotics are not the first-line treatment for IBD, unless co-infection is considered. However, antibiotics have shown certain efficacies in some clinical trials. A meta-analysis shows that the combination of antibiotics can, to a certain extent, improve the clinical symptoms of IBD patients. Using ciprofloxacin to treat patients appears to result in remission, and although treatment responses were more frequent, the results were not statistically significant. Experiments have been conducted to evaluate the effect of metronidazole in preventing recurrence of CD after small intestinal resection, but no significant effect was obtained compared with biologic therapy. Following colectomy with ileal pouchanal anastomosis, the microbiome is crucial for driving inflammation in the ileal pouch. Only after the fecal stream is restored through the pouch may pouchitis occur. A study involving 16 subjects who received ciprofloxacin or metronidazole for 2 wk showed that pouchitis was resolved in all subjects who receive ciprofloxacin therapy and in 76% of subjects who received metronidazole therapy according to the pouchitis disease activity score. In conclusion, antibiotics show efficacy in the treatment of IBD, but there are few reports in the literature to validate this finding.
Diet is closely related to the compositions of intestinal flora and microbial metabolites. IBD patients were found to have dysregulated intestinal microbiota and decreased floral diversity, including an increase in Enterococcus and a decrease in the abundance of Firmicutes and Bacteroides. Similar changes in the abundance of intestinal flora have also been seen in some healthy people who embark on a low-carb, high-fat diet, indicating that fiber intake reduces the risk of CD, which may be related to the altered intestinal microbiota in genetically susceptible people. In a recent randomized controlled trial involving pediatric patients with CD, there was no difference in the remission rate between the group receiving partial enteral nutrition and the group receiving exclusive enteral nutrition. These findings indicate that the rebound effect may occur in subjects when they switch to a regular diet; thus, the score for the microbiome composition may return to the baseline level. A study conducted by Guo et al assessed the effect of different diets, such as diets low in red meat and processed meat, in preventing symptomatic relapse of CD. Thus, more randomized controlled trials determining the effect of diet therapy in the treatment of patients with CD are required in order to determine the benefit of different diet therapies.
FMT, also known as stool transplantation or bacteriotherapy, has been a research hotspot in recent years. It transfers gut microbes from a healthy donor into the gastrointestinal tract for the purpose of restoring the balance of gut microbes. FMT is particularly successful in the treatment of refractory Clostridium difficile infection. A meta-analysis showed that the clinical response rates of FMT for UC and CD were 21% and 30%, respectively. In another study, the clinical response rate of FMT was 20.9% in treating patients with mild to moderate IBD and 32.3% in patients with moderate to severe IBD. Thus, FMT was more effective in treating patients with moderate to severe IBD, suggesting that FMT may be used as a rescue treatment for refractory IBD. However, the heterogeneity of the currently available studies is high, mainly due to differences in transplantation methods and routes, selection of fresh or frozen feces, and selection of donors. Paramsothy et al have shown that FMT increased the diversity of the intestinal flora and changed the composition of the flora. Eubacterium hallii in fecal and colon samples was more abundant in patients who benefitted from FMT, while these results were not observed in patients who did not benefit. Donor stool containing Bacteroides species was associated with remission. However, Streptococcus species in donor stool was related to no response to FMT. Further studies are necessary to determine better methods for choosing donors to target the microbiome changes in patients with IBD in order to promote the curative effect of FMT.
According to the results from animal models, the microbiome can trigger IBD and even make it worse. Clinical data have shown that the microbiome is effective in CD therapy, but the effect is limited. According to recent studies, antibiotics are used to prevent postoperative recurrence of CD and to treat pouchitis and perianal disease.
Some probiotics may be beneficial for preventing pouchitis and in maintaining remission in patients with mild to moderate UC. Diet therapy is also considered to be helpful, especially in children with CD who receive exclusive enteral nutrition. However, further studies on adult patients, especially those with UC, are necessary. To date, only a few studies have provided support for FMT in treating UC, but there is little evidence for FMT in treating patients with CD. In conclusion, the microbiome is an exciting target for the treatment of IBD in future studies.
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Specialty type: Medicine, research and experimental
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