Several new drugs have been introduced into clinical IBD therapy in the past few decades that have helped to reduce corticosteroid use (e.g. anti-TNF and anti-integrin agents)
A large unmet need for novel therapeutic approaches exists, as many patients do not respond to the clinically approved drugs, including TNF blockers and vedolizumab
Many new therapeutic approaches have been developed based on studies in IBD mouse models, analyses of IBD tissues and new insights into inflammatory pathways in other chronic inflammatory disorders
Cytokine blockers (such as ustekinumab and JAK inhibitors) suppressing cytokine signalling are probably a new addition to our future clinical armamentarium for patients with IBD
New therapeutic concepts might enable achievement of new strict end points in IBD therapy, including mucosal healing, deep remission, transmural healing and histological healing
Identification of biomarkers to predict and monitor therapeutic success will be crucial to enable individualized therapy
Various therapeutic advances have led to a paradigm shift in the clinical management of patients with IBD. The introduction of immunosuppressive (such as azathioprine) and biologic agents (such as TNF blockers) has markedly reduced the need to use corticosteroids for therapy. Furthermore, the α4β7 integrin blocker vedolizumab has been introduced for clinical IBD therapy. Moreover, various new inhibitors of cytokines (for example, IL-6–IL-6R and IL-12–IL-23 blockers or apremilast), modulators of cytokine signalling events (for example, JAK inhibitors or SMAD7 blocker), inhibitors of transcription factors (for example, GATA3 or RORγt) and new anti-adhesion and anti-T-cell-activation and migration strategies (for example, β7 integrin, sphingosine 1-phosphate receptors and MAdCAM1 inhibitors, regulatory T-cell therapy and stem cells) are currently being evaluated in controlled clinical trials. This Review aims to provide a comprehensive overview about current and future therapeutic approaches for IBD therapy. Furthermore, potential mechanisms of action of these therapeutic approaches and their implications for clinical therapy in IBD are discussed.
Inflammatory bowel diseases (including IBD, exemplified by Crohn's disease and ulcerative colitis) are chronic relapsing disorders affecting the gastrointestinal tract. IBD has a progressive and destructive nature and, therefore, can cause various complications including stenoses, abscesses, fistulas, extraintestinal manifestations and colitis-associated neoplasias and cancer1,2. Thus, effective therapeutic approaches are of high clinical relevance in patients with IBD. This Review summarizes current therapeutic strategies and highlights emerging new treatment approaches for IBD with special reference to the proposed molecular mechanisms of action of anti-inflammatory drugs.
Current IBD therapies
Classic anti-inflammatory drugs. 5-Aminosalicylates (5-ASAs) are important anti-inflammatory drugs that are frequently used for anti-inflammatory therapy in patients with ulcerative colitis3. By contrast, 5-ASA-based drugs show little or no efficacy in inducing resolution of clinical symptoms and tissue inflammation in patients with Crohn's disease4.
5-ASAs are effective for induction and maintenance of remission in ulcerative colitis and might also reduce the risk of developing colitis-associated tumours in these patients5. Several mechanisms of action for 5-ASAs have been proposed, including reduction of prostaglandin synthesis via inhibition of cyclooxygenase, suppression of proinflammatory cytokine production and oxygen-free radicals, inhibition of lipoxygenase, blockade of neutrophil chemotaxis and mast cell activation, and impairment of nuclear factor-κB activation (NF-κB) in immune cells3. Moreover, studies in mice revealed that 5-ASA-based drugs augment peroxisome proliferator-activated receptor-γ (PPARγ) expression and promote PPARγ translocation from the cytoplasm to the nucleus where they result in activation of peroxisome-proliferator hormone response element-driven genes to suppress colitis activity6,7.
In addition to 5-ASAs, corticosteroids (systemically or topically delivered) have been used for remission induction in ulcerative colitis2. Although corticosteroids favour induction of remission in both ulcerative colitis and Crohn's disease, they are not suitable for maintenance of remission in IBD1,2. Mechanistically, glucocorticoids bind to a specific cytosolic receptor followed by translocation of the complex to the nucleus to either activate or repress gene transcription (via binding to DNA corticosteroid-response elements)8,9. Additionally, the glucocorticoid–receptor complex can inactivate proinflammatory transcription factors such as NF-κB and activator protein 1 (AP1) via protein–protein interactions, thereby preventing their activation of inflammatory mediators (for example, leukotrienes and cytokines such as IL-1 and IL-6).
Classic immunosuppressive drugs. Classic immunosuppressive drugs for IBD therapy include azathioprine or 6-mercaptopurine10,11,12,13,14, methotrexate15 and ciclosporin-A or tacrolimus16. The latter drugs have been used in studies for induction of remission in patients with ulcerative colitis, methotrexate has been used for induction and maintenance of remission in Crohn's disease and azathioprine is frequently used for maintenance of remission in both Crohn's disease and ulcerative colitis14,15,17. Several in vitro and in vivo studies have highlighted the potential mechanism of action of these drugs. Ciclosporin-A and tacrolimus bind to specific intracellular receptors (immunophilins) and act by blocking the activation of the transcription factor nuclear factor of activated T cells (NFAT) that controls cytokine gene transcription and apoptosis resistance of lymphocytes18,19. Moreover, methotrexate affects survival of immune cells by blocking cell proliferation and inducing apoptosis20. This drug also increases endogenous adenosine release, alters expression of cellular adhesion molecules and suppresses production of proinflammatory cytokines21. Finally, azathioprine and 6-mercaptopurine are metabolized to 6-thioguanine triphosphates that bind to the small GTPase RAC1, thereby suppressing the guanine exchange activity of VAV1 on RAC1 (Refs 10,11,22). Thus, RAC1 activation is suppressed, leading to inhibited activation of cells in both the innate and adaptive immune systems. In T cells for instance, azathioprine and 6-mercaptopurine can cause apoptosis through RAC1 inhibition10. Furthermore, T-cell apoptosis has been shown to correlate with responsiveness to azathioprine or 6-mercaptopurine in patients with IBD10.
Biologic therapy with anti-TNF agents. As many patients with IBD were either refractory or intolerant to treatment with the classic agents already discussed, there was an urgent need for the development of more specific novel therapeutic approaches. In this context, anti-TNF agents, including infliximab, adalimumab, golimumab and certolizumab pegol, were introduced into clinical therapy for IBD14,23,24,25,26,27,28,29,30,31,32,33. For instance, infliximab was shown to be effective for induction and maintenance of remission in both Crohn's disease and ulcerative colitis as well as for treatment of fistulas in Crohn's disease, highlighting the broad relevance of anti-TNF therapy14,24. In 2015 and 2016, infliximab biosimilars — biological products that are highly similar in structure and clinical efficacy to an already FDA-approved biological reference product — were approved for clinical therapy and adalimumab biosimilars are currently under development34.
Anti-TNF agents such as infliximab can be combined with immunosuppressive agents such as azathioprine in IBD. In fact, prospective clinical trials14,35 showed that combination therapy with infliximab and azathioprine is superior to induce corticosteroid-free clinical remission than monotherapy with either agent in both Crohn's disease and ulcerative colitis. Further studies indicated that initiation of more intensive treatment early in the course of the disease could result in improved outcomes36,37. Specifically, early combined immunosuppression (so-called top-down therapy with early azathioprine plus infliximab followed by de-escalation if possible) reduced the risk of major adverse outcomes in Crohn's disease as compared with conventional management (so-called step-up therapy: first corticosteroids, followed, in sequence, by azathioprine and then infliximab). Although early combined immunosuppression was not associated with an increased risk of serious drug-related adverse events or mortality in several studies34,37, future studies will have to determine the risk of adverse events of long-term combined immunosuppressive therapy. The described combination therapy with immunosuppressive agents and TNF antagonists is probably the best strategy for achieving optimal outcomes in patients at high risk of disease progression (for example, fistulizing or extensive disease). However, long-term prospective studies are still needed to understand the value of early combination therapy to prevent bowel damage, loss of gastrointestinal tract function and permanent disability38.
TNF is produced by various immune and non-immune cells in the inflamed gut of patients with IBD, including macrophages, T cells, dendritic cells, fibroblasts and fat cells39. This cytokine has pleiotropic effects in the bowel wall: it induces neoangiogenesis40; activates macrophages to produce proinflammatory cytokines; favours Paneth cell death via necroptosis41; augments apoptosis of intestinal epithelial cells42; regulates T-cell apoptosis40,43,44; and reduces production of tissue inhibitor of matrix metalloproteinases (MMPs) by fibroblasts to mediate tissue injury via activated MMPs45. Thus, anti-TNF antibodies can suppress intestinal inflammation in IBD through several mechanisms.
However, the anti-TNF agent etanercept has shown no efficacy in patients with Crohn's disease46, suggesting differences among anti-TNF drugs. Several potential explanations for this observation have been suggested. First, differences in tissue degradation of anti-TNF antibodies were found. After MMP3 and MMP12 induced proteolytic degradation, cleaved infliximab and adalimumab functioned as F(ab')2 fragments, whereas cleaved etanercept lost its ability to neutralize TNF47. This finding suggests that rapid MMP-induced degradation of etanercept might limit its capacity to block TNF in the inflamed mucosa in IBD. Second, only full IgG1 monoclonal anti-TNF antibodies such as infliximab and adalimumab were found to induce regulatory macrophages with wound-healing potential via Fc receptor signalling, suggesting that etanercept might fail to regulate macrophage function in IBD48. Third, in comparison to other TNF blockers, etanercept has a lower affinity to transmembrane TNF49. Membrane-bound TNF, however, is an important co-stimulatory signal for TNFR2 on mucosal T cells in IBD and mediates their resistance to apoptosis43. Thus, other TNF blockers might more effectively induce T-cell apoptosis than etanercept and such apoptosis induction has been shown to correlate with clinical responses to anti-TNF therapy in vivo44. Consistently, the presence of membrane-bound TNF on mucosal immune cells in vivo has been identified as a predictor of response to subsequent anti-TNF therapy50, further highlighting the relevance of membrane-bound TNF in IBD pathogenesis.
Current and emerging drugs
T-cell trafficking: integrin blockers and beyond. Studies over the past 10 years have found that ∼30–50% of patients with IBD do not respond to anti-TNF therapy, indicative of the need for new therapies. Experimental studies indicated that blockade of activated lymphocyte homing to the inflamed gut might provide a new approach for therapy of intestinal inflammation51,52. Subsequently, the anti-α4 integrin antibody natalizumab was tested in clinical trials for Crohn's disease therapy to block T-cell homing to the inflamed intestine via α4β7 integrins53,54,55 (Fig. 1). However, in spite of evidence for clinical efficacy in Crohn's disease, treatment-related JC virus infections causing progressive multifocal leukoencephalopathy limited the use of this agent in IBD therapy56. For example, in JC virus-seropositive patients with prior immunosuppressant use, the incidence of progressive multifocal leukoencephalopathy during months 25–48 of natalizumab therapy was reported to be 19.5 per thousand; without prior immunosuppressant use, the incidence during months 25–48 was ∼7.4 per thousand57. These infections were probably related to natalizumab-induced blockade of T-cell homing to the brain via α4β1 integrins, suggesting that a more specific blockade of α4β7 integrins was important. Subsequently, the α4β7-integrin-specific antibody vedolizumab was developed and showed efficacy in clinical phase III trials for remission induction and maintenance in Crohn's disease and ulcerative colitis58,59,60,61,62,63.
Although controlled clinical trials suggested that vedolizumab might induce more rapid clinical remission in ulcerative colitis than in Crohn's disease59,60, subsequent real-world data confirmed efficacy of this drug for moderate–severe Crohn's disease in routine clinical practice64 with similar rates of long-term remission in Crohn's disease and ulcerative colitis65. The reasons for potential differences between vedolizumab in Crohn's disease versus ulcerative colitis remain to be determined. Clinically, vedolizumab and TNF blockers are usually considered as alternative first-line induction treatment for patients with moderate–severe Crohn's disease and ulcerative colitis despite conventional therapy (with corticosteroids). Additionally, vedolizumab can be used in patients already exposed to anti-TNF agents. Prospective studies comparing vedolizumab with TNF blockers such as infliximab in anti-TNF-agent-naive patients will determine the precise positioning of vedolizumab in the treatment algorithm for IBD. On the basis of the success of the anti-α4β7 integrin approach with vedolizumab, further therapies targeting T-cell homing are currently tested in clinical trials including anti-MAdCAM1 antibodies (PF-00547659) and the anti-β7 integrin antibody etrolizumab66,67,68 (Fig. 1). The latter drug is particularly interesting, as it blocks not only α4β7-mediated homing but additionally T-cell retention via inhibition of αE(CD103)β7-mediated binding to E-cadherin on gut epithelial cells66,67. Consistently, in a humanized mouse model of colitis with ulcerative colitis T cells, etrolizumab was superior to vedolizumab in reducing T-cell trafficking in the inflamed tissue due to effects on ulcerative colitis T-cell retention66. However, phase III clinical data on clinical efficacy and safety of etrolizumab are still missing, although phase II data indicated efficacy for induction of remission in ulcerative colitis67.
Another important development in the context of immune cell trafficking in IBD relates to sphingosine 1-phosphate (S1P) signalling69. The bioactive lipid S1P has been shown to activate NF-κB and STAT3 transcription factors via a family of five G protein-coupled receptors (S1PR) expressed on lymphocytes (so-called inside-out signalling). Functionally, S1PR signalling induces cell proliferation, vascular permeability and angiogenesis69. Moreover, S1PR expressed in immune cells controls their egress from lymph nodes to lymph and plasma and S1PR agonists cause lymphopenia in blood and thoracic duct lymph by cell sequestration in lymph nodes69. Inhibition of lymphocyte recirculation via S1PR signalling suppressed experimental colitis and development of colitis-associated neoplasias in mice70,71,72. Thus, S1P receptor agonists (ozanimod (formerly known as RPC1063), APD334 and MT-1303) have been tested in human ulcerative colitis. For instance, ozanimod is an oral agonist of S1PR subtypes 1 and 5 that induces peripheral lymphocyte sequestration. A phase II trial indicated that ozanimod (daily dose of 1 mg) results in a slightly higher clinical remission rate in ulcerative colitis than placebo, suggesting that such drugs might be therapeutically effective in human ulcerative colitis73. However, further prospective studies are needed to determine efficacy and safety of ozanimod treatment in ulcerative colitis.
Emerging targets in fibrosis and tissue remodelling. Tissue remodelling and destruction in patients with IBD is controlled by MMPs. In this context, expression of MMP9 was found to be increased in IBD, particularly in patients with ulcerative colitis74. Functional data in experimental models of inflammation have suggested an important role of MMP9 in impairing colonic epithelial permeability and augmenting inflammation via activation of myosin light chain kinase (MLCK)74. Furthermore, MMP9 favoured angiogenesis and created a proteolytic environment in the inflamed gut of a mouse model of colitis that stimulated the influx of myeloid cells into the colonic epithelium and the production of TNF75,76. Consecutively, a potent and highly selective allosteric MMP9 inhibitor (humanized monoclonal antibody GS-5745) has been developed and is currently being tested in clinical trials in patients with IBD76 (Fig. 2). However, in September 2016, the company has stopped its combined phase II/III clinical study of GS-5745 among patients with moderately to severely active ulcerative colitis due to insufficient evidence of a treatment benefit in the group of patients randomly assigned to receive either one of two doses of GS-5745 (Ref. 77).
To ameliorate tissue fibrosis in IBD, enzymes controlling degradation of matrix compounds might be druggable targets. Specifically, a study has examined carbohydrate sulfotransferase 15 (CHST15) in gut inflammation78. CHST15 is a specific enzyme biosynthesizing chondroitin sulfate E that binds to various pathogenic mediators and favours tissue fibrosis. In experimental acute dextran sulfate sodium colitis, small-interfering RNA (siRNA)-based silencing of CHST15 reduced colitis activity and intestinal accumulation of F4/80+ macrophages and ER-TR7+ fibroblasts. In chronic dextran sulfate sodium colitis, CHST15 siRNA reduced colitis activity and numbers of α-SMA (smooth muscle actin)-positive fibroblasts and collagen deposition. Furthermore, a phase I study in 18 patients with Crohn's disease published in 2016 determined the safety of STNM01, a synthetic double-stranded RNA oligonucleotide directed against CHST15, in Crohn's disease79. The majority of individuals who received STNM01 showed a reduction of endoscopic inflammation as compared with placebo therapy. Moreover, histological analyses revealed that STNM01 reduces tissue fibrosis in Crohn's disease. Larger prospective studies on this compound are needed to determine the efficacy of this new therapeutic approach.
New blockers of proinflammatory cytokines and cytokine signalling. On the basis of the success of anti-TNF agents in IBD there has been an intensive search for additional effective anticytokine strategies. However, several studies on new cytokine blockers have yielded disappointing results. For instance, the anti-IFNγ antibody fontolizumab showed low efficacy in patients for treatment of active Crohn's disease80. Moreover, the anti-IL-17A antibody secukinumab resulted in aggravation of Crohn's disease in many patients, possibly owing to the protective effects of IL-17A on gut epithelial cells81,82,83. Consistently, IL-17A inactivation did not result in amelioration of experimental colitis in mice84,85. In addition to IFNγ and IL-17A blockers, two prospective studies did not show efficacy of anti-IL-13 antibodies (anrukinzumab, tralokinumab) in patients with ulcerative colitis despite promising results in animal models of colitis86,87,88,89. In contrast to these observations, additional cytokine blockers have shown more promising results in clinical trials that will be reviewed in the next paragraphs (Figs 3,4).
IL-6 is a proinflammatory cytokine activating immune cells90,91. In patients with IBD, levels of IL-6 and its agonistic soluble receptor (sIL-6R) are induced and mediate activation of T cells and their resistance against programmed cell death (apoptosis)92. In experimental colitis models, IL-6R blockade was effective in suppressing intestinal inflammation. Consistently, a small pilot study using an anti-IL-6R antibody (tocilizumab, previously known as MRA) suggested higher response and remission rates in Crohn's disease than the placebo group93. Additionally, according to results presented in abstract form, an IL-6 antibody (PF-04236921) yielded higher clinical response (Crohn's disease activity index-70) and remission rates in patients with Crohn's disease than placebo therapy94. However, cases with abscess formation and perforations were noted upon start of therapy possibly owing to protective, proliferative effects of membrane-bound IL-6R signalling on gut epithelial cells. In future studies, gp130–Fc fusion proteins could elucidate the role of sIL-6R signalling in Crohn's disease, as such proteins specifically block signalling via the soluble but not the membrane-bound IL-6R.
IL-12 p35–p40 and IL-23 p19–p40 are two heterodimeric, proinflammatory cytokines that are induced in the inflamed mucosa of patients with Crohn's disease95,96. Consistent with the type 1 T helper (TH1)-inducing potential of IL-12, Crohn's disease was found to be associated with mucosal TH1 responses. Moreover, type 17 T helper (TH17) responses were noted in both patients with Crohn's disease and ulcerative colitis39,97, possibly owing to the presence of IL-23 as a well-known activator of TH17 T cells. These data provided a rational basis for targeting of TH1 and TH17 cytokines in IBD (Fig. 2). Functional studies with genetically engineered animals and IL-23 p19 and p40 blockers suggested that blockade of these cytokine subunits might effectively suppress intestinal inflammation in mouse models of colitis98,99,100,101,102,103,104. In particular, IL-23 inhibition was effective and prevented activation of T cells and innate lymphoid cells and tissue destruction in vivo.
Subsequently, various antibodies against IL-12–IL-23 p40 and IL-23 p19 subunits were developed for clinical trials (such as ABT-874, ustekinumab, risankizumab, LY-2525623, AMG139/MEDI2079 and guselkumab)105,106,107. Studies with ABT-874 and ustekinumab as p40 blockers demonstrated higher response rates in patients with Crohn's disease than placebo. Initial studies also revealed that ustekinumab was particularly effective for therapy in patients with Crohn's disease who had previously taken anti-TNF agents105,106. On the basis of successful phase III studies in both anti-TNF agent-naive and anti-TNF agent-experienced patients (UNITI-1 and UNITI-2 programmes), ustekinumab was recently approved for Crohn's disease therapy in the USA and in Europe)108. Potentially, p19 blockers such as risankizumab will also be available for Crohn's disease therapy in the future, as the latest phase II data presented as a late breaker abstract suggested efficacy for this antibody in patients with active Crohn's disease109.
Cytokine signalling is mediated upon binding of cytokines to their specific receptors via intracellular activation of Janus kinases (JAKs: JAK1, JAK2, JAK3, TYK2). Thus, blockade of JAK kinases might be used to suppress cytokine signalling in mucosal immune cells. As individual JAKs mediate cell activation via several cytokines (for example, JAK3 is activated via IL-2, IL-4, IL-7, IL-9, IL-15 and IL-21) with proposed proinflammatory roles in colitis110,111,112,113, this approach opens the possibility to block the activity of several proinflammatory cytokines simultaneously. Indeed, several JAK inhibitors (tofacitinib, ABT494 and filgotinib) have been developed for clinical therapy114,115. Interestingly, the JAK1–JAK3 blocker tofacitinib, a suppressor of T-cell, natural-killer-cell and B-cell activation, yielded very promising results in a phase II study in patients with ulcerative colitis, but was not effective in patients with Crohn's disease114,115. Moreover, filgotinib, a selective JAK1 inhibitor, showed increased remission rates in patients with moderate to severe Crohn's disease116. Although the efficacy and safety profiles of these drugs will have to be determined in large phase III trials, these findings indicate that JAK inhibitors hold promise for clinical therapy of patients with IBD.
Finally, phosphodiesterase (PDE)4 inhibitors are currently being tested in patients with IBD. PDE4 inhibitors such as apremilast and roflumilast regulate inflammatory processes by degrading cyclic adenosine 3′5′-monophosphate (cAMP), a key second messenger117. Inhibition of PDE4 increases the intracellular cAMP level, which in turn blocks proinflammatory mediators and favours production of anti-inflammatory proteins. In particular, apremilast has been found to impair the production of the proinflammatory cytokines IFNγ, TNF, IL-12, IL-17 and IL-23 (Ref. 118), indicating that PDE4 blockers are multicytokine inhibitors with potential therapeutic effects in IBD.
Blockers of transcription factors controlling cytokine gene transcription. Transcription factors regulating cytokine gene expression are potential future drug targets in IBD119,120. Theoretically, targeting such regulatory proteins might enable suppression of the production of several proinflammatory cytokines at the same time. Potential strategies for targeting include siRNA, DNAzymes and chemical inhibitors. A study published in 2016 used a chemical inhibitor of RORγt, a master transcription factor in TH17 cells, for successful therapy of experimental T-cell-dependent colitis in mice120. Furthermore, genetic RORγ deficiency of T cells prevented T-cell transfer of colitis in RAG-knockout mice84. As RORA and RORC proteins, as well as TH17 cytokines, are augmented in patients with IBD121,122, these data suggested that targeting of ROR proteins might be useful in these patients. Moreover, both genetic and pharmacological (via DNAzyme) blockade of GATA3, a key transcription factor for TH2 cytokine gene transcription, ameliorated chronic oxazolone-mediated and TNBS (2,4,6-trinitrobenzenesulfonic acid)-mediated colitis in mice119. As GATA3 expression is induced in patients with active ulcerative colitis and correlates with TH2 and TH9 cytokine levels in this disease, these observations indicate that GATA3 might be targeted for therapy of ulcerative colitis in humans. Indeed, GATA3 DNAzyme therapy has been successfully tested in patients with asthma123, a chronic inflammatory disorder of the airways associated with type 2 T helper (TH2) cytokine production.
Strengthening barrier function and activation of anti-inflammatory pathways. Escherichia coli Nissle (EcN) is a nonpathogenic Gram-negative strain that controls intestinal barrier function and induces anti-inflammatory proteins124,125. EcN is an established clinical therapy for patients with ulcerative colitis and exhibits similar anti-inflammatory effects compared with 5-ASAs125. EcN has direct antimicrobial effects, controls biofilm formation, stimulates human β-defensin production by intestinal epithelial cells, and strengthens tight junctions by upregulating zonula occludens proteins125. In addition to this probiotic strain, several other probiotic approaches as well as faecal transplantation have been considered for IBD therapy, although unequivocal results have been obtained126,127. However, a randomized controlled trial in adults with active ulcerative colitis demonstrated that faecal microbiota transplantation (50 ml, via enema from healthy anonymous donors) once weekly for 6 weeks induced markedly higher remission rates than placebo126. Further studies are required to determine the efficacy and safety of this approach in larger patient cohorts and over longer time periods.
Additional therapeutic approaches for IBD have been designed that might regulate barrier function and anti-inflammatory pathways. Defects in mucin production are well-known in patients with ulcerative colitis128, and so phosphatidylcholine (lecithin) therapy has been tested in patients with promising results in phase II studies129. The results of the phase III study in patients with ulcerative colitis are expected in 2017. Moreover, IL-22 therapy or modulation of IL-22-binding protein have been tested successfully in mouse colitis models and proposed as new approaches for IBD therapy130. The IL-22 cytokine directly activates proliferation of intestinal epithelial cells via STAT3 activation and induces production of protective barrier proteins such as REG proteins131. Moreover, modulators of Toll-like receptor (TLR) signalling have been considered for IBD therapy132. CpG-site-containing oligonucleotides suppress immune cell activation and protect barrier function in experimental colitis via TLR9 signalling133. Finally, the TLR7 ligand imiquimod suppressed CD11c+ dendritic cells and activated intestinal epithelial cells to produce antimicrobial peptides, resulting in reduced colitis activity134.
The ratio between effector T cells and regulatory T (Treg) cells is markedly increased in patients with IBD135. Thus, it is tempting to speculate that increasing Treg-cell numbers via Treg-cell transfer might restore the balance between proinflammatory and anti-inflammatory immune cells as a new therapeutic approach in IBD. Indeed, naturally occurring Treg cells, TGFβ-induced Treg cells as well as ex vivo expanded Treg cells have been used for therapy of experimental colitis in mice and led to suppressed colitis activity induced by effector T cells136,137. In patients with IBD, a 12-week, single-injection, escalating-dose, phase I/IIa clinical pilot study in refractory Crohn's disease with ovalbumin-specific Treg cells was well tolerated and had dose-related efficacy138 (Fig. 3). On the basis of these results, various clinical studies are currently studying the effects of Treg-cell based immune therapy in IBD.
Finally, activation of TGFβ signalling in immune cells via inhibition of SMAD7 has been tested in a phase II study in patients with Crohn's disease139,140. This study was based on previous findings showing that blockade of SMAD7 expression in experimental colitis augmented TGFβ signalling via SMAD3 and caused suppression of colitis activity. The clinical phase II trial with an antisense SMAD7 blocker, denoted mongersen, showed markedly higher rates of remission and clinical response in mongersen-treated patients than the placebo-treated group. Owing to these promising results of the phase II programme, a phase III study will determine the efficacy and safety of mongersen in a larger group of patients with Crohn's disease.
Stem cells for Crohn's disease fistulas. Crohn's disease is associated with the development of complex fistulas that are challenging to treat141,142. Adipose-derived allogeneic stem cells have been considered as new treatment approaches for such fistulas142,143. Experimental studies revealed that mesenchymal stem cells (MSCs) might exert potent immunomodulatory effects on antigen-specific T cells in Crohn's disease through paracrine and cell–cell contact-mediated actions144. Clinically, local administration of allogeneic, expanded MSCs in initial trials was not associated with severe adverse events in patients with Crohn's disease who had perianal fistulas and seemed to promote healing. A large randomized trial subsequently showed that allogeneic MSCs (120 million Cx601 cells) induced remission (closure of external openings of fistulas and absence of collections >2 cm) more frequently than placebo145. Furthermore, a phase I–IIa study suggested potential beneficial effects of MSCs in rectovaginal fistulas in Crohn's disease, suggesting that MSCs might be broadly applicable for fistula therapy in patients with Crohn's disease146.
Several new drugs such as anti-TNF agents and vedolizumab have been introduced into clinical IBD therapy in the past few decades that have helped to reduce corticosteroid use and to augment response and remission rates. Evidence in both Crohn's disease and ulcerative colitis has been obtained that indicate some of these drugs synergistically suppress immune cell activation and gut inflammation (for example, azathioprine plus infliximab), highlighting the potential of combination therapies14,35. However, there is still a large unmet need for novel therapeutic approaches as many patients do not respond to the clinically approved drugs, including TNF blockers and vedolizumab14,28,60. Thus, a plethora of new drugs are currently being tested in clinical trials in IBD that challenge established treatment regimens (Fig. 2). Many of these new therapeutic approaches have been developed on the basis of studies in IBD mouse models, genetic studies, analyses of IBD tissues and new insights into inflammatory pathways in other chronic inflammatory disorders, such as rheumatoid arthritis and psoriasis97,117,147,148. Some of these new agents might gain approval by FDA and the European Medicines Agency and might enable new strict end points in IBD therapy to be achieved149,150, including mucosal healing on endoscopy, deep remission (clinical remission plus mucosal healing), transmural healing and histological healing, thereby raising the bar for future drugs in IBD therapy and possibly preventing severe IBD-associated complications such as surgery and hospitalizations. In this context, new cytokine and signalling blockers have yielded promising results and will probably add to our future clinical armamentarium in patients with IBD106,115. With the introduction of additional approved drugs in the future, it will be of crucial importance to identify biomarkers to predict and monitor therapeutical success to enable individualized therapy in IBD.
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M.F.N. has served as an adviser for Abbvie, Boehringer, Genentech, Giuliani/PPM, Janssen, MSD, Pentax and Takeda.
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Neurath, M. Current and emerging therapeutic targets for IBD. Nat Rev Gastroenterol Hepatol 14, 269–278 (2017). https://doi.org/10.1038/nrgastro.2016.208
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