Emerging treatments for inflammatory bowel disease
- PMID: 32076497
- PMCID: PMC7003169
- DOI: 10.1177/2040622319899297
Emerging treatments for inflammatory bowel disease
Abstract
Inflammatory bowel disease (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), is characterized by chronic inflammation, a relapsing and remitting clinical course, requirement for lifelong medication and often, significant morbidity. While multiple effective therapeutic options exist for the treatment of IBD, a proportion of patients will either fail to respond or lose response to therapy. Advances in therapeutics, such as the gut-specific anti-integrins, now offer patients an alternative option to systemic immunosuppression. Anti-interleukin 12 (anti-IL-12)/IL-23 agents offer new and effective treatment options for CD, while the oral small molecules now offer an oral alternative for the treatment of moderate-to-severe disease, previously requiring subcutaneous injection or intravenous infusion. Alternatives to pharmacological treatment such as stem-cell transplant and faecal microbiota transplant are also showing some promise in the treatment of both CD and UC.
Keywords: Crohn’s disease; inflammatory bowel disease; ulcerative colitis.
© The Author(s), 2020.
Conflict of interest statement
Conflict of interest statement: AOC has received speaker and advisory board fees from MSD Human Health, Abbvie, Takeda and Janssen Pharmaceuticals.
Figures
References
-
- Harris M, Hartman D, Lemos B, et al. AVX-470, an orally delivered anti-tumour necrosis factor antibody for treatment of active ulcerative colitis: results of a first-in-human trial. J Crohn’s Colitis 2016; 10: 631–640. - PubMed
-
- Berlin C, Berg E, Briskin M. α4β7 integrin mediates lymphocyte bindings to the mucosal vascular addressin MAdCAM–1. Cell 1993; 74: 185–195. - PubMed
-
- Vermiere S, O’Byrne S, Keir M, et al. Etrolizumab as induction therapy for ulcerative colitis: a randomized, controlled, phase 2 trial. Lancet 2014; 384: 309–318. - PubMed
Publication types
LinkOut - more resources
Full Text Sources
Other Literature Sources
