2018
DOI: 10.3748/wjg.v24.i23.2457
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Vedolizumab for inflammatory bowel disease: From randomized controlled trials to real-life evidence

Abstract: The biologic antitumor necrosis factor alpha (anti-TNFα) agents have revolutionised the treatment of inflammatory bowel disease (IBD). However, some patients experience primary nonresponse, loss of response, or intolerance. Therefore, introducing a newer class of therapy with a mechanism of action that acts on different inflammatory pathways involved in IBD pathogenesis is appealing. Vedolizumab is a fully humanised monoclonal antibody that selectively targets α4β7 integrin. Based on the results of the pivotal… Show more

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Cited by 73 publications
(61 citation statements)
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“…Via selective inhibition of the interaction between α4β7 integrin and mucosal addressin cell adhesion molecule-1 (MAdCAM-1), vedolizumab inhibits the leukocyte binding to endothelial surface and its extravasation into inflamed GI parenchymal tissue. Both of these new therapeutic options appear to be associated with rapid and sustained clinical effect, paralleled by a favorable safety profile, dampening of the inflammatory cascade, and lack of immunogenicity (26)(27). The recovery of skin lesions in MCD is variable and does not parallel that of intestinal lesions.…”
Section: Discussionmentioning
confidence: 99%
“…Via selective inhibition of the interaction between α4β7 integrin and mucosal addressin cell adhesion molecule-1 (MAdCAM-1), vedolizumab inhibits the leukocyte binding to endothelial surface and its extravasation into inflamed GI parenchymal tissue. Both of these new therapeutic options appear to be associated with rapid and sustained clinical effect, paralleled by a favorable safety profile, dampening of the inflammatory cascade, and lack of immunogenicity (26)(27). The recovery of skin lesions in MCD is variable and does not parallel that of intestinal lesions.…”
Section: Discussionmentioning
confidence: 99%
“…In contrast to other anti-adhesion drugs, the use of vedolizumab in UC patients did not increase the rates of opportunistic or enteric infections and there were no reported cases of progressive multifocal leukoencephalopathy [53]. Following encouraging results in randomized, double-blind, placebo-controlled trials in the pivotal phase III GEMINI studies, vedolizumab has been approved by US FDA for the treatment of adult patients with active UC who had a poor response to standard therapies [54]. Nevertheless, mononuclear phagocyte enrichment was detected in non-responder UC patients before vedolizumab treatment, which further increased post treatment [52], partly explaining why some UC patients do not respond as well to this drug.…”
Section: The Role Of Biomarkers and Treatment Options In Ucmentioning
confidence: 99%
“…In addition, drug treatments with a mechanism of action similar to that of blood cell apheresis have emerged. Vedolizumab, a mAb that targets a4b7 integrins, exerting in a gut-selective mechanism of action, has emerged for the induction of remission in active IBD patients [44]. Based on clinical trials and actual clinical data, vedolizumab is expected to be effective in treating patients who are resistant to anti-TNF-a antibody treatment [45].…”
Section: Ibd Treatment From the Perspective Of The Adaptive Immune Symentioning
confidence: 99%