Lichnog C, Klabunde S, Becker E, Fuh F, Tripal P, Atreya R, Klenske E, Erickson R, Chiu H, Reed C, Chung S, Neufert C, Atreya I, Mcbride J, Neurath M, Zundler S (2019)
Publication Type: Journal article
Publication year: 2019
Book Volume: 10
Article Number: 39
Background: Anti-integrin therapy is a new frontline strategy in the treatment of inflammatory bowel diseases (IBD). The anti-beta 7 integrin antibody etrolizumab is currently being investigated for safety and efficacy in Crohn's disease (CD) and ulcerative colitis (UC) in several phase III trials. Mechanistically, etrolizumab is known to block beta 7 integrin ligand binding and reduces intestinal trafficking of beta 7-expressing cells. Etrolizumab blocks beta 7 integrin ligand binding and reduces beta 7-positive lymphocyte migration and retention in the inflamed gut mucosa, but the exact mechanisms by which this inhibition occurs are not fully understood.
APA:
Lichnog, C., Klabunde, S., Becker, E., Fuh, F., Tripal, P., Atreya, R.,... Zundler, S. (2019). Cellular Mechanisms of Etrolizumab Treatment in Inflammatory Bowel Disease. Frontiers in Pharmacology, 10. https://doi.org/10.3389/fphar.2019.00039
MLA:
Lichnog, Charlotte, et al. "Cellular Mechanisms of Etrolizumab Treatment in Inflammatory Bowel Disease." Frontiers in Pharmacology 10 (2019).
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