| Literature DB >> 32719044 |
Marine Fauny1, David Moulin2, Ferdinando D'Amico3,4, Patrick Netter2, Nadine Petitpain5, Djesia Arnone4, Jean-Yves Jouzeau2, Damien Loeuille1,2, Laurent Peyrin-Biroulet6.
Abstract
Secukinumab, ixekizumab and brodalumab are monoclonal antibody therapies that inhibit interleukin (IL)-17 activity and are widely used for the treatment of psoriasis, psoriatic arthritis and ankylosing spondylitis. The promising efficacy results in dermatology and rheumatology prompted the evaluation of these drugs in Crohn's disease and ulcerative colitis, but the onset of paradoxical events (disease exacerbation after treatment with a theoretically curative drug) prevented their approval in patients with inflammatory bowel diseases (IBDs). To date, the pathophysiological mechanisms underlying these paradoxical effects are not well defined, and there are no clear guidelines for the management of patients with disease flare or new IBD onset after anti-IL-17 drug therapy. In this review, we summarise the literature on putative mechanisms, the clinical digestive effects after therapy with IL-17 inhibitors and provide guidance for the management of these paradoxical effects in clinical practice. © Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: arthritis, psoriatic; biological therapy; spondylitis, ankylosing
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Year: 2020 PMID: 32719044 DOI: 10.1136/annrheumdis-2020-217927
Source DB: PubMed Journal: Ann Rheum Dis ISSN: 0003-4967 Impact factor: 19.103