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Rheumatology (Oxford). 2016 Dec;55(suppl 2):ii43-ii55.

Effect of IL-17 receptor A blockade with brodalumab in inflammatory diseases.

Author information

1
Amgen, Thousand Oaks, CA anirula@me.com.
2
Amgen, Thousand Oaks, CA.
3
Amgen, Seattle, WA, USA.

Abstract

IL-17 cytokines are expressed by a variety of cells and mediate host defence against extracellular pathogens. IL-17 is upregulated at sites of inflammation and can synergize with other cytokines, such as TNF-α, to amplify the inflammatory response. Activation of these signalling pathways has been hypothesized to contribute to the underlying pathogenesis of several inflammatory diseases, including psoriasis, RA, PsA and asthma. Thus the IL-17 signalling pathway is an attractive target for the development of therapeutic agents to modulate aberrant inflammatory responses. This review of the clinical development of therapeutic agents that target IL-17 signalling pathways in inflammatory diseases focuses on brodalumab, a human anti-IL-17 receptor A mAb. The cumulative findings of early clinical studies with anti-IL-17 agents, including brodalumab, secukinumab and ixekizumab, provide strong evidence for the role of IL-17 signalling in the pathophysiology of certain inflammatory diseases and support the potential use of these agents in treating these diseases.

KEYWORDS:

Crohn’s disease; asthma; brodalumab; interleukin-17; psoriasis; psoriatic arthritis; rheumatoid arthritis

PMID:
27856660
DOI:
10.1093/rheumatology/kew346
[Indexed for MEDLINE]

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