What is it about?
Secukinumab, an interleukin-17A (IL-17A) antagonist, is the first non-TNF alpha inhibitor agent licensed for ankylosing spondylitis (AS), which opens up a new era of alternative cytokine targets beyond TNF. Areas covered: This review explores the pathophysiology and scientific evidence behind the use of this new mode of action and discusses the basis for its efficacy and clinical utility in the management of AS. In particular, how the emergent data points towards the efficacy of secukinumab and ixekizumab, a second emergent IL-17A blocker, in AS has helped focus research into the IL-23/17 axis in entheseal driven disease in man and how IL-17A inhibition may be linked to the presence of innate and adaptive immune cell populations capable of IL-17A elaboration in these target tissues. Expert commentary: Collectively these emergent data point towards an efficacious role of IL-17A inhibition strategies targeting AS pathogenesis in a fundamental way whilst carrying a good safety profile.
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Why is it important?
The IL-17A blockers have provided an alternative mode of action for biologic treatment in AS. But which is more suited to your patient TNFi or IL-17A blockade? This paper will layout the risks and benefits of IL-17A inhibitors in AS and its extra-articular manifestations.
Perspectives
Ixekizumab and secukinumab have good clinic trial data in AS.
Sayam Dubash
University of Leeds
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This page is a summary of: The advent of IL-17A blockade in ankylosing spondylitis: secukinumab, ixekizumab and beyond, Expert Review of Clinical Immunology, January 2019, Taylor & Francis,
DOI: 10.1080/1744666x.2019.1561281.
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