Emerging Immunomodulatory Therapies and New Treatment Paradigms for Axial Spondyloarthritis

被引:13
作者
Mease, Philip [1 ]
机构
[1] Univ Washington, Sch Med, Rheumatol Res, Swedish Med Ctr,Providence St Joseph Hlth, 601 Broadway Suite 600, Seattle, WA 98122 USA
关键词
Axial spondyloarthritis; Ankylosing spondylitis; Non-radiographic axial spondyloarthritis; Biologic therapy; TNF inhibitor; IL-17; inhibitor; SOCIETY CLASSIFICATION CRITERIA; ANKYLOSING-SPONDYLITIS; PSORIATIC-ARTHRITIS; OPEN-LABEL; INTERLEUKIN-17; RECOMMENDATIONS; INFLAMMATION; INHIBITOR; ENTHESIS; CELLS;
D O I
10.1007/s11926-019-0830-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of ReviewThe purpose of this review is to educate the reader about the evolving classification of axial spondyloarthritis (AxSpA) and describe recent treatment data from clinical trials of medications with mechanisms of action other than TNF inhibition. The review will also address emerging treatment strategies for AxSpA.Recent FindingsNew and more sensitive classification schema for AxSpA find that the prevalence of the disease is more than twice that of the historic definition of ankylosing spondylitis (AS), when patients without radiographically observable damage to the sacroiliac joints are included. TNF inhibitors have shown efficacy in the full spectrum of disease. IL-17 inhibitors, e.g., secukinumab and ixekizumab and janus kinase (JAK) inhibitors, have shown good efficacy and relatively good safety in radiographically defined AxSpA and are being tested in non-radiographic (nr) AxSpA. Several immunomodulatory medicines approved for psoriasis, psoriatic arthritis, and rheumatoid arthritis have not shown efficacy in AxSpA, highlighting the importance of conducting good-quality, placebo-controlled trials in this condition. Treatment strategies such as treat to target and tapering therapy are being studied.SummaryThere remains a large unmet need to identify and adequately treat the full spectrum of AxSpA. The use of TNF inhibitors has improved our ability to achieve remission or low disease activity in AxSpA. Newer medicines with different mechanisms of action, e.g., IL-17 or JAK inhibition, are also showing similar ability. Continued research, including identification of new targets of treatment, is critical.
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页数:7
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