Ixekizumab: an anti-IL-17A monoclonal antibody for the treatment of psoriatic arthritis

被引:27
作者
Toussirot, Eric [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Hosp Besancon, INSERM, CIC 1431, Clin Invest Ctr Biotherapy, F-25000 Besancon, France
[2] Univ Hosp Besancon, Federat Hosp Univ INCREASE, Besancon, France
[3] Univ Hosp Besancon, Dept Rheumatol, Besancon, France
[4] Univ Bourgogne Franche Comte, Dept Therapeut, Besancon, France
[5] Univ Bourgogne Franche Comte, EPILAB Epigenet Infect Virales & Malad Inflammato, Besancon, France
关键词
IL-17A; IL-23/Th17; pathway; psoriatic arthritis; ixekizumab; DISEASE-ACTIVITY; DOUBLE-BLIND; MAST-CELLS; T-CELLS; TH17; INTERLEUKIN-17; SECUKINUMAB; RECEPTOR; PATHWAYS; IL-17;
D O I
10.1080/14712598.2018.1410133
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Psoriatic arthritis (PsA) is an inflammatory rheumatic disease that manifests itself with synovitis, dactylitis, enthesitis and also axial involvement. Interleukin-17A has been identified as a master cytokine in the inflammatory response and pathogenesis of PsA and spondyloarthritis in general. Ixekizumab is a new humanized monoclonal antibody that blocks the biological activity of IL-17A. This biological agent has previously demonstrated a high level of efficacy in psoriasis. Areas covered: This review discusses the basic immunology of the IL-17 cytokine family, the contribution of IL-17A to the immunopathogenesis of PsA, the clinical trials that evaluated ixekizumab in patients with PsA (SPIRIT program) and the safety of this agent. Expert opinion: Ixekizumab demonstrated its efficacy in different aspects of PsA including peripheral joint involvement, dactylitis, skin symptoms and patient reported outcomes in the 2 phase III trials from the SPIRIT program. Its safety profile was consistent with previous observations in patients with psoriasis. The role of IL-17A in the management of patients with PsA needs further clarification. According to EULAR recommendations for the management of PsA, IL-17A inhibitors may be used as second line biological DMARDs after TNF inhibitors.
引用
收藏
页码:101 / 107
页数:7
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