Therapeutic Targeting of IL-17 and IL-23 Cytokines in Immune-Mediated Diseases

被引:147
|
作者
Fragoulis, George E. [1 ]
Siebert, Stefan [1 ]
McInnes, Iain B. [1 ]
机构
[1] Univ Glasgow, Inst Infect Immun & Inflammat, Glasgow G12 8QQ, Lanark, Scotland
来源
关键词
interleukin-17; interleukin-23; IL-23/IL-17; axis; psoriasis; psoriatic arthritis; INTERLEUKIN-12/23; MONOCLONAL-ANTIBODY; TO-SEVERE PSORIASIS; QUALITY-OF-LIFE; SEVERE PLAQUE PSORIASIS; EARLY CLINICAL-RESPONSE; CONTROLLED PHASE-II; DOUBLE-BLIND; RHEUMATOID-ARTHRITIS; CONTROLLED-TRIAL; OPEN-LABEL;
D O I
10.1146/annurev-med-051914-021944
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The discovery of the biological functions of the interleukin-23/-17 axis led to the identification of IL-23 and IL-17 as important participants in the pathogenesis of several immune-mediated diseases. Therapeutic agents targeting these cytokines and/or their receptors have now been developed as potential treatment strategies for common immune-mediated diseases. Anti-IL-17 and anti-IL-12/-23 regimens appear particularly effective in psoriasis, with promising results in spondyloarthropathies also emerging. Overall, these agents appear well tolerated, with adverse-event rates that are commensurate with those in other biologic treatment programs. The strategic utility of these new agents, however, remains uncertain, and further studies will be required to determine their place in the context of existing conventional and biologic immune-modifying agents.
引用
收藏
页码:337 / 353
页数:17
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