乌斯特基努马
医学
免疫学
白细胞介素23
银屑病
细胞因子
银屑病性关节炎
免疫系统
炎症
促炎细胞因子
白细胞介素
肿瘤坏死因子α
阿达木单抗
作者
Michele W.L. Teng,Edward P. Bowman,Joshua McElwee,Mark J. Smyth,Jean‐Laurent Casanova,Andrea M. Cooper,J. Daniel
出处
期刊:Nature Medicine
[Springer Nature]
日期:2015-06-29
卷期号:21 (7): 719-729
被引量:749
摘要
The cytokine interleukin-12 (IL-12) was thought to have a central role in T cell-mediated responses in inflammation for more than a decade after it was first identified. Discovery of the cytokine IL-23, which shares a common p40 subunit with IL-12, prompted efforts to clarify the relative contribution of these two cytokines in immune regulation. Ustekinumab, a therapeutic agent targeting both cytokines, was recently approved to treat psoriasis and psoriatic arthritis, and related agents are in clinical testing for a variety of inflammatory disorders. Here we discuss the therapeutic rationale for targeting these cytokines, the unintended consequences for host defense and tumor surveillance and potential ways in which these therapies can be applied to treat additional immune disorders.
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