IL-4 and IL-13 Inhibition in Atopic Dermatitis

被引:1
|
作者
Matsunaga, Matthew C. [1 ]
Yamauchi, Paul S. [2 ,3 ,4 ]
机构
[1] Univ Minnesota, Sch Med, Minneapolis, MN 55455 USA
[2] Inst Dermatol, Santa Monica, CA 90404 USA
[3] Skin Care Ctr, Santa Monica, CA 90404 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
关键词
CYTOKINE GENE-CLUSTER; DERMAL FIBROBLASTS; BLOOD EOSINOPHILS; SIGNAL TRANSDUCER; STRATUM-CORNEUM; TRANSGENIC MICE; INTERLEUKIN-4; PREVALENCE; ECZEMA; CELLS;
D O I
暂无
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Atopic dermatitis (AD) is a chronic, prevalent, multi-factorial condition that affects infants, children, and adults. Beyond topical therapy, a variety of systemic agents such as steroids, methotrexate, cyclosporine, azathioprine, mycophenoloic acid, and other agents are utilized to treat moderate to severe AD. However, these agents are associated with potential long term adverse events 'and organ toxicity. There is an unmet need for a safer, long-term systemic agent to adequately control moderate to severe AD. The role of the Th2 cytokines, IL-4 and IL-13, in AD has led to the development of biologic agents to treat AD. The aim of this article is to review the role of IL-4 and 11,13 in the pathogenesis of AD and discuss some of the clinical trial data that target and inhibit IL-4 and IL-13 in positively altering the course and outcome of AD.
引用
收藏
页码:925 / 929
页数:5
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