The role of IL-17 in psoriasis

被引:62
|
作者
Malakouti, Mona [1 ,2 ]
Brown, Gabrielle Elena [2 ,3 ]
Wang, Eva [2 ,4 ]
Koo, John [2 ]
Levin, Ethan C. [2 ]
机构
[1] Rosalind Franklin Univ Med & Sci, Chicago Med Sch, N Chicago, IL USA
[2] Univ Calif San Francisco, Dept Dermatol, Psoriasis & Skin Treatment Ctr, San Francisco, CA 94118 USA
[3] Univ Arizona, Coll Med, Tucson, AZ USA
[4] Univ S Alabama, Sch Med, Mobile, AL 36688 USA
关键词
Biologics; brodalumab; Ixekizumab; secukinumab; Th17; DELTA T-CELLS; SEVERE PLAQUE PSORIASIS; HETERODIMERIC CYTOKINE; INFLAMMATORY DISEASES; SKIN INFLAMMATION; CUTTING EDGE; DOUBLE-BLIND; TH17; CELLS; INTERLEUKIN-17; RECEPTOR;
D O I
10.3109/09546634.2013.879093
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Psoriasis is a chronic skin condition traditionally believed to involve the Th1 pathway. Recently, the IL-23/Th17/IL-17 pathway has been highlighted in the pathogenesis of psoriasis and other autoimmune inflammatory conditions. From a clinician's perspective, we sought to review the basic science data relevant to IL-17's role in psoriasis pathogenesis. Methods: We performed a Pubmed and Web of Knowledge search for English articles starting from 1990 that discussed the Th17 pathway. Search terms such as "IL-17'' and "psoriasis'' were utilized. Results: The IL-17 pathway is regulated by IL-23, a cytokine that is vital for the expansion and maintenance of the Th17 cell population. Th17 derived cytokines (IL-17A, IL-17F, IL-17A/F and IL-22) were elevated in both psoriasis-like murine models and human psoriatic lesional biopsies. Ixekizumab (anti-IL-17A) treatment of psoriasis was found to normalize levels of IL-17 downstream gene products. Conclusion: Both preclinical and clinical studies support the central role of IL-17 in the pathogenesis of psoriasis.
引用
收藏
页码:41 / 44
页数:4
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