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靶向治疗银屑病中的白细胞介素-22。

Targeting interleukin-22 in psoriasis.

机构信息

Department of Oncology, The Fist Affiliated Hospital of Anhui Medical University, 218 Jixi Road, Hefei, Anhui, 230022, China,

出版信息

Inflammation. 2014 Feb;37(1):94-9. doi: 10.1007/s10753-013-9715-y.

Abstract

Interleukin-22 (IL-22) is an IL-10 family cytokine that was recently discovered to be released by T helper 17 (Th17) cells, Th22 cells, etc. Recently, there is emerging evidence that IL-22 is involved in the development and pathogenesis of psoriasis. For instance, IL-22 can inhibit keratinocyte terminal differentiation and can induce psoriasis-like epidermis alterations; serum IL-22 levels were correlated with the disease severity of psoriasis patients, and IL-22 mRNA was positively expressed in the psoriatic skin lesions, but negatively expressed in the normal controls. All these findings suggest that IL-22 may be implicated in psoriasis; therapeutics targeting IL-22 may have promise as a potential therapeutic target for treating psoriasis. In the present review, we summarize recent advances on the role of IL-22 in the pathogenesis and treatment of psoriasis.

摘要

白细胞介素-22(IL-22)是一种白细胞介素 10 家族细胞因子,最近发现其由辅助性 T 细胞 17(Th17)细胞、Th22 细胞等释放。最近有研究表明,IL-22 参与了银屑病的发展和发病机制。例如,IL-22 可以抑制角质形成细胞的终末分化,并可诱导银屑病样表皮改变;血清 IL-22 水平与银屑病患者的疾病严重程度相关,且 IL-22mRNA 在银屑病皮损中呈阳性表达,而在正常对照中呈阴性表达。所有这些发现表明,IL-22 可能与银屑病有关;针对 IL-22 的治疗方法可能有望成为治疗银屑病的潜在治疗靶点。在本综述中,我们总结了 IL-22 在银屑病发病机制和治疗中的最新进展。

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