Psoriatic arthritis under the influence of IFNγ.

Psoriatic arthritis under the influence of IFNγ.
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DOI:
10.1016/j.clim.2020.108513
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发表时间:
2020-09
期刊:
Clinical immunology (Orlando, Fla.)
影响因子:
--
通讯作者:
Adamopoulos IE
Adamopoulos IE
中科院分区:
其他
文献类型:
--
作者:
Dai H;Adamopoulos IE

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银屑病是一种常见的多因素自身免疫性皮肤病,在很大比例的患者中,免疫反应涉及指甲和关节病理,其发展为银屑病关节炎(PsA)。历史上,T辅助细胞1(Th 1)-衍生的IFN-γ在银屑病皮肤中大量检测到,并且其与PsO的发展和严重程度相关,导致银屑病早期分类为Th 1介导的疾病。近年来对PsO发病机制的细胞和分子机制的研究,以及针对白细胞介素17 A(IL-17)的生物制剂的令人印象深刻的结果,已经将焦点转移到IL-17 A上。然而,IFN-γ在IL-17诱导的病理学中的贡献及其在PsA发展中的参与在很大程度上被掩盖了。本文综述了IFN-γ的研究进展,并就IFN-γ在PsO和PsA疾病发病机制中的作用提供了新的见解。
Psoriasis is a common multifactorial autoimmune disease of the skin, and in a large percentage of patients, immune responses involve nail and joint pathology, which develop psoriatic arthritis (PsA). Historically, T helper 1 (Th1)-derived-IFN-γ was abundantly detected in psoriatic skin and its correlation with development and severity of PsO, led to an early classification of psoriasis as a Th1-mediated disease. Investigations of the cellular and molecular mechanisms of PsO pathogenesis in recent years, together with impressive results of biologics against interleukin 17 A (IL-17) have shifted focus on IL-17A. However, the contributions of IFN-γ in IL-17 induced pathology and its involvement in the development of PsA have been largely overshadowed. This review summarizes the current knowledge on IFN-γ and provides new insights on the contribution of IFN-γ to PsO and PsA disease pathogenesis and development.
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发表时间: 1995-06-15
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