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IL-33/ST2 信号通路在系统性硬化症及其他纤维化疾病中的作用。

Role of IL-33/ST2 signaling pathway in systemic sclerosis and other fibrotic diseases.

机构信息

Department of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.

Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, UK.

出版信息

Clin Exp Rheumatol. 2019 Jul-Aug;37 Suppl 119(4):141-146. Epub 2019 Sep 3.

Abstract

Systemic sclerosis (SSc) is a complex autoimmune disease characterised by fibrosis of the skin and multiple internal organs. Interleukin 33 (IL-33) has recently been investigated as a potential key player in the pathogenesis of SSc and other fibrotic diseases, owing to its effects on tissue fibrosis. Understanding how IL-33 is regulated and how it contributes to the development of fibrosis will be important to elucidate disease pathogenesis and may shed light on new areas for therapeutic development for patients. Here we discuss the recent research progress in our understanding of the role and the underlying mechanisms of IL-33/ST2 signaling pathway in SSc and other fibrotic diseases.

摘要

系统性硬化症(SSc)是一种复杂的自身免疫性疾病,其特征是皮肤和多个内脏器官纤维化。白细胞介素 33(IL-33)最近因其对组织纤维化的影响而被研究为 SSc 和其他纤维化疾病发病机制中的一个潜在关键因素。了解 IL-33 的调节方式以及它如何促进纤维化的发展对于阐明疾病发病机制非常重要,并且可能为患者的治疗开发开辟新的领域。在这里,我们讨论了我们对 IL-33/ST2 信号通路在 SSc 和其他纤维化疾病中的作用及其潜在机制的最新研究进展。

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