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特发性肺纤维化急性加重的免疫机制

The immune mechanisms of acute exacerbations of idiopathic pulmonary fibrosis.

作者信息

Chen Tao, Sun Wei, Xu Zuo-Jun

机构信息

Department of Respiratory and Critical Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Department of Respiratory and Critical Medicine, The second hospital of Tianjin Medical University, Tianjin, China.

出版信息

Front Immunol. 2024 Dec 16;15:1450688. doi: 10.3389/fimmu.2024.1450688. eCollection 2024.

Abstract

Acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF) are the leading cause of mortality among patients with IPF. There is still a lack of effective treatments for AE-IPF, resulting in a hospitalization mortality rate as high as 70%-80%. To reveal the complicated mechanism of AE-IPF, more attention has been paid to its disturbed immune environment, as patients with IPF exhibit deficiencies in pathogen defense due to local immune dysregulation. During the development of AE-IPF, the classical stimulatory signals in adaptive immunity are inhibited, while the nonclassical immune reactions (Th17) are activated, attracting numerous neutrophils and monocytes to lung tissues. However, there is limited information about the specific changes in the immune response of AE-IPF. We summarized the immune mechanisms of AE-IPF in this review.

摘要

特发性肺纤维化急性加重(AE-IPF)是IPF患者死亡的主要原因。目前仍缺乏针对AE-IPF的有效治疗方法,导致住院死亡率高达70%-80%。为揭示AE-IPF的复杂机制,人们越来越关注其紊乱的免疫环境,因为IPF患者由于局部免疫失调而在病原体防御方面存在缺陷。在AE-IPF的发展过程中,适应性免疫中的经典刺激信号受到抑制,而非经典免疫反应(Th17)被激活,吸引大量中性粒细胞和单核细胞进入肺组织。然而,关于AE-IPF免疫反应的具体变化的信息有限。我们在本综述中总结了AE-IPF的免疫机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3147/11682984/00df12f30bd3/fimmu-15-1450688-g001.jpg

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