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血管炎中T细胞与巨噬细胞的相互作用及肉芽肿形成

T cell-macrophage interactions and granuloma formation in vasculitis.

作者信息

Hilhorst Marc, Shirai Tsuyoshi, Berry Gerald, Goronzy Jörg J, Weyand Cornelia M

机构信息

Division of Immunology and Rheumatology, Department of Medicine, Stanford University , Stanford, CA , USA.

Department of Pathology, Stanford University , Stanford, CA , USA.

出版信息

Front Immunol. 2014 Sep 12;5:432. doi: 10.3389/fimmu.2014.00432. eCollection 2014.

Abstract

Granuloma formation, bringing into close proximity highly activated macrophages and T cells, is a typical event in inflammatory blood vessel diseases, and is noted in the name of several of the vasculitides. It is not known whether specific properties of the microenvironment in the blood vessel wall or the immediate surroundings of blood vessels contribute to granuloma formation and, in some cases, generation of multinucleated giant cells. Granulomas provide a specialized niche to optimize macrophage-T cell interactions, strongly activating both cell types. This is mirrored by the intensity of the systemic inflammation encountered in patients with vasculitis, often presenting with malaise, weight loss, fever, and strongly upregulated acute phase responses. As a sophisticated and highly organized structure, granulomas can serve as an ideal site to induce differentiation and maturation of T cells. The granulomas possibly seed aberrant Th1 and Th17 cells into the circulation, which are known to be the main pathogenic cells in vasculitis. Through the induction of memory T cells, aberrant innate immune responses can imprint the host immune system for decades to come and promote chronicity of the disease process. Improved understanding of T cell-macrophage interactions will redefine pathogenic models in the vasculitides and provide new avenues for immunomodulatory therapy.

摘要

肉芽肿形成会使高度活化的巨噬细胞和T细胞紧密靠近,这是炎症性血管疾病中的典型事件,并且在几种血管炎的名称中有所体现。目前尚不清楚血管壁或血管紧邻区域的微环境的特定属性是否有助于肉芽肿形成,以及在某些情况下是否有助于多核巨细胞的产生。肉芽肿提供了一个特殊的微环境来优化巨噬细胞与T细胞的相互作用,从而强烈激活这两种细胞类型。这反映在血管炎患者所经历的全身炎症强度上,这些患者常表现出不适、体重减轻、发热以及急性期反应强烈上调。作为一种复杂且高度有组织的结构,肉芽肿可以作为诱导T细胞分化和成熟的理想场所。肉芽肿可能会将异常的Th1和Th17细胞播散到循环中,已知这些细胞是血管炎的主要致病细胞。通过诱导记忆T细胞,异常的先天免疫反应可能会在未来几十年影响宿主免疫系统,并促进疾病进程的慢性化。对T细胞与巨噬细胞相互作用的深入理解将重新定义血管炎的致病模型,并为免疫调节治疗提供新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/660d/4162471/b24b2ef1183b/fimmu-05-00432-g001.jpg

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