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宿主-微生物相互作用中由腺苷介导的免疫改变。

Immunological alterations mediated by adenosine during host-microbial interactions.

机构信息

Division of Gastroenterology and Hepatology, Department of Medicine, University of Virginia, Charlottesville, 22908-0708, USA.

出版信息

Immunol Res. 2011 May;50(1):69-77. doi: 10.1007/s12026-011-8207-0.

Abstract

Adenosine accumulates in inflammation and ischemia but it is more than an end-product of ATP catabolism. Signaling through different receptors with distinct, cell-specific cytoplasmic pathways, adenosine is now recognized as an inducible switch that regulates the immune system. By acting through the A(2A)AR, adenosine shapes T cell function, largely by conferring an anti-inflammatory tone on effector Th cells (Teff) and natural killer (NK)T cells. In contrast, both the A(2A)AR and A(2B)AR are expressed by antigen-presenting cells (APC) which have been shown to regulate innate responses and the transition to adaptive immunity. There is also emerging evidence that adenosine production is one mechanism that allows some pathogens as well as neoplasms to evade host defenses. This review discusses the immunoregulatory functions of adenosine and some of the interactions it may have in regulating host-microbial interactions.

摘要

腺苷在炎症和缺血中积累,但它不仅仅是 ATP 分解代谢的终产物。通过不同的受体传递信号,这些受体具有不同的、细胞特异性的细胞质途径,腺苷现在被认为是一种诱导开关,调节免疫系统。通过与 A(2A)AR 结合,腺苷调节 T 细胞的功能,主要是通过赋予效应 Th 细胞 (Teff) 和自然杀伤 (NK)T 细胞抗炎表型。相比之下,A(2A)AR 和 A(2B)AR 都由抗原呈递细胞 (APC) 表达,已证明 APC 可以调节固有免疫反应和向适应性免疫的转变。越来越多的证据表明,腺苷的产生是某些病原体以及肿瘤逃避宿主防御的一种机制。本文讨论了腺苷的免疫调节功能及其在调节宿主-微生物相互作用中的一些相互作用。

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