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非肽类异戊烯焦磷酸抗原直接呈递给人γδ T细胞。

Direct presentation of nonpeptide prenyl pyrophosphate antigens to human gamma delta T cells.

作者信息

Morita C T, Beckman E M, Bukowski J F, Tanaka Y, Band H, Bloom B R, Golan D E, Brenner M B

机构信息

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.

出版信息

Immunity. 1995 Oct;3(4):495-507. doi: 10.1016/1074-7613(95)90178-7.

Abstract

Human V gamma 2V delta 2+ T cells recognize mycobacterial nonpeptide antigens, such as isopentenyl pyrophosphate, and their synthetic analogs, such as monoethyl phosphate, through a TCR-dependent process. Here, we examine the presentation of these antigens. V gamma 2V delta 2+ T cells recognized secreted prenyl pyrophosphate antigens in the absence of other accessory cells but, under such conditions, required T cell-T cell contact. Recognition required neither the expression of classical MHC class I, MHC class II, or CD1a, CD1b, and CD1c molecules, nor MHC class I or class II peptide loading pathways. Fixed accessory cells also presented the prenyl pyrophosphate antigens to gamma delta T cells. Thus, in contrast with the presentation of conventional peptide antigens, protein antigens, and superantigens to alpha beta T cells, prenyl pyrophosphate antigens are presented to gamma delta T cells through a novel extracellular pathway that does not require antigen uptake, antigen processing, or MHC class I or class II expression. This pathway allows for the rapid recognition of bacteria by gamma delta T cells and suggests that gamma delta T cells play a role in the early response to bacterial infection.

摘要

人类Vγ2Vδ2 + T细胞通过TCR依赖性过程识别分枝杆菌非肽抗原,如异戊烯基焦磷酸及其合成类似物,如磷酸单乙酯。在此,我们研究这些抗原的呈递。Vγ2Vδ2 + T细胞在没有其他辅助细胞的情况下识别分泌的异戊烯基焦磷酸抗原,但在这种条件下,需要T细胞与T细胞接触。识别既不需要经典的MHC I类、MHC II类或CD1a、CD1b和CD1c分子的表达,也不需要MHC I类或II类肽负载途径。固定的辅助细胞也将异戊烯基焦磷酸抗原呈递给γδT细胞。因此,与向αβT细胞呈递传统肽抗原、蛋白质抗原和超抗原不同,异戊烯基焦磷酸抗原通过一种不需要抗原摄取、抗原加工或MHC I类或II类表达的新型细胞外途径呈递给γδT细胞。该途径允许γδT细胞快速识别细菌,并表明γδT细胞在对细菌感染的早期反应中起作用。

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