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T细胞辅助增强CD8(+)树突状细胞中的固有信号,以实现最佳的CD8(+) T细胞启动。

T Cell Help Amplifies Innate Signals in CD8(+) DCs for Optimal CD8(+) T Cell Priming.

作者信息

Greyer Marie, Whitney Paul G, Stock Angus T, Davey Gayle M, Tebartz Christina, Bachem Annabell, Mintern Justine D, Strugnell Richard A, Turner Stephen J, Gebhardt Thomas, O'Keeffe Meredith, Heath William R, Bedoui Sammy

机构信息

Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, VIC 3010, Australia.

Department of Biochemistry and Molecular Biology, University of Melbourne, Parkville, VIC 3010, Australia.

出版信息

Cell Rep. 2016 Jan 26;14(3):586-597. doi: 10.1016/j.celrep.2015.12.058. Epub 2016 Jan 7.

Abstract

DCs often require stimulation from CD4(+) T cells to propagate CD8(+) T cell responses, but precisely how T cell help optimizes the priming capacity of DCs and why this appears to differ between varying types of CD8(+) T cell immunity remains unclear. We show that CD8(+) T cell priming upon HSV-1 skin infection depended on DCs receiving stimulation from both IFN-α/β and CD4(+) T cells to provide IL-15. This was not an additive effect but resulted from CD4(+) T cells amplifying DC production of IL-15 in response to IFN-α/β. We also observed that increased innate stimulation reversed the helper dependence of CD8(+) T cell priming and that the innate stimulus, rather than the CD4(+) T cells themselves, determined how "help'" was integrated into the priming response by DCs. These findings identify T cell help as a flexible means to amplify varying suboptimal innate signals in DCs.

摘要

树突状细胞(DCs)通常需要CD4(+) T细胞的刺激来促进CD8(+) T细胞反应,但T细胞辅助究竟如何优化DCs的启动能力,以及为何在不同类型的CD8(+) T细胞免疫中似乎存在差异,目前尚不清楚。我们发现,单纯疱疹病毒1型(HSV-1)皮肤感染后的CD8(+) T细胞启动依赖于DCs同时接受IFN-α/β和CD4(+) T细胞的刺激以提供白细胞介素-15(IL-15)。这并非是一种累加效应,而是CD4(+) T细胞响应IFN-α/β放大了DCs产生IL-15的能力。我们还观察到,增强的固有刺激逆转了CD8(+) T细胞启动对辅助的依赖性,并且固有刺激而非CD4(+) T细胞本身决定了“辅助”是如何被DCs整合到启动反应中的。这些发现表明,T细胞辅助是一种灵活的方式,可放大DCs中不同的次优固有信号。

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