体内由IFNγ介导的TCR非依赖性抑制CD8(+) T细胞细胞因子产生

TCR independent suppression of CD8(+) T cell cytokine production mediated by IFNγ in vivo.

作者信息

Hosking Martin P, Flynn Claudia T, Whitton J Lindsay

机构信息

Dept. of Immunology and Microbial Science, SP30-2110, The Scripps Research Institute, 10550 N. Torrey Pines Rd., La Jolla, CA 92037, USA.

Dept. of Immunology and Microbial Science, SP30-2110, The Scripps Research Institute, 10550 N. Torrey Pines Rd., La Jolla, CA 92037, USA.

出版信息

Virology. 2016 Nov;498:69-81. doi: 10.1016/j.virol.2016.08.003. Epub 2016 Aug 24.

Abstract

CD8(+) memory T cells produce IFNγ within hours of secondary infection, but this is quickly terminated in vivo despite the presence of stimulatory viral antigen, suggesting that active suppression occurs. Herein, we investigated the in vivo effector function of CD8(+) memory T cells during successive encounters with viral antigen. CD8(+) T cells in immune mice receiving prior viral or peptide challenge failed to reproduce IFNγ during LCMV rechallenge. Surprisingly, this refractory state was induced even in memory cells that had not encountered their cognate antigen, indicating that the silencing of CD8(+) T cell responses is TCR-independent. Direct injection of IFNγ also suppressed the ability of virus-specific memory cells to respond to subsequent viral challenge. We propose the existence of a negative feedback loop whereby IFNγ, produced by memory CD8(+) T cells to combat viral challenge, acts - directly or indirectly - to limit its further production.

摘要

CD8(+)记忆T细胞在再次感染数小时内即可产生γ干扰素,但尽管存在刺激性病毒抗原,其在体内的产生会迅速终止,提示存在主动抑制作用。在此,我们研究了CD8(+)记忆T细胞在连续接触病毒抗原过程中的体内效应功能。接受过病毒或肽类攻击的免疫小鼠中的CD8(+) T细胞在淋巴细胞脉络丛脑膜炎病毒再次攻击期间无法再次产生γ干扰素。令人惊讶的是,即使在尚未遇到其同源抗原的记忆细胞中也会诱导出这种不应答状态,这表明CD8(+) T细胞应答的沉默与TCR无关。直接注射γ干扰素也会抑制病毒特异性记忆细胞对后续病毒攻击作出反应的能力。我们提出存在一种负反馈回路,即记忆性CD8(+) T细胞产生的γ干扰素在对抗病毒攻击时,直接或间接地作用于限制其进一步产生。

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