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本文引用的文献

1
Role of interferon regulatory factor 7 in T cell responses during acute lymphocytic choriomeningitis virus infection.干扰素调节因子 7 在急性淋巴细胞性脉络丛脑膜炎病毒感染期间 T 细胞反应中的作用。
J Virol. 2012 Oct;86(20):11254-65. doi: 10.1128/JVI.00576-12. Epub 2012 Aug 8.
2
Signal 3 cytokines as modulators of primary immune responses during infections: the interplay of type I IFN and IL-12 in CD8 T cell responses.信号 3 细胞因子作为感染期间初级免疫应答的调节剂:I 型 IFN 和 IL-12 在 CD8 T 细胞应答中的相互作用。
PLoS One. 2012;7(7):e40865. doi: 10.1371/journal.pone.0040865. Epub 2012 Jul 17.
3
Timing and magnitude of type I interferon responses by distinct sensors impact CD8 T cell exhaustion and chronic viral infection.不同传感器的 I 型干扰素反应的时间和幅度影响 CD8 T 细胞耗竭和慢性病毒感染。
Cell Host Microbe. 2012 Jun 14;11(6):631-42. doi: 10.1016/j.chom.2012.05.003.
4
Presensitizing with a Toll-like receptor 3 ligand impairs CD8 T-cell effector differentiation and IL-33 responsiveness.预先致敏 Toll 样受体 3 配体可损害 CD8 T 细胞效应分化和 IL-33 反应性。
Proc Natl Acad Sci U S A. 2012 Jun 26;109(26):10486-91. doi: 10.1073/pnas.1202607109. Epub 2012 Jun 11.
5
Interleukin-1R signaling is essential for induction of proapoptotic CD8 T cells, viral clearance, and pathology during lymphocytic choriomeningitis virus infection in mice.白细胞介素-1R 信号对于诱导细胞凋亡的 CD8 T 细胞、病毒清除以及小鼠淋巴细胞性脉络丛脑膜炎病毒感染期间的病理学至关重要。
J Virol. 2012 Aug;86(16):8713-9. doi: 10.1128/JVI.00682-12. Epub 2012 Jun 6.
6
Regulation of innate CD8+ T-cell activation mediated by cytokines.细胞因子调节固有 CD8+T 细胞的激活。
Proc Natl Acad Sci U S A. 2012 Jun 19;109(25):9971-6. doi: 10.1073/pnas.1203543109. Epub 2012 Jun 4.
7
Antigen amount dictates CD8+ T-cell exhaustion during chronic viral infection irrespective of the type of antigen presenting cell.抗原数量决定了慢性病毒感染期间 CD8+ T 细胞的耗竭,而与抗原提呈细胞的类型无关。
Eur J Immunol. 2012 Sep;42(9):2290-304. doi: 10.1002/eji.201142275. Epub 2012 Aug 6.
8
Therapeutic blockade of transforming growth factor beta fails to promote clearance of a persistent viral infection.治疗性阻断转化生长因子-β未能促进持续性病毒感染的清除。
J Virol. 2012 Jul;86(13):7060-71. doi: 10.1128/JVI.00164-12. Epub 2012 May 2.
9
Treatment with IL-7 prevents the decline of circulating CD4+ T cells during the acute phase of SIV infection in rhesus macaques.白细胞介素-7(IL-7)治疗可防止恒河猴感染 SIV 急性期中循环 CD4+ T 细胞的下降。
PLoS Pathog. 2012;8(4):e1002636. doi: 10.1371/journal.ppat.1002636. Epub 2012 Apr 12.
10
Long-lived epithelial immunity by tissue-resident memory T (TRM) cells in the absence of persisting local antigen presentation.组织驻留记忆 T(TRM)细胞在不存在持续局部抗原呈递的情况下实现长寿命上皮免疫。
Proc Natl Acad Sci U S A. 2012 May 1;109(18):7037-42. doi: 10.1073/pnas.1202288109. Epub 2012 Apr 16.

抗病毒 CD8 T 细胞和它们所爱的细胞因子。

Anti-viral CD8 T cells and the cytokines that they love.

机构信息

Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

出版信息

Virology. 2013 Jan 5;435(1):157-69. doi: 10.1016/j.virol.2012.09.012.

DOI:10.1016/j.virol.2012.09.012
PMID:23217625
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3580945/
Abstract

Viral infections cause an immunological disequilibrium that provokes CD8 T cell responses. These cells play critical roles in purging acute infections, limiting persistent infections, and conferring life-long protective immunity. At every stage of the response anti-viral CD8 T cells are sensitive to signals from cytokines. Initially cytokines operate as immunological warning signs that inform of the presence of an infection, and also influence the developmental choices of the responding cells. Later during the course of the response other sets of cytokines support the survival and maintenance of the differentiated anti-viral CD8 T cells. Although many cytokines promote virus-specific CD8 T cells, other cytokines can suppress their activities and thus favor viral persistence. In this review we discuss how select cytokines act to regulate anti-viral CD8 T cells throughout the response and influence the outcome of viral infections.

摘要

病毒感染会导致免疫失衡,从而引发 CD8 T 细胞应答。这些细胞在清除急性感染、限制持续性感染和提供终身保护免疫方面发挥着关键作用。在抗病毒 CD8 T 细胞反应的每个阶段,细胞因子信号都很敏感。最初,细胞因子作为免疫警示信号,提示感染的存在,并影响反应细胞的发育选择。在反应过程的后期,其他细胞因子集支持分化的抗病毒 CD8 T 细胞的存活和维持。虽然许多细胞因子促进病毒特异性 CD8 T 细胞,但其他细胞因子可以抑制它们的活性,从而有利于病毒的持续存在。在这篇综述中,我们讨论了选择细胞因子如何在整个反应过程中调节抗病毒 CD8 T 细胞,并影响病毒感染的结果。