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Selection of high-avidity CD8 T cells correlates with control of hepatitis C virus infection.高亲和力CD8 T细胞的选择与丙型肝炎病毒感染的控制相关。
Hepatology. 2008 Sep;48(3):713-22. doi: 10.1002/hep.22379.
2
Detection of low avidity CD8(+) T cell populations with coreceptor-enhanced peptide-major histocompatibility complex class I tetramers.使用共受体增强的肽-主要组织相容性复合体I类四聚体检测低亲和力CD8(+) T细胞群体。
J Immunol Methods. 2008 Sep 30;338(1-2):31-9. doi: 10.1016/j.jim.2008.07.008. Epub 2008 Jul 31.
3
Impact of MHC class I diversity on immune control of immunodeficiency virus replication.MHC I类多样性对免疫缺陷病毒复制免疫控制的影响。
Nat Rev Immunol. 2008 Aug;8(8):619-30. doi: 10.1038/nri2357.
4
Defining the directionality and quality of influenza virus-specific CD8+ T cell cross-reactivity in individuals infected with hepatitis C virus.确定丙型肝炎病毒感染个体中流感病毒特异性CD8 + T细胞交叉反应的方向性和质量。
J Clin Invest. 2008 Mar;118(3):1143-53. doi: 10.1172/JCI33082.
5
Increased cytotoxic T-lymphocyte epitope variant cross-recognition and functional avidity are associated with hepatitis C virus clearance.细胞毒性T淋巴细胞表位变体交叉识别增加及功能亲和力与丙型肝炎病毒清除相关。
J Virol. 2008 Mar;82(6):3147-53. doi: 10.1128/JVI.02252-07. Epub 2008 Jan 9.
6
Single-molecule level analysis of the subunit composition of the T cell receptor on live T cells.活T细胞上T细胞受体亚基组成的单分子水平分析。
Proc Natl Acad Sci U S A. 2007 Nov 6;104(45):17662-7. doi: 10.1073/pnas.0700411104. Epub 2007 Oct 30.
7
Molecular signature of CD8+ T cell exhaustion during chronic viral infection.慢性病毒感染期间CD8 + T细胞耗竭的分子特征。
Immunity. 2007 Oct;27(4):670-84. doi: 10.1016/j.immuni.2007.09.006. Epub 2007 Oct 18.
8
Superior control of HIV-1 replication by CD8+ T cells is reflected by their avidity, polyfunctionality, and clonal turnover.CD8 + T细胞对HIV-1复制的卓越控制体现在它们的亲和力、多功能性和克隆更新上。
J Exp Med. 2007 Oct 1;204(10):2473-85. doi: 10.1084/jem.20070784. Epub 2007 Sep 24.
9
Cutting edge: CD8+ T cell clones possess the potential to differentiate into both high- and low-avidity effector cells.前沿:CD8 + T细胞克隆具有分化为高亲和力和低亲和力效应细胞的潜力。
J Immunol. 2007 Jul 15;179(2):748-51. doi: 10.4049/jimmunol.179.2.748.
10
Upregulation of PD-1 expression on circulating and intrahepatic hepatitis C virus-specific CD8+ T cells associated with reversible immune dysfunction.循环及肝内丙型肝炎病毒特异性CD8⁺ T细胞上PD-1表达上调与可逆性免疫功能障碍相关。
J Virol. 2007 Sep;81(17):9249-58. doi: 10.1128/JVI.00409-07. Epub 2007 Jun 13.

T 细胞敏感性与病毒感染的结果。

T cell sensitivity and the outcome of viral infection.

机构信息

Nuffield Department of Medicine and NIHR Biomedical Research Centre Programme, Peter Medawar Building for Pathogen Research, University of Oxford, Oxford, UK.

出版信息

Clin Exp Immunol. 2010 Mar;159(3):245-55. doi: 10.1111/j.1365-2249.2009.04047.x. Epub 2009 Dec 1.

DOI:10.1111/j.1365-2249.2009.04047.x
PMID:19968665
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2819491/
Abstract

The importance of CD8(+) T cells in the control of viral infections is well established. However, what differentiates CD8(+) T cell responses in individuals who control infection and those who do not is not well understood. 'Functional sensitivity' describes an important quality of the T cell response and is determined in part by the affinity of the T cell receptor for antigen. A more sensitive T cell response is generally believed to be more efficient and associated with better control of viral infection, yet may also drive viral mutation and immune escape. Various in vitro techniques have been used to measure T cell sensitivity; however, rapid ex vivo analysis of this has been made possible by the application of the 'magic' tetramer technology. Such tools have potentially important applications in the design and evaluation of vaccines.

摘要

CD8(+) T 细胞在控制病毒感染中的重要性已得到充分证实。然而,控制感染和不控制感染的个体之间的 CD8(+) T 细胞反应的区别尚不清楚。“功能敏感性”描述了 T 细胞反应的一个重要质量,部分取决于 T 细胞受体对抗原的亲和力。通常认为,更敏感的 T 细胞反应更有效,与更好地控制病毒感染相关,但也可能导致病毒突变和免疫逃逸。已经使用了各种体外技术来测量 T 细胞敏感性;然而,通过应用“神奇”四聚体技术,已经可以快速在体外进行这种分析。这些工具在疫苗的设计和评估中具有潜在的重要应用。