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1
Parallel expansion of human virus-specific FoxP3- effector memory and de novo-generated FoxP3+ regulatory CD8+ T cells upon antigen recognition in vitro.体外抗原识别后,人类病毒特异性FoxP3效应记忆细胞和新生FoxP3 +调节性CD8 + T细胞的平行扩增。
J Immunol. 2007 Jul 15;179(2):1039-48. doi: 10.4049/jimmunol.179.2.1039.
2
Human leukocyte antigen-associated sequence polymorphisms in hepatitis C virus reveal reproducible immune responses and constraints on viral evolution.丙型肝炎病毒中人类白细胞抗原相关序列多态性揭示了可重复的免疫反应及对病毒进化的限制。
Hepatology. 2007 Aug;46(2):339-49. doi: 10.1002/hep.21702.
3
Absence of viral escape within a frequently recognized HLA-A26-restricted CD8+ T-cell epitope targeting the functionally constrained hepatitis C virus NS5A/5B cleavage site.在一个常见的靶向功能受限的丙型肝炎病毒NS5A/5B切割位点的HLA - A26限制性CD8 + T细胞表位内未出现病毒逃逸。
J Gen Virol. 2007 Jul;88(Pt 7):1986-1991. doi: 10.1099/vir.0.82826-0.
4
Protective effect of HLA-B57 on HCV genotype 2 infection in a West African population.HLA - B57对西非人群丙型肝炎病毒2型感染的保护作用。
J Med Virol. 2007 Jun;79(6):724-33. doi: 10.1002/jmv.20848.
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Quantification and localisation of FOXP3+ T lymphocytes and relation to hepatic inflammation during chronic HCV infection.慢性丙型肝炎病毒感染期间FOXP3 + T淋巴细胞的定量、定位及其与肝脏炎症的关系。
J Hepatol. 2007 Sep;47(3):316-24. doi: 10.1016/j.jhep.2007.03.023. Epub 2007 Apr 12.
6
Decrease and dysfunction of dendritic cells correlate with impaired hepatitis C virus-specific CD4+ T-cell proliferation in patients with hepatitis C virus infection.在丙型肝炎病毒感染患者中,树突状细胞的减少和功能障碍与丙型肝炎病毒特异性CD4 + T细胞增殖受损相关。
Immunology. 2007 Jun;121(2):283-92. doi: 10.1111/j.1365-2567.2007.02577.x.
7
Founder effects in the assessment of HIV polymorphisms and HLA allele associations.HIV多态性评估及HLA等位基因关联中的奠基者效应
Science. 2007 Mar 16;315(5818):1583-6. doi: 10.1126/science.1131528.
8
IL-10, T cell exhaustion and viral persistence.白细胞介素-10、T细胞耗竭与病毒持续性
Trends Microbiol. 2007 Apr;15(4):143-6. doi: 10.1016/j.tim.2007.02.006. Epub 2007 Mar 1.
9
Impact of aboriginal ethnicity on HCV core-induced IL-10 synthesis: interaction with IL-10 gene polymorphisms.原住民种族对丙型肝炎病毒核心蛋白诱导的白细胞介素-10合成的影响:与白细胞介素-10基因多态性的相互作用
Hepatology. 2007 Mar;45(3):623-30. doi: 10.1002/hep.21511.
10
Dysfunction and functional restoration of HCV-specific CD8 responses in chronic hepatitis C virus infection.慢性丙型肝炎病毒感染中HCV特异性CD8反应的功能障碍与功能恢复
Hepatology. 2007 Mar;45(3):588-601. doi: 10.1002/hep.21541.

丙型肝炎病毒感染中导致CD8 + T细胞功能衰竭的宿主和病毒因素。

Host and viral factors contributing to CD8+ T cell failure in hepatitis C virus infection.

作者信息

Neumann-Haefelin Christoph, Spangenberg Hans-Christian, Blum Hubert-E, Thimme Robert

机构信息

Department of Medicine II, University Hospital Freiburg, Hugstetter Strasse 55, Freiburg D-79106, Germany.

出版信息

World J Gastroenterol. 2007 Sep 28;13(36):4839-47. doi: 10.3748/wjg.v13.i36.4839.

DOI:10.3748/wjg.v13.i36.4839
PMID:17828815
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4611762/
Abstract

Virus-specific CD8+ T cells are thought to be the major anti-viral effector cells in hepatitis C virus (HCV) infection. Indeed, viral clearance is associated with vigorous CD8+ T cell responses targeting multiple epitopes. In the chronic phase of infection, HCV-specific CD8+ T cell responses are usually weak, narrowly focused and display often functional defects regarding cytotoxicity, cytokine production, and proliferative capacity. In the last few years, different mechanisms which might contribute to the failure of HCV-specific CD8+ T cells in chronic infection have been identified, including insufficient CD4+ help, deficient CD8+ T cell differentiation, viral escape mutations, suppression by viral factors, inhibitory cytokines, inhibitory ligands, and regulatory T cells. In addition, host genetic factors such as the host's human leukocyte antigen (HLA) background may play an important role in the efficiency of the HCV-specific CD8+ T cell response and thus outcome of infection. The growing understanding of the mechanisms contributing to T cell failure and persistence of HCV infection will contribute to the development of successful immunotherapeutical and -prophylactical strategies.

摘要

病毒特异性CD8 + T细胞被认为是丙型肝炎病毒(HCV)感染中的主要抗病毒效应细胞。事实上,病毒清除与针对多个表位的强烈CD8 + T细胞反应相关。在感染的慢性期,HCV特异性CD8 + T细胞反应通常较弱,范围狭窄,并且在细胞毒性、细胞因子产生和增殖能力方面常常表现出功能缺陷。在过去几年中,已经确定了可能导致HCV特异性CD8 + T细胞在慢性感染中功能衰竭的不同机制,包括CD4 +辅助不足、CD8 + T细胞分化缺陷、病毒逃逸突变、病毒因子抑制、抑制性细胞因子、抑制性配体和调节性T细胞。此外,宿主遗传因素,如宿主的人类白细胞抗原(HLA)背景,可能在HCV特异性CD8 + T细胞反应的效率以及感染结果中发挥重要作用。对导致T细胞功能衰竭和HCV感染持续存在的机制的日益了解将有助于成功开发免疫治疗和预防策略。