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由于CD8 + T细胞成熟受损导致免疫控制失败:CD27可能提供一条线索。

Failing immune control as a result of impaired CD8+ T-cell maturation: CD27 might provide a clue.

作者信息

van Baarle Debbie, Kostense Stefan, van Oers Marinus H J, Hamann Dorte, Miedema Frank

机构信息

Dept of Clinical Viro-Immunology, Sanquin Research at CLB & Landsteiner Laboratory of the Academic Medical Center, University of Amsterdam, The Netherlands.

出版信息

Trends Immunol. 2002 Dec;23(12):586-91. doi: 10.1016/s1471-4906(02)02326-8.

Abstract

Despite readily detectable virus-specific CD8(+) T cells in most HIV-infected patients, immune surveillance is eventually lost, leading to progression to AIDS. Recently developed insights into human T-cell differentiation have been used to study the phenotype of virus-specific T cells in HIV-infected individuals. Based on these results, we propose that failing immune control in human viral infection could be a result of impaired cytotoxic T-lymphocyte (CTL) maturation into fully differentiated effector T cells. Impaired maturation is not confined to HIV-specific CD8(+) T cells but could also be involved in failing immunity to Epstein-Barr virus and other viral infections. We postulate that CD27(-) effector CD8(+) T cells might be required for adequate control of chronic viral infection and prevention of disease development.

摘要

尽管在大多数HIV感染患者中可轻易检测到病毒特异性CD8(+) T细胞,但免疫监视最终仍会丧失,导致病情发展为艾滋病。最近对人类T细胞分化的深入了解已被用于研究HIV感染个体中病毒特异性T细胞的表型。基于这些结果,我们提出人类病毒感染中免疫控制失败可能是由于细胞毒性T淋巴细胞(CTL)成熟为完全分化的效应T细胞受损所致。成熟受损不仅限于HIV特异性CD8(+) T细胞,也可能与对EB病毒和其他病毒感染的免疫失败有关。我们推测,CD27(-)效应性CD8(+) T细胞可能是充分控制慢性病毒感染和预防疾病发展所必需的。

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