Verhoeven David, Teijaro John R, Farber Donna L
Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
Viral Immunol. 2008 Jun;21(2):99-113. doi: 10.1089/vim.2008.0002.
Memory T cells are generated following an initial viral infection, and have the potential for mediating robust protective immunity to viral re-challenge due to their rapid and enhanced functional responses. In recent years, it has become clear that the memory T cell response to most viruses is remarkably diverse in phenotype, function, and tissue distribution, and can undergo dynamic changes during its long-term maintenance in vivo. However, the role of this variegation and compartmentalizationof memory T cells in protective immunity to viruses remains unclear. In this review,we discuss the diverse features of memory T cells that can delineate different subsets, the characteristics of memory T cells thus far identified to promote protective immune responses, and how the heterogeneous nature of memory T cells may also promote immunopathology during antiviral responses. We propose that given the profound heterogeneity of memory T cells, regulation of memory T cells during secondary responses could focus the response to participation of specific subsets,and/or inhibit memory T-cell subsets and functions that can lead to immunopathology.
记忆T细胞在初次病毒感染后产生,由于其快速且增强的功能反应,具有介导对病毒再次攻击的强大保护性免疫的潜力。近年来,很明显记忆T细胞对大多数病毒的反应在表型、功能和组织分布上具有显著多样性,并且在其体内长期维持过程中会发生动态变化。然而,记忆T细胞的这种多样化和区室化在病毒保护性免疫中的作用仍不清楚。在这篇综述中,我们讨论了可区分不同亚群的记忆T细胞的多样特征、迄今已确定的促进保护性免疫反应的记忆T细胞的特征,以及记忆T细胞的异质性如何在抗病毒反应过程中也促进免疫病理学。我们提出,鉴于记忆T细胞的深刻异质性,二次反应期间对记忆T细胞的调节可以将反应集中于特定亚群的参与,和/或抑制可导致免疫病理学的记忆T细胞亚群和功能。