Laidlaw Brian J, Craft Joseph E, Kaech Susan M
Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, California 94143, USA.
Nat Rev Immunol. 2016 Feb;16(2):102-11. doi: 10.1038/nri.2015.10. Epub 2016 Jan 19.
Following infection, T cells differentiate into a heterogeneous population of effector T cells that can mediate pathogen clearance. A subset of these effector T cells possesses the ability to survive long term and mature into memory T cells that can provide long-term immunity. Understanding the signals that regulate the development of memory T cells is crucial to efforts to design vaccines capable of eliciting T cell-based immunity. CD4(+) T cells are essential in the formation of protective memory CD8(+) T cells following infection or immunization. However, until recently, the mechanisms by which CD4(+) T cells act to support memory CD8(+) T cell development following infection were unclear. Here, we discuss recent studies that provide insight into the multifaceted role of CD4(+) T cells in the regulation of memory CD8(+) T cell differentiation.
感染后,T细胞分化为一群异质性的效应T细胞,它们能够介导病原体清除。这些效应T细胞的一个亚群具有长期存活并成熟为记忆T细胞的能力,记忆T细胞可提供长期免疫。了解调节记忆T细胞发育的信号对于设计能够引发基于T细胞免疫的疫苗至关重要。CD4(+) T细胞在感染或免疫后保护性记忆CD8(+) T细胞的形成中至关重要。然而,直到最近,感染后CD4(+) T细胞支持记忆CD8(+) T细胞发育的机制仍不清楚。在这里,我们讨论了最近的研究,这些研究深入了解了CD4(+) T细胞在调节记忆CD8(+) T细胞分化中的多方面作用。