Center for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, the Netherlands.
Center for Translational Immunology, University Medical Center, Utrecht, the Netherlands.
Aging Cell. 2020 Nov;19(11):e13262. doi: 10.1111/acel.13262. Epub 2020 Oct 20.
Older adults often show signs of impaired CD8 T-cell immunity, reflected by weaker responses against new infections and vaccinations, and decreased protection against reinfection. This immune impairment is in part thought to be the consequence of a decrease in both T-cell numbers and repertoire diversity. If this is indeed the case, a strategy to prevent infectious diseases in older adults could be the induction of protective memory responses through vaccination at a younger age. However, this requires that the induced immune responses are maintained until old age. It is therefore important to obtain insights into the long-term maintenance of the antigen-specific T-cell repertoire. Here, we review the literature on the maintenance of antigen-experienced CD8 T-cell repertoires against acute and chronic infections. We describe the complex interactions that play a role in shaping the memory T-cell repertoire, and the effects of age, infection history, and T-cell avidity. We discuss the implications of these findings for the development of new vaccination strategies to protect older adults.
老年人通常表现出 CD8 T 细胞免疫受损的迹象,表现在对新感染和疫苗接种的反应较弱,以及对再感染的保护作用降低。这种免疫损伤部分被认为是 T 细胞数量和 repertoire 多样性减少的结果。如果情况确实如此,那么预防老年人传染病的策略可能是通过在年轻时接种疫苗来诱导保护性记忆反应。然而,这需要诱导的免疫反应能够维持到老年。因此,了解抗原特异性 T 细胞 repertoire 的长期维持非常重要。在这里,我们回顾了关于针对急性和慢性感染的抗原经验 CD8 T 细胞 repertoire 维持的文献。我们描述了在塑造记忆 T 细胞 repertoire 中起作用的复杂相互作用,以及年龄、感染史和 T 细胞亲和力的影响。我们讨论了这些发现对开发新的疫苗接种策略以保护老年人的影响。