Division of Rheumatology, Department of Medicine, Perelman School of Medicine, Institute for Immunology, University of Pennsylvania, Philadelphia, PA.
Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA.
Immunohorizons. 2023 Jul 1;7(7):543-553. doi: 10.4049/immunohorizons.2200003.
Immunological experiences lead to the development of specific T and B cell memory, which readies the host for a later pathogen rechallenge. Currently, immunological memory is best understood as a linear process whereby memory responses are generated by and directed against the same pathogen. However, numerous studies have identified memory cells that target pathogens in unexposed individuals. How "pre-existing memory" forms and impacts the outcome of infection remains unclear. In this review, we discuss differences in the composition of baseline T cell repertoire in mice and humans, factors that influence pre-existing immune states, and recent literature on their functional significance. We summarize current knowledge on the roles of pre-existing T cells in homeostasis and perturbation and their impacts on health and disease.
免疫经历导致特定的 T 细胞和 B 细胞记忆的形成,使宿主对随后的病原体再感染做好准备。目前,免疫记忆被很好地理解为一个线性过程,其中记忆反应由相同的病原体产生并针对该病原体。然而,许多研究已经鉴定出针对未暴露个体中的病原体的记忆细胞。“预先存在的记忆”如何形成以及如何影响感染的结果尚不清楚。在这篇综述中,我们讨论了小鼠和人类中基础 T 细胞库组成的差异、影响预先存在的免疫状态的因素,以及最近关于其功能意义的文献。我们总结了预先存在的 T 细胞在稳态和干扰中的作用及其对健康和疾病的影响的现有知识。