Kennedy Institute of Rheumatology, University of Oxford, OX3 7FY Oxford, United Kingdom.
Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016.
J Immunol. 2019 Aug 1;203(3):601-606. doi: 10.4049/jimmunol.1801687. Epub 2019 Jun 14.
Memory T cells are endowed with multiple functional features that enable them to be more protective than naive T cells against infectious threats. It is not known if memory cells have a higher synapse propensity (SP; i.e., increased probability to form immature immunological synapses that then provide an entry into different modes of durable interaction with APCs). In this study, we show that only human memory CD8 T cells have remarkably high SP compared with naive counterparts. Such a dichotomy between naive and memory cells is not observed within the human CD4 or murine CD8 T cell population. Higher SP in human memory CD8 T cells allows them to outcompete and prevent naive CD8 T cells from getting recruited to the response. This observation has implications for original antigenic sin and aging of the immune system in humans.
记忆 T 细胞具有多种功能特征,使它们比幼稚 T 细胞更能抵抗感染性威胁。目前尚不清楚记忆细胞是否具有更高的突触倾向(SP;即增加形成不成熟免疫突触的概率,然后为与 APC 进行不同模式的持久相互作用提供途径)。在这项研究中,我们表明,只有人类记忆 CD8 T 细胞具有明显高于幼稚细胞的 SP。在人类 CD4 或鼠 CD8 T 细胞群体中没有观察到这种幼稚细胞和记忆细胞之间的二分法。人类记忆 CD8 T 细胞中的高 SP 使其能够竞争并阻止幼稚 CD8 T 细胞被招募到反应中。这一观察结果对人类的原始抗原性和免疫系统衰老具有重要意义。