Jo Norihide, Zhang Rui, Ueno Hideki, Yamamoto Takuya, Weiskopf Daniela, Nagao Miki, Yamanaka Shinya, Hamazaki Yoko
Department of Life Science Frontiers, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.
Alliance Laboratory for Advanced Medical Research, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Front Aging. 2021 Aug 10;2:719342. doi: 10.3389/fragi.2021.719342. eCollection 2021.
Age is a major risk factor for COVID-19 severity, and T cells play a central role in anti-SARS-CoV-2 immunity. Because SARS-CoV-2-cross-reactive T cells have been detected in unexposed individuals, we investigated the age-related differences in pre-existing SARS-CoV-2-reactive T cells. SARS-CoV-2-reactive CD4 T cells from young and elderly individuals were mainly detected in the central memory fraction and exhibited similar functionalities and numbers. Naïve-phenotype SARS-CoV-2-reactive CD8 T cell populations decreased markedly in the elderly, while those with terminally differentiated and senescent phenotypes increased. Furthermore, senescent SARS-CoV-2-reactive CD8 T cell populations were higher in cytomegalovirus seropositive young individuals compared to seronegative ones. Our findings suggest that age-related differences in pre-existing SARS-CoV-2-reactive CD8 T cells may explain the poor outcomes in elderly patients and that cytomegalovirus infection is a potential factor affecting CD8 T cell immunity against SARS-CoV-2. Thus, this study provides insights for developing effective therapeutic and vaccination strategies for the elderly.
年龄是新冠病毒疾病严重程度的主要风险因素,而T细胞在抗SARS-CoV-2免疫中发挥核心作用。由于在未接触过病毒的个体中已检测到SARS-CoV-2交叉反应性T细胞,我们研究了预先存在的SARS-CoV-2反应性T细胞的年龄相关差异。年轻和老年个体的SARS-CoV-2反应性CD4 T细胞主要在中央记忆亚群中被检测到,并且表现出相似的功能和数量。幼稚表型的SARS-CoV-2反应性CD8 T细胞群体在老年人中显著减少,而终末分化和衰老表型的细胞群体增加。此外,与血清阴性的年轻个体相比,巨细胞病毒血清阳性的年轻个体中衰老的SARS-CoV-2反应性CD8 T细胞群体更多。我们的研究结果表明,预先存在的SARS-CoV-2反应性CD8 T细胞的年龄相关差异可能解释老年患者预后较差的原因,并且巨细胞病毒感染是影响CD8 T细胞对SARS-CoV-2免疫的一个潜在因素。因此,本研究为为老年人制定有效的治疗和疫苗接种策略提供了思路。