Programme in Emerging Infectious Diseases, Duke-NUS Medical School, 8 College Road, Singapore 169857, Singapore; Singapore Immunology Network, A(∗)STAR, Singapore, Singapore.
Programme in Emerging Infectious Diseases, Duke-NUS Medical School, 8 College Road, Singapore 169857, Singapore.
Immunity. 2022 Oct 11;55(10):1764-1778. doi: 10.1016/j.immuni.2022.08.008. Epub 2022 Aug 18.
Since the onset of the coronavirus disease 2019 (COVID-19) pandemic, multiple severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants with increasing ability to evade neutralizing antibodies have emerged. Thus, earlier interest in defining the correlates of protection from infection, mainly mediated by humoral immunity, has shifted to correlates of protection from disease, which require a more comprehensive analysis of both humoral and cellular immunity. In this review, we summarized the evidence that supports the role of SARS-CoV-2-specific T cells induced by infection, by vaccination or by their combination (defined as hybrid immunity) in disease protection. We then analyzed the different epidemiological and virological variables that can modify the magnitude, function, and anatomical localization of SARS-CoV-2-specific T cells and their influence in the possible ability of T cells to protect the host from severe COVID-19 development.
自 2019 年冠状病毒病(COVID-19)大流行以来,具有越来越强逃避中和抗体能力的多种严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)变异株已经出现。因此,人们对感染主要由体液免疫介导的保护相关因素的早期关注已经转移到对疾病保护的相关因素,这需要对体液免疫和细胞免疫进行更全面的分析。在这篇综述中,我们总结了支持由感染、接种疫苗或两者结合(定义为混合免疫)诱导的 SARS-CoV-2 特异性 T 细胞在疾病保护中的作用的证据。然后,我们分析了不同的流行病学和病毒学变量,这些变量可以改变 SARS-CoV-2 特异性 T 细胞的数量、功能和解剖定位及其对 T 细胞可能保护宿主免受严重 COVID-19 发展的影响。