Department of Immunology, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau (IIB Sant Pau), Universitat Autònoma de Barcelona, Barcelona, Spain.
Unidad de enfermedades infecciosas, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Front Immunol. 2022 Jun 27;13:904686. doi: 10.3389/fimmu.2022.904686. eCollection 2022.
Two years after the appearance of the SARS-CoV-2 virus, the causal agent of the current global pandemic, it is time to analyze the evolution of the immune protection that infection and vaccination provide. Cellular immunity plays an important role in limiting disease severity and the resolution of infection. The early appearance, breadth and magnitude of SARS-CoV-2 specific T cell response has been correlated with disease severity and it has been thought that T cell responses may be sufficient to clear infection with minimal disease in COVID-19 patients with X-linked or autosomal recessive agammaglobulinemia. However, our knowledge of the phenotypic and functional diversity of CD8+ cytotoxic lymphocytes, CD4+ T helper cells, mucosal-associated invariant T (MAIT) cells and CD4+ T follicular helper (Tfh), which play a critical role in infection control as well as long-term protection, is still evolving. It has been described how CD8+ cytotoxic lymphocytes interrupt viral replication by secreting antiviral cytokines (IFN-γ and TNF-α) and directly killing infected cells, negatively correlating with stages of disease progression. In addition, CD4+ T helper cells have been reported to be key pieces, leading, coordinating and ultimately regulating antiviral immunity. For instance, in some more severe COVID-19 cases a dysregulated CD4+ T cell signature may contribute to the greater production of pro-inflammatory cytokines responsible for pathogenic inflammation. Here we discuss how cellular immunity is the axis around which the rest of the immune system components revolve, since it orchestrates and leads antiviral response by regulating the inflammatory cascade and, as a consequence, the innate immune system, as well as promoting a correct humoral response through CD4+ Tfh cells. This review also analyses the critical role of cellular immunity in modulating the development of high-affinity neutralizing antibodies and germinal center B cell differentiation in memory and long-lived antibody secreting cells. Finally, since there is currently a high percentage of vaccinated population and, in some cases, vaccine booster doses are even being administered in certain countries, we have also summarized newer approaches to long-lasting protective immunity and the cross-protection of cellular immune response against SARS-CoV-2.
在出现 SARS-CoV-2 病毒(当前全球大流行的病原体)两年后,是时候分析感染和疫苗接种提供的免疫保护的演变了。细胞免疫在限制疾病严重程度和感染消退方面发挥着重要作用。SARS-CoV-2 特异性 T 细胞反应的早期出现、广度和强度与疾病严重程度相关,人们曾认为 T 细胞反应可能足以清除感染,使 COVID-19 患者中的 X 连锁或常染色体隐性无丙种球蛋白血症患者的疾病最小化。然而,我们对 CD8+细胞毒性淋巴细胞、CD4+辅助性 T 细胞、黏膜相关不变 T(MAIT)细胞和 CD4+滤泡辅助性 T(Tfh)细胞的表型和功能多样性的了解仍在不断发展,这些细胞在感染控制以及长期保护中发挥着关键作用。已经描述了 CD8+细胞毒性淋巴细胞如何通过分泌抗病毒细胞因子(IFN-γ 和 TNF-α)和直接杀死感染细胞来中断病毒复制,与疾病进展阶段呈负相关。此外,已经报道 CD4+辅助性 T 细胞是关键部分,可导致、协调并最终调节抗病毒免疫。例如,在一些更严重的 COVID-19 病例中,失调的 CD4+T 细胞特征可能导致更多促炎细胞因子的产生,从而导致致病性炎症。在这里,我们讨论了细胞免疫如何成为免疫系统其他组成部分围绕的轴心,因为它通过调节炎症级联反应,并因此调节先天免疫系统,以及通过 CD4+Tfh 细胞促进正确的体液反应,来协调和引导抗病毒反应。这篇综述还分析了细胞免疫在调节高亲和力中和抗体的产生以及生发中心 B 细胞分化为记忆和长寿命抗体分泌细胞中的关键作用。最后,由于目前有很高比例的接种人群,并且在某些情况下,甚至在某些国家正在接种疫苗加强针,我们还总结了针对细胞免疫反应对 SARS-CoV-2 的长期保护和交叉保护的较新方法。