Perm Federal Research Center, Institute of Ecology and Genetics of Microorganisms, Ural Branch of the Russian Academy of Sciences, Perm, 614081, Russia.
Biochemistry (Mosc). 2022 Jun;87(6):566-576. doi: 10.1134/S0006297922060086.
Despite numerous data on the absence or weak expression of the main functional receptor of SARS-CoV-2 angiotensin-converting enzyme 2 (ACE2) by T cells, it was recently demonstrated that the new coronavirus can efficiently infect T lymphocytes. Here, we analyze the data on the alternative (ACE2-independent) pathways of cell infection, identified T cell subpopulations that serve as the most plausible targets of SARS-CoV-2, discuss the mechanisms of virus-cell interaction, including both infectious and non-infectious pathways of T lymphocyte regulation, and estimate the role of the virus-dependent damage of T lymphocytes in COVID-19 pathogenesis. Particular attention is paid to regulatory T cells as potential targets of SARS-CoV-2, as well as to the possible involvement of exosomes in the sensitivity of peripheral T cells to the virus.
尽管有大量数据表明 T 细胞上 SARS-CoV-2 的主要功能受体血管紧张素转换酶 2(ACE2)缺失或表达较弱,但最近有研究表明,新型冠状病毒能够有效地感染 T 淋巴细胞。在这里,我们分析了细胞感染的替代(ACE2 非依赖性)途径的数据,确定了作为 SARS-CoV-2 最有可能的靶细胞亚群,讨论了病毒与细胞相互作用的机制,包括 T 淋巴细胞调节的感染性和非感染性途径,并估计了病毒依赖性 T 淋巴细胞损伤在 COVID-19 发病机制中的作用。特别关注调节性 T 细胞作为 SARS-CoV-2 的潜在靶点,以及外泌体在周围 T 细胞对病毒敏感性中的可能作用。