生物
NKG2D公司
细胞毒性T细胞
免疫学
白细胞介素21
免疫系统
主要组织相容性复合体
自然杀伤细胞
淋巴因子激活杀伤细胞
白细胞介素12
病毒学
T细胞
体外
生物化学
作者
Madeline Lee,Catherine A. Blish
出处
期刊:Nature Immunology
[Springer Nature]
日期:2023-07-17
卷期号:24 (10): 1628-1638
被引量:24
标识
DOI:10.1038/s41590-023-01560-8
摘要
Natural killer (NK) cells are critical effectors of antiviral immunity. Researchers have therefore sought to characterize the NK cell response to coronavirus disease 2019 (COVID-19) and the virus that causes it, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The NK cells of patients with severe COVID-19 undergo extensive phenotypic and functional changes. For example, the NK cells from critically ill patients with COVID-19 are highly activated and exhausted, with poor cytotoxic function and cytokine production upon stimulation. The NK cell response to SARS-CoV-2 is also modulated by changes induced in virally infected cells, including the ability of a viral peptide to bind HLA-E, preventing NK cells from receiving inhibitory signals, and the downregulation of major histocompatibility complex class I and ligands for the activating receptor NKG2D. These changes have important implications for the ability of infected cells to escape NK cell killing. The implications of these findings for antibody-dependent NK cell activity in COVID-19 are also reviewed. Despite these advances in the understanding of the NK cell response to SARS-CoV-2, there remain critical gaps in our current understanding and a wealth of avenues for future research on this topic. Blish and Lee review the response of natural killer cells to SARS-CoV-2 infection.
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