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前沿:SARS-CoV-2 引发的肺部驻留 T 细胞不能介导对二次感染的保护。

Cutting Edge: Lung-Resident T Cells Elicited by SARS-CoV-2 Do Not Mediate Protection against Secondary Infection.

机构信息

Immunity to Pulmonary Pathogens Section, Laboratory of Bacteriology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT.

Immunity to Pulmonary Pathogens Section, Laboratory of Bacteriology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT

出版信息

J Immunol. 2021 Nov 15;207(10):2399-2404. doi: 10.4049/jimmunol.2100608. Epub 2021 Oct 4.

Abstract

Immunity to pulmonary infection typically requires elicitation of lung-resident T cells that subsequently confer protection against secondary infection. The presence of tissue-resident T cells in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) convalescent patients is unknown. Using a sublethal mouse model of coronavirus disease 2019, we determined if SARS-CoV-2 infection potentiated Ag-specific pulmonary resident CD4 and CD8 T cell responses and if these cells mediated protection against secondary infection. S protein-specific T cells were present in resident and circulating populations. However, M and N protein-specific T cells were detected only in the resident T cell pool. Using an adoptive transfer strategy, we found that T cells from SARS-CoV-2 immune animals did not protect naive mice. These data indicate that resident T cells are elicited by SARS-CoV-2 infection but are not sufficient for protective immunity.

摘要

针对肺部感染的免疫通常需要诱导肺驻留 T 细胞,随后这些细胞可提供针对二次感染的保护。严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 康复患者中是否存在组织驻留 T 细胞尚不清楚。我们使用亚致死性的 2019 年冠状病毒病小鼠模型,确定 SARS-CoV-2 感染是否增强了针对抗原的肺驻留 CD4 和 CD8 T 细胞反应,以及这些细胞是否介导对二次感染的保护。S 蛋白特异性 T 细胞存在于驻留和循环群体中。然而,M 和 N 蛋白特异性 T 细胞仅在驻留 T 细胞池中检测到。通过过继转移策略,我们发现来自 SARS-CoV-2 免疫动物的 T 细胞不能保护未感染的小鼠。这些数据表明,SARS-CoV-2 感染会引发驻留 T 细胞反应,但不足以产生保护性免疫。

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