Single-cell transcriptome landscape and antigen receptor dynamic during SARS-CoV-2 vaccination
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Single-cell transcriptome landscape and antigen receptor dynamic during SARS-CoV-2 vaccination
Single-cell transcriptome landscape and antigen receptor dynamic during SARS-CoV-2 vaccination
Genes & Diseases2023年10卷第4期
作者机构:
1. State Key Laboratory of Agricultural Microbiology, College of Fisheries, Huazhong Agricultural University,Hubei,Wuhan,China,430072
2. State Key Laboratory of Virology, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences,Hubei,Wuhan,China,430071
3. State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University,Hubei,Wuhan,China,430072
4. Spatial FISH Co. Ltd.,Hubei,Jiangmen,China,529199
5. Department of Laboratory Medicine, Nanfang Hospital, Southern Medical University,Guangdong,Guangzhou,China,51015
6. Department of Transfusion Medicine, General Hospital of Central Theater Command,, Wuhan,Hubei,PLA,China,430070
7. Department of Laboratory Medicine, Maternal and Child Health Hospital of Hubei Province,Hubei,Wuhan,China,430070
Xiaojian Cao, Xiaohua Chen, Yaqi Zhu, et al. Single-cell transcriptome landscape and antigen receptor dynamic during SARS-CoV-2 vaccination[J]. Genes & Diseases, 2023,10(4). DOI: 10.1016/j.gendis.2022.08.020.
Single-cell transcriptome landscape and antigen receptor dynamic during SARS-CoV-2 vaccination
摘要
Abstract
Vaccination by inactivated vaccine is an effective strategy to prevent the COVID-19 pandemic. However
the detailed molecular immune response at single-cell level is poorly understood. In this study
we systematically delineated the landscape of the pre- and post-vaccination single-cell transcriptome
TCR (T cell antigen receptor) and BCR (B cell antigen receptor) expression profile of vaccinated candidates. The bulk TCR sequencing analysis of COVID-19 patients was also performed. Enrichment of a clonal CD8
+
T cell cluster expressing specific TCR was identified in both vaccination candidates and COVID-19 patients. These clonal CD8
+
T cells showed high expression of cytotoxicity
phagosome and antigen presentation related genes. The cell–cell interaction analysis revealed that monocytes and dendritic cells could interact with these cells and initiate phagocytosis via ICAM1-ITGAM and ITGB2 signaling. Together
our study systematically deciphered the detailed immunological response during SARS-CoV-2 vaccination and infection. It may facilitate understanding the immune response and the T-cell therapy against COVID-19.
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