期刊
JOURNAL OF IMMUNOLOGY
卷 206, 期 11, 页码 2503-2507出版社
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.2100195
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资金
- University of Colorado School of Medicine
- National Institutes of Health, National Institute of Allergy and Infectious Diseases Grants [AI148919, AI066121, AI126899]
The use of human ACE2 protein-expressing mice to study SARS-CoV and SARS-CoV-2 has provided insights into the pathology of SARS-CoV-2 in mice, particularly in the C57BL/6 strain. By mapping CD8 T cell epitopes in immunized C57BL/6 mice, five major CD8 T cell epitopes were identified, including one common epitope between SARS-CoV and SARS-CoV-2. Further characterization of epitopes is necessary for detailed studies on T cell responses to vaccines and infection.
The prior existence of human ACE2 protein-expressing mice used to study SARS-CoV and the rapid development of mouse-adapted virus strains have allowed the study of SARS-CoV-2 in mice, even as we are still learning about its natural pathology in humans. With myriad genetically altered strains on the C57BL/6 background and the abundance of immunological reagents available to interrogate its immune responses, the C57BL/6 mice may provide useful insight into the immunology of SARS-CoV-2 infection and vaccination. To conduct more detailed studies on their T cell responses to vaccines and infection, the epitopes eliciting those responses must be characterized in further detail. In this study, we mapped CD8 T cell epitopes within the receptor binding domain of the SARS-CoV-2 spike protein in C57BL/6 mice. Our study identified five major CD8 T cell epitopes in immunized C57BL/6 mice, including one, VVLSFELL, presented by H-2K(b) and common between SARS-CoV and SARS-CoV-2.
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