AUTHOR=Li Luo , Chen Qian , Han Xiaojian , Shen Meiying , Hu Chao , Chen Siyin , Zhang Jing , Wang Yingming , Li Tingting , Huang Jingjing , Li Shenglong , Hao Yanan , Jin Aishun 

TITLE=T Cell Immunity Evaluation and Immunodominant Epitope T Cell Receptor Identification of Severe Acute Respiratory Syndrome Coronavirus 2 Spike Glycoprotein in COVID-19 Convalescent Patients

JOURNAL=Frontiers in Cell and Developmental Biology

VOLUME=Volume 9 - 2021

YEAR=2021

URL=https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2021.696662

DOI=10.3389/fcell.2021.696662

ISSN=2296-634X

ABSTRACT=A better understanding of the role of T cells in the immune response to SARS-CoV-2 is helpful not only for vaccine development, but also for the treatment of COVID-19 patients. We used a matrix of overlapping peptides spanning the entire SARS-CoV-2 spike glycoprotein to study T cell responses from 8 COVID-19 convalescent patients. Although all participants exhibited SARS-CoV-2 T cell responses to multiple regions of S protein, the specific T cell response in the RBD region was the weakest. We identified 11 peptides containing CD4+ and /or CD8+ epitopes, and the frequency and epitopes of SARS-CoV-2-specific CD4+ T cells were higher. We isolated the SARS-CoV-2-specific CD4+ T cell receptors (TCRs) and inserted the TCRs into allogenic CD4+ T cells. These TCR-T cells can be activated by SARS-CoV-2 S peptide and produce IFN-γ in vitro. These results might provide valuable information for the development of vaccine and new therapies against COVID-19.