作者
Thi HO Nguyen, Louise C Rowntree, Jan Petersen, Brendon Y Chua, Luca Hensen, Lukasz Kedzierski, Carolien E van de Sandt, Priyanka Chaurasia, Hyon-Xhi Tan, Jennifer R Habel, Wuji Zhang, Lilith F Allen, Linda Earnest, Kai Yan Mak, Jennifer A Juno, Kathleen Wragg, Francesca L Mordant, Fatima Amanat, Florian Krammer, Nicole A Mifsud, Denise L Doolan, Katie L Flanagan, Sabrina Sonda, Jasveen Kaur, Linda M Wakim, Glen P Westall, Fiona James, Effie Mouhtouris, Claire L Gordon, Natasha E Holmes, Olivia C Smibert, Jason A Trubiano, Allen C Cheng, Peter Harcourt, Patrick Clifton, Jeremy Chase Crawford, Paul G Thomas, Adam K Wheatley, Stephen J Kent, Jamie Rossjohn, Joseph Torresi, Katherine Kedzierska
发表日期
2021/5/11
期刊
Immunity
卷号
54
期号
5
页码范围
1066-1082. e5
出版商
Elsevier
简介
To better understand primary and recall T cell responses during coronavirus disease 2019 (COVID-19), it is important to examine unmanipulated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-specific T cells. By using peptide-human leukocyte antigen (HLA) tetramers for direct ex vivo analysis, we characterized CD8+ T cells specific for SARS-CoV-2 epitopes in COVID-19 patients and unexposed individuals. Unlike CD8+ T cells directed toward subdominant epitopes (B7/N257, A2/S269, and A24/S1,208) CD8+ T cells specific for the immunodominant B7/N105 epitope were detected at high frequencies in pre-pandemic samples and at increased frequencies during acute COVID-19 and convalescence. SARS-CoV-2-specific CD8+ T cells in pre-pandemic samples from children, adults, and elderly individuals predominantly displayed a naive phenotype, indicating a lack of previous cross-reactive …
引用总数
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