Ontology highlight
ABSTRACT:
INSTRUMENT(S): Q Exactive
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): B Cell
SUBMITTER: Ravi Chand Bollineni
LAB HEAD: Johanna Olweus
PROVIDER: PXD028862 | Pride | 2023-03-11
REPOSITORIES: pride
Action | DRS | |||
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Peaks.zip | Other | |||
RB_200709_A01_EnvMembrane.raw | Raw | |||
RB_200709_A01_Nucleocapsid.raw | Raw | |||
RB_200709_A01_Spike.raw | Raw | |||
RB_200709_A01_Spike2_turncated.raw | Raw |
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Meyer Saskia S Blaas Isaac I Bollineni Ravi Chand RC Delic-Sarac Marina M Tran Trung T TT Knetter Cathrine C Dai Ke-Zheng KZ Madssen Torfinn Støve TS Vaage John T JT Gustavsen Alice A Yang Weiwen W Nissen-Meyer Lise Sofie Haug LSH Douvlataniotis Karolos K Laos Maarja M Nielsen Morten Milek MM Thiede Bernd B Søraas Arne A Lund-Johansen Fridtjof F Rustad Even H EH Olweus Johanna J
Cell reports 20230109 1
The emergence of SARS-CoV-2 variants of concern (VOC) is driven by mutations that mediate escape from neutralizing antibodies. There is also evidence that mutations can cause loss of T cell epitopes. However, studies on viral escape from T cell immunity have been hampered by uncertain estimates of epitope prevalence. Here, we map and quantify CD8 T cell responses to SARS-CoV-2-specific minimal epitopes in blood drawn from April to June 2020 from 83 COVID-19 convalescents. Among 37 HLA ligands el ...[more]