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Cell Rep ; 35(8): 109179, 2021 05 25.
Article in English | MEDLINE | ID: covidwho-1230394

ABSTRACT

Understanding and eliciting protective immune responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an urgent priority. To facilitate these objectives, we profile the repertoire of human leukocyte antigen class II (HLA-II)-bound peptides presented by HLA-DR diverse monocyte-derived dendritic cells pulsed with SARS-CoV-2 spike (S) protein. We identify 209 unique HLA-II-bound peptide sequences, many forming nested sets, which map to sites throughout S including glycosylated regions. Comparison of the glycosylation profile of the S protein to that of the HLA-II-bound S peptides reveals substantial trimming of glycan residues on the latter, likely induced during antigen processing. Our data also highlight the receptor-binding motif in S1 as a HLA-DR-binding peptide-rich region and identify S2-derived peptides with potential for targeting by cross-protective vaccine-elicited responses. Results from this study will aid analysis of CD4+ T cell responses in infected individuals and vaccine recipients and have application in next-generation vaccine design.


Subject(s)
COVID-19/immunology , Dendritic Cells/immunology , Histocompatibility Antigens Class II/immunology , Peptides/immunology , Spike Glycoprotein, Coronavirus/immunology , Amino Acid Sequence , Antigen Presentation , COVID-19/virology , Epitope Mapping , Epitopes, T-Lymphocyte/immunology , Glycosylation , Humans , Protein Binding , Protein Interaction Domains and Motifs , SARS-CoV-2/immunology , T-Lymphocytes/immunology
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