SARS-CoV-2-specific T cells in unexposed adults display broad trafficking potential and cross-react with commensal antigens.

SARS-CoV-2-specific T cells in unexposed adults display broad trafficking potential and cross-react with commensal antigens.
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DOI:
10.1126/sciimmunol.abn3127
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发表时间:
2022-10-21
期刊:
影响因子:
24.8
通讯作者:
Su, Laura F.
Su, Laura F.
中科院分区:
医学1区
文献类型:
--
作者:
Bartolo, Laurent;Afroz, Sumbul;Pan, Yi-Gen;Xu, Ruozhang;Williams, Lea;Lin, Chin-Fang;Tanes, Ceylan;Bittinger, Kyle;Friedman, Elliot S.;Gimotty, Phyllis A.;Wu, Gary D.;Su, Laura F.

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The baseline composition of T cells directly impacts later response to pathogens, but the complexity of precursor states remains poorly defined. Here, we examined the baseline state of SARS-CoV-2-specific T cells in unexposed individuals. SARS-CoV-2-specific CD4+ T cells were identified in pre-pandemic blood samples by class II peptide-MHC tetramer staining and enrichment. Our data revealed a substantial number of SARS-CoV-2-specific T cells that expressed memory phenotype markers. Integrated phenotypic analyses demonstrated diverse pre-existing memory states that included cells with distinct polarization states and trafficking potential to barrier tissues. T cell clones generated from tetramer-labeled cells cross-reacted with antigens from commensal bacteria in the skin and gastrointestinal tract. Direct ex vivo tetramer staining for one spike-specific population showed a similar level of cross-reactivity to sequences from endemic coronavirus and commensal bacteria. These data highlight the complexity of precursor T cell repertoire and implicate non-infectious exposures to common microbes as a key factor that shapes human pre-existing immunity to SARS-CoV-2. Pre-existing immunity to SARS-CoV-2 displayed diverse phenotypes, had broad tissue tropism and cross-reacted with commensal antigens.
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