biostudies-literatureTarke ANIAID NIH HHSNIH847-859.e11https://www.ebi.ac.uk/biostudies/studies/S-EPMC8784649biostudies-literatureUnknown185(5)We address whether T cell responses induced by different vaccine platforms (mRNA-1273, BNT162b2, Ad26.COV2.S, and NVX-CoV2373) cross-recognize early SARS-CoV-2 variants. T cell responses to early variants were preserved across vaccine platforms. By contrast, significant overall decreases were observed for memory B cells and neutralizing antibodies. In subjects ∼6 months post-vaccination, 90% (CD4⁺) and 87% (CD8⁺) of memory T cell responses were preserved against variants on average by AIM assay, and 84% (CD4⁺) and 85% (CD8⁺) preserved against Omicron. Omicron RBD memory B cell recognition was substantially reduced to 42% compared with other variants. T cell epitope repertoire analysis revealed a median of 11 and 10 spike epitopes recognized by CD4⁺ and CD8⁺ T cells, with average preservation > 80% for Omicron. Functional preservation of the majority of T cell responses may play an important role as a second-level defense against diverse variants.CellSARS-CoV-2 vaccination induces immunological T cell memory able to cross-recognize variants from Alpha to Omicron.PMC8784649R01 AI13519375N93021C00016P30 AI110527R25 AI147376U19 AI14274275N93019C00065Dan JMSette APhillips ETarke ASidney JGrifoni AMethot NGoodwin BWeiskopf DCoelho CHMallal SFilaci GCrotty SZhang Zda Silva Antunes RYu EDBloom NIfalseSARS-CoV-2 vaccination induces immunological T cell memory able to cross-recognize variants from Alpha to Omicron.We address whether T cell responses induced by different vaccine platforms (mRNA-1273, BNT162b2, Ad26.COV2.S, and NVX-CoV2373) cross-recognize early SARS-CoV-2 variants. T cell responses to early variants were preserved across vaccine platforms. By contrast, significant overall decreases were observed for memory B cells and neutralizing antibodies. In subjects ∼6 months post-vaccination, 90% (CD4⁺) and 87% (CD8⁺) of memory T cell responses were preserved against variants on average by AIM assay, and 84% (CD4⁺) and 85% (CD8⁺) preserved against Omicron. Omicron RBD memory B cell recognition was substantially reduced to 42% compared with other variants. T cell epitope repertoire analysis revealed a median of 11 and 10 spike epitopes recognized by CD4⁺ and CD8⁺ T cells, with average preservation > 80% for Omicron. Functional preservation of the majority of T cell responses may play an important role as a second-level defense against diverse variants.2022-01-01T00:00:00Z2022 Mar2026-05-31T01:01:00.101Z2025-04-04T23:29:35.285ZS-EPMC87846493513934010.1016/j.cell.2022.01.015