<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(1)</volume><submitter>Wang J</submitter><pubmed_abstract>The effects of different SARS-CoV-2 vaccinations and variant infection histories on imprinting population immunity and their influence on emerging escape mutants remain unclear. We found that Omicron (BA.1) breakthrough infection, regardless of vaccination with two-dose mRNA vaccines (M-M-o) or two-dose inactivated vaccines (I-I-o), led to higher neutralizing antibody levels against different variants and stronger T-cell responses than Delta breakthrough infection after two-dose inactivated vaccine vaccination (I-I-δ). Furthermore, different vaccination-infection patterns imprinted virus-specific T-cell differentiation; M-M-ο showed higher S/M/N/E-specific CD4+ T cells and less portion of virus-specific CD45RA+CD27-CD8+ T cells by ex vivo assay. Breakthrough infection groups showed higher </pubmed_abstract><journal>Cell discovery</journal><pagination>136</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9769462</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>SARS-CoV-2 vaccination-infection pattern imprints and diversifies T cell differentiation and neutralizing response against Omicron subvariants.</pubmed_title><pmcid>PMC9769462</pmcid><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Zhong N</pubmed_authors><pubmed_authors>Luo Q</pubmed_authors><pubmed_authors>Wei R</pubmed_authors><pubmed_authors>Mei X</pubmed_authors><pubmed_authors>Cao J</pubmed_authors><pubmed_authors>Li K</pubmed_authors><pubmed_authors>Zhong J</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Zhao Z</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Huang P</pubmed_authors></additional><is_claimable>false</is_claimable><name>SARS-CoV-2 vaccination-infection pattern imprints and diversifies T cell differentiation and neutralizing response against Omicron subvariants.</name><description>The effects of different SARS-CoV-2 vaccinations and variant infection histories on imprinting population immunity and their influence on emerging escape mutants remain unclear. We found that Omicron (BA.1) breakthrough infection, regardless of vaccination with two-dose mRNA vaccines (M-M-o) or two-dose inactivated vaccines (I-I-o), led to higher neutralizing antibody levels against different variants and stronger T-cell responses than Delta breakthrough infection after two-dose inactivated vaccine vaccination (I-I-δ). Furthermore, different vaccination-infection patterns imprinted virus-specific T-cell differentiation; M-M-ο showed higher S/M/N/E-specific CD4+ T cells and less portion of virus-specific CD45RA+CD27-CD8+ T cells by ex vivo assay. Breakthrough infection groups showed higher </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-26T00:40:09.028Z</modification><creation>2025-04-06T09:50:47.102Z</creation></dates><accession>S-EPMC9769462</accession><cross_references><pubmed>36543767</pubmed><doi>10.1038/s41421-022-00501-3</doi></cross_references></HashMap>