<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(6)</volume><submitter>Zhang J</submitter><pubmed_abstract>The individual HLA-related susceptibility to emerging viral diseases such as COVID-19 underscores the importance of understanding how HLA polymorphism influences peptide presentation and T cell recognition. Similar to HLA-A*0101, which is one of the earliest identified HLA alleles among the human population, HLA-A*2601 possesses a similar characteristic for the binding peptide and acts as a prevalent allomorph in HLA-I. In this study, we found that, compared with HLA-A*0101, HLA-A*2601 individuals exhibit distinctive features for the T cell responses to SARS-CoV-2 and influenza virus after infection and/or vaccination. The heterogeneous T cell responses can be attributed to the distinct preference of HLA-A*2601 and HLA-A*0101 to T cell epitope motifs with negative-charged residues at the P</pubmed_abstract><journal>ImmunoHorizons</journal><pagination>415-430</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11220742</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Uncommon P1 Anchor-featured Viral T Cell Epitope Preference within HLA-A*2601 and HLA-A*0101 Individuals.</pubmed_title><pmcid>PMC11220742</pmcid><pubmed_authors>Tian J</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Zhang D</pubmed_authors><pubmed_authors>Qi J</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Guo Y</pubmed_authors><pubmed_authors>Ye B</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Sun Z</pubmed_authors><pubmed_authors>Yue C</pubmed_authors><pubmed_authors>Gao GF</pubmed_authors><pubmed_authors>Chai Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Uncommon P1 Anchor-featured Viral T Cell Epitope Preference within HLA-A*2601 and HLA-A*0101 Individuals.</name><description>The individual HLA-related susceptibility to emerging viral diseases such as COVID-19 underscores the importance of understanding how HLA polymorphism influences peptide presentation and T cell recognition. Similar to HLA-A*0101, which is one of the earliest identified HLA alleles among the human population, HLA-A*2601 possesses a similar characteristic for the binding peptide and acts as a prevalent allomorph in HLA-I. In this study, we found that, compared with HLA-A*0101, HLA-A*2601 individuals exhibit distinctive features for the T cell responses to SARS-CoV-2 and influenza virus after infection and/or vaccination. The heterogeneous T cell responses can be attributed to the distinct preference of HLA-A*2601 and HLA-A*0101 to T cell epitope motifs with negative-charged residues at the P</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2026-06-02T21:20:09.587Z</modification><creation>2025-04-04T12:22:12.057Z</creation></dates><accession>S-EPMC11220742</accession><cross_references><pubmed>38885041</pubmed><doi>10.4049/immunohorizons.2400026</doi></cross_references></HashMap>