<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang H</submitter><funding>Excellent Young Scientist Program of the National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China</funding><funding>Research Units of Adaptive Evolution and Control of Emerging Viruses, Chinese Academy of Medical Sciences</funding><pagination>2332</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9696057</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(11)</volume><pubmed_abstract>Zika virus (ZIKV)-specific T cells are activated by different peptides derived from virus structural and nonstructural proteins, and contributed to the viral clearance or protective immunity. Herein, we have depicted the profile of CD8+ and CD4+ T cell immunogenicity of ZIKV proteins in C57BL/6 (H-2&lt;sup>b&lt;/sup>) and BALB/c (H-2&lt;sup>d&lt;/sup>) mice, and found that featured cellular immunity antigens were variant among different murine alleles. In H-2&lt;sup>b&lt;/sup> mice, the proteins E, NS2, NS3 and NS5 are recognized as immunodominant antigens by CD8+ T cells, while NS4 is dominantly recognized by CD4+ T cells. In contrast, in H-2&lt;sup>d&lt;/sup> mice, NS1 and NS4 are the dominant CD8+ T cell antigen and NS4 as the dominant CD4+ T cell antigen, respectively. Among the synthesized 364 overlapping po</pubmed_abstract><journal>Viruses</journal><pubmed_title>The CD8+ and CD4+ T Cell Immunogen Atlas of Zika Virus Reveals E, NS1 and NS4 Proteins as the Vaccine Targets.</pubmed_title><pmcid>PMC9696057</pmcid><funding_grant_id>2018RU009</funding_grant_id><funding_grant_id>81822040</funding_grant_id><funding_grant_id>82161148008</funding_grant_id><funding_grant_id>81971501</funding_grant_id><pubmed_authors>Zhang F</pubmed_authors><pubmed_authors>Peng W</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Lu X</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Ye B</pubmed_authors><pubmed_authors>Liu P</pubmed_authors><pubmed_authors>Xiao W</pubmed_authors><pubmed_authors>Lu D</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Wu G</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors><pubmed_authors>Shu L</pubmed_authors><pubmed_authors>Zhao M</pubmed_authors><pubmed_authors>Wang P</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Liu WJ</pubmed_authors><pubmed_authors>Lu S</pubmed_authors><pubmed_authors>Tan S</pubmed_authors><pubmed_authors>Zong K</pubmed_authors><pubmed_authors>Gao GF</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>The CD8+ and CD4+ T Cell Immunogen Atlas of Zika Virus Reveals E, NS1 and NS4 Proteins as the Vaccine Targets.</name><description>Zika virus (ZIKV)-specific T cells are activated by different peptides derived from virus structural and nonstructural proteins, and contributed to the viral clearance or protective immunity. Herein, we have depicted the profile of CD8+ and CD4+ T cell immunogenicity of ZIKV proteins in C57BL/6 (H-2&lt;sup>b&lt;/sup>) and BALB/c (H-2&lt;sup>d&lt;/sup>) mice, and found that featured cellular immunity antigens were variant among different murine alleles. In H-2&lt;sup>b&lt;/sup> mice, the proteins E, NS2, NS3 and NS5 are recognized as immunodominant antigens by CD8+ T cells, while NS4 is dominantly recognized by CD4+ T cells. In contrast, in H-2&lt;sup>d&lt;/sup> mice, NS1 and NS4 are the dominant CD8+ T cell antigen and NS4 as the dominant CD4+ T cell antigen, respectively. Among the synthesized 364 overlapping po</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-05-10T03:13:23.05Z</modification><creation>2024-11-07T00:33:44.193Z</creation></dates><accession>S-EPMC9696057</accession><cross_references><pubmed>36366430</pubmed><doi>10.3390/v14112332</doi></cross_references></HashMap>