<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chi H</submitter><funding>Municipal Healthcare Joint-Innovation Major Project of Guangzhou</funding><funding>NIAID NIH HHS</funding><funding>National Institutes of Health</funding><funding>National Science and Technology Pillar Program</funding><funding>State Key Laboratory of Respiratory Disease</funding><pagination>2069-2075</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5411280</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>35(16)</volume><pubmed_abstract>The Middle East respiratory syndrome coronavirus (MERS-CoV), is an emerging pathogen that continues to cause outbreaks in the Arabian peninsula and in travelers from this region, raising the concern that a global pandemic could occur. Here, we show that a DNA vaccine encoding the first 725 amino acids (S1) of MERS-CoV spike (S) protein induces antigen-specific humoral and cellular immune responses in mice. With three immunizations, high titers of neutralizing antibodies (up to 1: 10&lt;sup>4&lt;/sup>) were generated without adjuvant. DNA vaccination with the MERS-CoV S1 gene markedly increased the frequencies of antigen-specific CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> T cells secreting IFN-γ and other cytokines. Both pcDNA3.1-S1 DNA vaccine immunization and passive transfer of immune serum from pcDNA3.1-S1 vaccinated mice protected Ad5-hDPP4-transduced mice from MERS-CoV challenge. These results demonstrate that a DNA vaccine encoding MERS-CoV S1 protein induces strong protective immune responses against MERS-CoV infection.</pubmed_abstract><journal>Vaccine</journal><pubmed_title>DNA vaccine encoding Middle East respiratory syndrome coronavirus S1 protein induces protective immune responses in mice.</pubmed_title><pmcid>PMC5411280</pmcid><funding_grant_id>2014SKRD-001</funding_grant_id><funding_grant_id>R01 AI129269</funding_grant_id><funding_grant_id>RO1 AI091322</funding_grant_id><funding_grant_id>201604020011</funding_grant_id><funding_grant_id>2013BAD12B04</funding_grant_id><funding_grant_id>R01 AI091322</funding_grant_id><funding_grant_id>PO1 AI060699</funding_grant_id><funding_grant_id>P01 AI060699</funding_grant_id><pubmed_authors>Gai W</pubmed_authors><pubmed_authors>Xia X</pubmed_authors><pubmed_authors>Zheng X</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Perlman S</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Chi H</pubmed_authors><pubmed_authors>Yang S</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors></additional><is_claimable>false</is_claimable><name>DNA vaccine encoding Middle East respiratory syndrome coronavirus S1 protein induces protective immune responses in mice.</name><description>The Middle East respiratory syndrome coronavirus (MERS-CoV), is an emerging pathogen that continues to cause outbreaks in the Arabian peninsula and in travelers from this region, raising the concern that a global pandemic could occur. Here, we show that a DNA vaccine encoding the first 725 amino acids (S1) of MERS-CoV spike (S) protein induces antigen-specific humoral and cellular immune responses in mice. With three immunizations, high titers of neutralizing antibodies (up to 1: 10&lt;sup>4&lt;/sup>) were generated without adjuvant. DNA vaccination with the MERS-CoV S1 gene markedly increased the frequencies of antigen-specific CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> T cells secreting IFN-γ and other cytokines. Both pcDNA3.1-S1 DNA vaccine immunization and passive transfer of immune serum from pcDNA3.1-S1 vaccinated mice protected Ad5-hDPP4-transduced mice from MERS-CoV challenge. These results demonstrate that a DNA vaccine encoding MERS-CoV S1 protein induces strong protective immune responses against MERS-CoV infection.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Apr</publication><modification>2024-11-06T13:15:28.483Z</modification><creation>2019-03-26T23:27:45Z</creation></dates><accession>S-EPMC5411280</accession><cross_references><pubmed>28314561</pubmed><doi>10.1016/j.vaccine.2017.02.063</doi></cross_references></HashMap>