Serveur d'exploration MERS

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A Highly Immunogenic, Protective, and Safe Adenovirus-Based Vaccine Expressing Middle East Respiratory Syndrome Coronavirus S1-CD40L Fusion Protein in a Transgenic Human Dipeptidyl Peptidase 4 Mouse Model.

Identifieur interne : 000596 ( PubMed/Curation ); précédent : 000595; suivant : 000597

A Highly Immunogenic, Protective, and Safe Adenovirus-Based Vaccine Expressing Middle East Respiratory Syndrome Coronavirus S1-CD40L Fusion Protein in a Transgenic Human Dipeptidyl Peptidase 4 Mouse Model.

Auteurs : Anwar M. Hashem ; Abdullah Algaissi ; Anurodh Shankar Agrawal ; Sawsan S. Al-Amri [Arabie saoudite] ; Rowa Y. Alhabbab [Arabie saoudite] ; Sayed S. Sohrab [Arabie saoudite] ; Abdulrahman S Almasoud [Arabie saoudite] ; Naif Khalaf Alharbi [Arabie saoudite] ; Bi-Hung Peng ; Marsha Russell [Canada] ; Xuguang Li [Canada] ; Chien-Te K. Tseng

Source :

RBID : pubmed:30911758

Abstract

Infection control measures have played a major role in limiting human/camel-to-human transmission of Middle East respiratory syndrome coronavirus (MERS-CoV); however, development of effective and safe human or camel vaccines is warranted.

DOI: 10.1093/infdis/jiz137
PubMed: 30911758

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pubmed:30911758

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Anwar M. Hashem
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Abdullah Algaissi
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<nlm:affiliation>Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston.</nlm:affiliation>
<wicri:noCountry code="subField">Galveston</wicri:noCountry>
</affiliation>
Anurodh Shankar Agrawal
<affiliation>
<nlm:affiliation>Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston.</nlm:affiliation>
<wicri:noCountry code="subField">Galveston</wicri:noCountry>
</affiliation>
Bi-Hung Peng
<affiliation>
<nlm:affiliation>Department of Neurosciences, Cell Biology, and Anatomy, University of Texas Medical Branch, Galveston.</nlm:affiliation>
<wicri:noCountry code="subField">Galveston</wicri:noCountry>
</affiliation>
Chien-Te K. Tseng
<affiliation>
<nlm:affiliation>Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston.</nlm:affiliation>
<wicri:noCountry code="subField">Galveston</wicri:noCountry>
</affiliation>

Le document en format XML

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<name sortKey="S Almasoud, Abdulrahman" sort="S Almasoud, Abdulrahman" uniqKey="S Almasoud A" first="Abdulrahman" last="S Almasoud">Abdulrahman S Almasoud</name>
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<name sortKey="Alharbi, Naif Khalaf" sort="Alharbi, Naif Khalaf" uniqKey="Alharbi N" first="Naif Khalaf" last="Alharbi">Naif Khalaf Alharbi</name>
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<nlm:affiliation>Department of Infectious Disease Research, King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.</nlm:affiliation>
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<name sortKey="Peng, Bi Hung" sort="Peng, Bi Hung" uniqKey="Peng B" first="Bi-Hung" last="Peng">Bi-Hung Peng</name>
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<wicri:noCountry code="subField">Galveston</wicri:noCountry>
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<name sortKey="Russell, Marsha" sort="Russell, Marsha" uniqKey="Russell M" first="Marsha" last="Russell">Marsha Russell</name>
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<nlm:affiliation>Center for Vaccine Evaluation, Biologics and Genetic Therapies Directorate, Health Canada, Ottawa, Ontario.</nlm:affiliation>
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<name sortKey="Li, Xuguang" sort="Li, Xuguang" uniqKey="Li X" first="Xuguang" last="Li">Xuguang Li</name>
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<nlm:affiliation>Center for Vaccine Evaluation, Biologics and Genetic Therapies Directorate, Health Canada, Ottawa, Ontario.</nlm:affiliation>
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<name sortKey="Tseng, Chien Te K" sort="Tseng, Chien Te K" uniqKey="Tseng C" first="Chien-Te K" last="Tseng">Chien-Te K. Tseng</name>
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<title level="j">The Journal of infectious diseases</title>
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<div type="abstract" xml:lang="en">Infection control measures have played a major role in limiting human/camel-to-human transmission of Middle East respiratory syndrome coronavirus (MERS-CoV); however, development of effective and safe human or camel vaccines is warranted.</div>
</front>
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<PMID Version="1">30911758</PMID>
<DateRevised>
<Year>2020</Year>
<Month>04</Month>
<Day>03</Day>
</DateRevised>
<Article PubModel="Print">
<Journal>
<ISSN IssnType="Electronic">1537-6613</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>220</Volume>
<Issue>10</Issue>
<PubDate>
<Year>2019</Year>
<Month>Oct</Month>
<Day>08</Day>
</PubDate>
</JournalIssue>
<Title>The Journal of infectious diseases</Title>
<ISOAbbreviation>J. Infect. Dis.</ISOAbbreviation>
</Journal>
<ArticleTitle>A Highly Immunogenic, Protective, and Safe Adenovirus-Based Vaccine Expressing Middle East Respiratory Syndrome Coronavirus S1-CD40L Fusion Protein in a Transgenic Human Dipeptidyl Peptidase 4 Mouse Model.</ArticleTitle>
<Pagination>
<MedlinePgn>1558-1567</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1093/infdis/jiz137</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Infection control measures have played a major role in limiting human/camel-to-human transmission of Middle East respiratory syndrome coronavirus (MERS-CoV); however, development of effective and safe human or camel vaccines is warranted.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We extended and optimized our previous recombinant adenovirus 5 (rAd5)-based vaccine platform characterized by in vivo amplified and CD40-mediated specific responses to generate MERS-CoV S1 subunit-based vaccine. We generated rAd5 constructs expressing CD40-targeted S1 fusion protein (rAd5-S1/F/CD40L), untargeted S1 (rAd5-S1), and Green Fluorescent Protein (rAd5-GFP), and evaluated their efficacy and safety in human dipeptidyl peptidase 4 transgenic (hDPP4 Tg+) mice.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Immunization of hDPP4 Tg+ mice with a single dose of rAd5-S1/F/CD40L elicited as robust and significant specific immunoglobulin G and neutralizing antibodies as those induced with 2 doses of rAd5-S1. After MERS-CoV challenge, both vaccines conferred complete protection against morbidity and mortality, as evidenced by significantly undetectable/reduced pulmonary viral loads compared to the control group. However, rAd5-S1- but not rAd5-S1/F/CD40L-immunized mice exhibited marked pulmonary perivascular hemorrhage post-MERS-CoV challenge despite the observed protection.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Incorporation of CD40L into rAd5-based MERS-CoV S1 vaccine targeting molecule and molecular adjuvants not only enhances immunogenicity and efficacy but also prevents inadvertent pulmonary pathology after viral challenge, thereby offering a promising strategy to enhance safety and potency of vaccines.</AbstractText>
<CopyrightInformation>© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.</CopyrightInformation>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Medical Laboratories Technology, College of Applied Medical Sciences, Jazan University.</Affiliation>
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</AffiliationInfo>
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<AffiliationInfo>
<Affiliation>Special Infectious Agents Unit, King Fahd Medical Research Center, King Abdulaziz University, Jeddah, Saudi Arabia.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah.</Affiliation>
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<LastName>S Almasoud</LastName>
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</AffiliationInfo>
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</AffiliationInfo>
</Author>
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<LastName>Peng</LastName>
<ForeName>Bi-Hung</ForeName>
<Initials>BH</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurosciences, Cell Biology, and Anatomy, University of Texas Medical Branch, Galveston.</Affiliation>
</AffiliationInfo>
</Author>
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<ForeName>Marsha</ForeName>
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<Affiliation>Center for Vaccine Evaluation, Biologics and Genetic Therapies Directorate, Health Canada, Ottawa, Ontario.</Affiliation>
</AffiliationInfo>
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<LastName>Li</LastName>
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<AffiliationInfo>
<Affiliation>Center for Vaccine Evaluation, Biologics and Genetic Therapies Directorate, Health Canada, Ottawa, Ontario.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Tseng</LastName>
<ForeName>Chien-Te K</ForeName>
<Initials>CK</Initials>
<AffiliationInfo>
<Affiliation>Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Center of Biodefense and Emerging Disease, University of Texas Medical Branch, Galveston.</Affiliation>
</AffiliationInfo>
</Author>
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<Language>eng</Language>
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<Country>United States</Country>
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<ISSNLinking>0022-1899</ISSNLinking>
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<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">CD40L</Keyword>
<Keyword MajorTopicYN="N">MERS-CoV</Keyword>
<Keyword MajorTopicYN="N">adenovirus</Keyword>
<Keyword MajorTopicYN="N">immunopathology</Keyword>
<Keyword MajorTopicYN="N">vaccine</Keyword>
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