CD8+ T Cells Responding to the Middle East Respiratory Syndrome Coronavirus Nucleocapsid Protein Delivered by Vaccinia Virus MVA in Mice
Identifieur interne : 000A49 ( Main/Exploration ); précédent : 000A48; suivant : 000A50CD8+ T Cells Responding to the Middle East Respiratory Syndrome Coronavirus Nucleocapsid Protein Delivered by Vaccinia Virus MVA in Mice
Auteurs : Svenja Veit ; Sylvia Jany ; Robert Fux ; Gerd Sutter [Allemagne] ; Asisa Volz [Allemagne]Source :
- Viruses [ 1999-4915 ] ; 2018.
Descripteurs français
- KwdFr :
- Animaux, Anticorps antiviraux (immunologie), Anticorps neutralisants (immunologie), Coronavirus du syndrome respiratoire du Moyen-Orient (immunologie), Déterminants antigéniques des lymphocytes T (immunologie), Femelle, Immunité cellulaire, Infections à coronavirus (immunologie), Lymphocytes T CD8+ (immunologie), Protéines nucléocapside (génétique), Protéines nucléocapside (immunologie), Protéines recombinantes (immunologie), Souris, Souris de lignée BALB C, Vaccination, Vaccins antiviraux (immunologie), Virus de la vaccine (génétique), Virus de la vaccine (immunologie).
- MESH :
- génétique : Protéines nucléocapside, Virus de la vaccine.
- immunologie : Anticorps antiviraux, Anticorps neutralisants, Coronavirus du syndrome respiratoire du Moyen-Orient, Déterminants antigéniques des lymphocytes T, Infections à coronavirus, Lymphocytes T CD8+, Protéines nucléocapside, Protéines recombinantes, Vaccins antiviraux, Virus de la vaccine.
- Animaux, Femelle, Immunité cellulaire, Souris, Souris de lignée BALB C, Vaccination.
English descriptors
- KwdEn :
- Animals, Antibodies, Neutralizing (immunology), Antibodies, Viral (immunology), CD8-Positive T-Lymphocytes (immunology), Coronavirus Infections (immunology), Epitopes, T-Lymphocyte (immunology), Female, Immunity, Cellular, Mice, Mice, Inbred BALB C, Middle East Respiratory Syndrome Coronavirus (immunology), Nucleocapsid Proteins (genetics), Nucleocapsid Proteins (immunology), Recombinant Proteins (immunology), Vaccination, Vaccinia virus (genetics), Vaccinia virus (immunology), Viral Vaccines (immunology).
- MESH :
- chemical , genetics : Nucleocapsid Proteins.
- chemical , immunology : Antibodies, Neutralizing, Antibodies, Viral, Epitopes, T-Lymphocyte, Nucleocapsid Proteins, Recombinant Proteins, Viral Vaccines.
- genetics : Vaccinia virus.
- immunology : CD8-Positive T-Lymphocytes, Coronavirus Infections, Middle East Respiratory Syndrome Coronavirus, Vaccinia virus.
- Animals, Female, Immunity, Cellular, Mice, Mice, Inbred BALB C, Vaccination.
Abstract
Middle East respiratory syndrome coronavirus (MERS-CoV), a novel infectious agent causing severe respiratory disease and death in humans, was first described in 2012. Antibodies directed against the MERS-CoV spike (S) protein are thought to play a major role in controlling MERS-CoV infection and in mediating vaccine-induced protective immunity. In contrast, relatively little is known about the role of T cell responses and the antigenic targets of MERS-CoV that are recognized by CD8+ T cells. In this study, the highly conserved MERS-CoV nucleocapsid (N) protein served as a target immunogen to elicit MERS-CoV-specific cellular immune responses. Modified Vaccinia virus Ankara (MVA), a safety-tested strain of vaccinia virus for preclinical and clinical vaccine research, was used for generating MVA-MERS-N expressing recombinant N protein. Overlapping peptides spanning the whole MERS-CoV N polypeptide were used to identify major histocompatibility complex class I/II-restricted T cell responses in BALB/c mice immunized with MVA-MERS-N. We have identified a H2-d restricted decamer peptide epitope in the MERS-N protein with CD8+ T cell antigenicity. The identification of this epitope, and the availability of the MVA-MERS-N candidate vaccine, will help to evaluate MERS-N-specific immune responses and the potential immune correlates of vaccine-mediated protection in the appropriate murine models of MERS-CoV infection.
Url:
DOI: 10.3390/v10120718
PubMed: 30558354
PubMed Central: 6316859
Affiliations:
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Le document en format XML
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<term>Antibodies, Neutralizing (immunology)</term>
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<term>CD8-Positive T-Lymphocytes (immunology)</term>
<term>Coronavirus Infections (immunology)</term>
<term>Epitopes, T-Lymphocyte (immunology)</term>
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<term>Nucleocapsid Proteins (immunology)</term>
<term>Recombinant Proteins (immunology)</term>
<term>Vaccination</term>
<term>Vaccinia virus (genetics)</term>
<term>Vaccinia virus (immunology)</term>
<term>Viral Vaccines (immunology)</term>
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<term>Anticorps antiviraux (immunologie)</term>
<term>Anticorps neutralisants (immunologie)</term>
<term>Coronavirus du syndrome respiratoire du Moyen-Orient (immunologie)</term>
<term>Déterminants antigéniques des lymphocytes T (immunologie)</term>
<term>Femelle</term>
<term>Immunité cellulaire</term>
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<term>Nucleocapsid Proteins</term>
<term>Recombinant Proteins</term>
<term>Viral Vaccines</term>
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<front><div type="abstract" xml:lang="en"><p>Middle East respiratory syndrome coronavirus (MERS-CoV), a novel infectious agent causing severe respiratory disease and death in humans, was first described in 2012. Antibodies directed against the MERS-CoV spike (S) protein are thought to play a major role in controlling MERS-CoV infection and in mediating vaccine-induced protective immunity. In contrast, relatively little is known about the role of T cell responses and the antigenic targets of MERS-CoV that are recognized by CD8+ T cells. In this study, the highly conserved MERS-CoV nucleocapsid (N) protein served as a target immunogen to elicit MERS-CoV-specific cellular immune responses. Modified Vaccinia virus Ankara (MVA), a safety-tested strain of vaccinia virus for preclinical and clinical vaccine research, was used for generating MVA-MERS-N expressing recombinant N protein. Overlapping peptides spanning the whole MERS-CoV N polypeptide were used to identify major histocompatibility complex class I/II-restricted T cell responses in BALB/c mice immunized with MVA-MERS-N. We have identified a H2-d restricted decamer peptide epitope in the MERS-N protein with CD8+ T cell antigenicity. The identification of this epitope, and the availability of the MVA-MERS-N candidate vaccine, will help to evaluate MERS-N-specific immune responses and the potential immune correlates of vaccine-mediated protection in the appropriate murine models of MERS-CoV infection.</p>
</div>
</front>
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</TEI>
<affiliations><list><country><li>Allemagne</li>
</country>
<region><li>Bavière</li>
<li>District de Haute-Bavière</li>
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<settlement><li>Munich</li>
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<tree><noCountry><name sortKey="Fux, Robert" sort="Fux, Robert" uniqKey="Fux R" first="Robert" last="Fux">Robert Fux</name>
<name sortKey="Jany, Sylvia" sort="Jany, Sylvia" uniqKey="Jany S" first="Sylvia" last="Jany">Sylvia Jany</name>
<name sortKey="Veit, Svenja" sort="Veit, Svenja" uniqKey="Veit S" first="Svenja" last="Veit">Svenja Veit</name>
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</record>
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