Serveur d'exploration MERS

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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 : 000A50

CD8+ 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 :

RBID : PMC:6316859

Descripteurs français

English descriptors

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:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<email>sylvia.jany@micro.vetmed.uni-muenchen.de</email>
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<term>Animals</term>
<term>Antibodies, Neutralizing (immunology)</term>
<term>Antibodies, Viral (immunology)</term>
<term>CD8-Positive T-Lymphocytes (immunology)</term>
<term>Coronavirus Infections (immunology)</term>
<term>Epitopes, T-Lymphocyte (immunology)</term>
<term>Female</term>
<term>Immunity, Cellular</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Middle East Respiratory Syndrome Coronavirus (immunology)</term>
<term>Nucleocapsid Proteins (genetics)</term>
<term>Nucleocapsid Proteins (immunology)</term>
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<term>Animaux</term>
<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>
<term>Infections à coronavirus (immunologie)</term>
<term>Lymphocytes T CD8+ (immunologie)</term>
<term>Protéines nucléocapside (génétique)</term>
<term>Protéines nucléocapside (immunologie)</term>
<term>Protéines recombinantes (immunologie)</term>
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<term>Souris de lignée BALB C</term>
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<term>Vaccins antiviraux (immunologie)</term>
<term>Virus de la vaccine (génétique)</term>
<term>Virus de la vaccine (immunologie)</term>
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<term>Nucleocapsid Proteins</term>
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<term>Antibodies, Neutralizing</term>
<term>Antibodies, Viral</term>
<term>Epitopes, T-Lymphocyte</term>
<term>Nucleocapsid Proteins</term>
<term>Recombinant Proteins</term>
<term>Viral Vaccines</term>
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<term>Vaccinia virus</term>
</keywords>
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<term>Protéines nucléocapside</term>
<term>Virus de la vaccine</term>
</keywords>
<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr">
<term>Anticorps antiviraux</term>
<term>Anticorps neutralisants</term>
<term>Coronavirus du syndrome respiratoire du Moyen-Orient</term>
<term>Déterminants antigéniques des lymphocytes T</term>
<term>Infections à coronavirus</term>
<term>Lymphocytes T CD8+</term>
<term>Protéines nucléocapside</term>
<term>Protéines recombinantes</term>
<term>Vaccins antiviraux</term>
<term>Virus de la vaccine</term>
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<term>CD8-Positive T-Lymphocytes</term>
<term>Coronavirus Infections</term>
<term>Middle East Respiratory Syndrome Coronavirus</term>
<term>Vaccinia virus</term>
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<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>
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<list>
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<li>Bavière</li>
<li>District de Haute-Bavière</li>
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<li>Munich</li>
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</record>

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