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Live-attenuated bivalent measles virus-derived vaccines targeting Middle East respiratory syndrome coronavirus induce robust and multifunctional T cell responses against both viruses in an appropriate mouse model

Identifieur interne : 000921 ( Main/Exploration ); précédent : 000920; suivant : 000922

Live-attenuated bivalent measles virus-derived vaccines targeting Middle East respiratory syndrome coronavirus induce robust and multifunctional T cell responses against both viruses in an appropriate mouse model

Auteurs : Bianca S. Bodmer [Allemagne] ; Anna H. Fiedler [Allemagne] ; Jan R. H. Hanauer [Allemagne] ; Steffen Prüfer [Allemagne] ; Michael D. Mühlebach [Allemagne]

Source :

RBID : PMC:7118890

Descripteurs français

English descriptors

Abstract

Cases of Middle East respiratory syndrome coronavirus (MERS-CoV) continue to occur, making it one of the WHO´s targets for accelerated vaccine development. One vaccine candidate is based on live-attenuated measles virus (MV) vaccine encoding the MERS-CoV spike glycoprotein (MERS-S). MVvac2-MERS-S(H) induces robust humoral and cellular immunity against MERS-S mediating protection. Here, the induction and nature of immunity after vaccination with MVvac2-MERS-S(H) or novel MVvac2-MERS-N were further characterized. We focused on the necessity for vector replication and the nature of induced T cells, since functional CD8+ T cells contribute importantly to clearance of MERS-CoV. While no immunity against MERS-CoV or MV was detected in MV-susceptible mice after immunization with UV-inactivated virus, replication-competent MVvac2-MERS-S(H) triggered robust neutralizing antibody titers also in adult mice. Furthermore, a significant fraction of MERS CoV-specific CD8+ T cells and MV-specific CD4+ T cells simultaneously expressing IFN-γ and TNF-α were induced, revealing that MVvac2-MERS-S(H) induces multifunctional cellular immunity.


Url:
DOI: 10.1016/j.virol.2018.05.028
PubMed: 29902727
PubMed Central: 7118890


Affiliations:


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Le document en format XML

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<term>Animals</term>
<term>Antibodies, Neutralizing (blood)</term>
<term>Antibodies, Viral (blood)</term>
<term>CD8-Positive T-Lymphocytes (immunology)</term>
<term>Coronavirus Infections (immunology)</term>
<term>Coronavirus Infections (prevention & control)</term>
<term>Disease Models, Animal</term>
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<term>Middle East Respiratory Syndrome Coronavirus (immunology)</term>
<term>Spike Glycoprotein, Coronavirus (genetics)</term>
<term>Spike Glycoprotein, Coronavirus (immunology)</term>
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<term>Glycoprotéine de spicule des coronavirus (génétique)</term>
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<term>Infections à coronavirus (immunologie)</term>
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<term>Modèles animaux de maladie humaine</term>
<term>Souris de lignée BALB C</term>
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<term>Vaccins antiviraux (immunologie)</term>
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<term>Viral Vaccines</term>
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<term>Glycoprotéine de spicule des coronavirus</term>
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<term>Viral Vaccines</term>
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<term>Anticorps neutralisants</term>
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<p>Cases of Middle East respiratory syndrome coronavirus (MERS-CoV) continue to occur, making it one of the WHO´s targets for accelerated vaccine development. One vaccine candidate is based on live-attenuated measles virus (MV) vaccine encoding the MERS-CoV spike glycoprotein (MERS-S). MV
<sub>vac2</sub>
-MERS-S(H) induces robust humoral and cellular immunity against MERS-S mediating protection. Here, the induction and nature of immunity after vaccination with MV
<sub>vac2</sub>
-MERS-S(H) or novel MV
<sub>vac2</sub>
-MERS-N were further characterized. We focused on the necessity for vector replication and the nature of induced T cells, since functional CD8
<sup>+</sup>
T cells contribute importantly to clearance of MERS-CoV. While no immunity against MERS-CoV or MV was detected in MV-susceptible mice after immunization with UV-inactivated virus, replication-competent MV
<sub>vac2</sub>
-MERS-S(H) triggered robust neutralizing antibody titers also in adult mice. Furthermore, a significant fraction of MERS CoV-specific CD8
<sup>+</sup>
T cells and MV-specific CD4
<sup>+</sup>
T cells simultaneously expressing IFN-γ and TNF-α were induced, revealing that MV
<sub>vac2</sub>
-MERS-S(H) induces multifunctional cellular immunity.</p>
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<li>Allemagne</li>
</country>
</list>
<tree>
<country name="Allemagne">
<noRegion>
<name sortKey="Bodmer, Bianca S" sort="Bodmer, Bianca S" uniqKey="Bodmer B" first="Bianca S." last="Bodmer">Bianca S. Bodmer</name>
</noRegion>
<name sortKey="Bodmer, Bianca S" sort="Bodmer, Bianca S" uniqKey="Bodmer B" first="Bianca S." last="Bodmer">Bianca S. Bodmer</name>
<name sortKey="Fiedler, Anna H" sort="Fiedler, Anna H" uniqKey="Fiedler A" first="Anna H." last="Fiedler">Anna H. Fiedler</name>
<name sortKey="Fiedler, Anna H" sort="Fiedler, Anna H" uniqKey="Fiedler A" first="Anna H." last="Fiedler">Anna H. Fiedler</name>
<name sortKey="Hanauer, Jan R H" sort="Hanauer, Jan R H" uniqKey="Hanauer J" first="Jan R. H." last="Hanauer">Jan R. H. Hanauer</name>
<name sortKey="Muhlebach, Michael D" sort="Muhlebach, Michael D" uniqKey="Muhlebach M" first="Michael D." last="Mühlebach">Michael D. Mühlebach</name>
<name sortKey="Muhlebach, Michael D" sort="Muhlebach, Michael D" uniqKey="Muhlebach M" first="Michael D." last="Mühlebach">Michael D. Mühlebach</name>
<name sortKey="Prufer, Steffen" sort="Prufer, Steffen" uniqKey="Prufer S" first="Steffen" last="Prüfer">Steffen Prüfer</name>
</country>
</tree>
</affiliations>
</record>

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