A prime-boost vaccination protocol optimizes immune responses against the nucleocapsid protein of the SARS coronavirus
Identifieur interne : 003521 ( Main/Exploration ); précédent : 003520; suivant : 003522A prime-boost vaccination protocol optimizes immune responses against the nucleocapsid protein of the SARS coronavirus
Auteurs : Kai Schulze [Allemagne] ; Caroline Staib [Allemagne] ; Hermann M. Sch Tzl [Allemagne] ; Thomas Ebensen [Allemagne] ; Volker Erfle [Allemagne] ; Carlos A. Guzman [Allemagne]Source :
- Vaccine [ 0264-410X ] ; 2008.
Descripteurs français
- KwdFr :
- Adjuvants immunologiques, Administration par voie nasale, Animaux, Anticorps antiviraux (immunologie), Immunité cellulaire, Immunoglobuline A (immunologie), Injections musculaires, Lipopeptides (immunologie), Protéines nucléocapside (immunologie), Rappel de vaccin (), Souris, Souris de lignée BALB C, Syndrome respiratoire aigu sévère (), Syndrome respiratoire aigu sévère (immunologie), Vaccins antiviraux (administration et posologie), Vaccins antiviraux (immunologie), Virus de la vaccine (immunologie), Virus du SRAS (immunologie).
- MESH :
- administration et posologie : Vaccins antiviraux.
- immunologie : Anticorps antiviraux, Immunoglobuline A, Lipopeptides, Protéines nucléocapside, Syndrome respiratoire aigu sévère, Vaccins antiviraux, Virus de la vaccine, Virus du SRAS.
- Pascal (Inist)
- Adjuvants immunologiques, Administration par voie nasale, Animaux, Immunité cellulaire, Injections musculaires, Rappel de vaccin, Souris, Souris de lignée BALB C, Syndrome respiratoire aigu sévère, Virus syndrome respiratoire aigu sévère, Virus vaccine, Vaccination, Réponse immune, Nucléocapside, Protéine, Adjuvant immunologique, Muqueuse, Immunisation, Vaccin.
- Wicri :
- topic : Vaccination, Vaccin.
English descriptors
- KwdEn :
- Adjuvants, Immunologic, Administration, Intranasal, Animals, Antibodies, Viral (immunology), Immune response, Immunity, Cellular, Immunization, Immunization, Secondary (methods), Immunoglobulin A (immunology), Immunological adjuvant, Injections, Intramuscular, Lipopeptides (immunology), Mice, Mice, Inbred BALB C, Mucosa, Nucleocapsid, Nucleocapsid Proteins (immunology), Protein, SARS Virus (immunology), Severe Acute Respiratory Syndrome (immunology), Severe Acute Respiratory Syndrome (prevention & control), Severe acute respiratory syndrome virus, Vaccination, Vaccine, Vaccinia virus, Vaccinia virus (immunology), Viral Vaccines (administration & dosage), Viral Vaccines (immunology).
- MESH :
- chemical , administration & dosage : Viral Vaccines.
- chemical , immunology : Antibodies, Viral, Immunoglobulin A, Lipopeptides, Nucleocapsid Proteins, Viral Vaccines.
- chemical : Adjuvants, Immunologic.
- immunology : SARS Virus, Severe Acute Respiratory Syndrome, Vaccinia virus.
- methods : Immunization, Secondary.
- prevention & control : Severe Acute Respiratory Syndrome.
- Administration, Intranasal, Animals, Immunity, Cellular, Injections, Intramuscular, Mice, Mice, Inbred BALB C.
Abstract
Severe acute respiratory syndrome (SARS) is a serious infectious disease caused by the SARS coronavirus. We assessed the potential of prime-boost vaccination protocols based on the nucleocapsid (NC) protein co-administered with a derivative of the mucosal adjuvant MALP-2 or expressed by modified Vaccinia virus Ankara (MVA-NC) to stimulate humoral and cellular immune responses at systemic and mucosal levels. The obtained results demonstrated that strong immune responses can be elicited both at systemic and mucosal levels following a heterologous prime-boost vaccination protocol consisting in priming with NC protein add-mixed with MALP-2 by intranasal route and boosting with MVA-NC by intramuscular route.
Url:
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) is a serious infectious disease caused by the SARS coronavirus. We assessed the potential of prime-boost vaccination protocols based on the nucleocapsid (NC) protein co-administered with a derivative of the mucosal adjuvant MALP-2 or expressed by modified Vaccinia virus Ankara (MVA-NC) to stimulate humoral and cellular immune responses at systemic and mucosal levels. The obtained results demonstrated that strong immune responses can be elicited both at systemic and mucosal levels following a heterologous prime-boost vaccination protocol consisting in priming with NC protein add-mixed with MALP-2 by intranasal route and boosting with MVA-NC by intramuscular route.</div>
</front>
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<name sortKey="Ebensen, Thomas" sort="Ebensen, Thomas" uniqKey="Ebensen T" first="Thomas" last="Ebensen">Thomas Ebensen</name>
<name sortKey="Erfle, Volker" sort="Erfle, Volker" uniqKey="Erfle V" first="Volker" last="Erfle">Volker Erfle</name>
<name sortKey="Erfle, Volker" sort="Erfle, Volker" uniqKey="Erfle V" first="Volker" last="Erfle">Volker Erfle</name>
<name sortKey="Guzman, Carlos A" sort="Guzman, Carlos A" uniqKey="Guzman C" first="Carlos A." last="Guzman">Carlos A. Guzman</name>
<name sortKey="Sch Tzl, Hermann M" sort="Sch Tzl, Hermann M" uniqKey="Sch Tzl H" first="Hermann M." last="Sch Tzl">Hermann M. Sch Tzl</name>
<name sortKey="Staib, Caroline" sort="Staib, Caroline" uniqKey="Staib C" first="Caroline" last="Staib">Caroline Staib</name>
<name sortKey="Staib, Caroline" sort="Staib, Caroline" uniqKey="Staib C" first="Caroline" last="Staib">Caroline Staib</name>
</country>
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