SARS vaccine based on a replication-defective recombinant vesicular stomatitis virus is more potent than one based on a replication-competent vector.
Identifieur interne : 001B73 ( PubMed/Curation ); précédent : 001B72; suivant : 001B74SARS vaccine based on a replication-defective recombinant vesicular stomatitis virus is more potent than one based on a replication-competent vector.
Auteurs : Sagar U. Kapadia [États-Unis] ; Ian D. Simon ; John K. RoseSource :
- Virology [ 0042-6822 ] ; 2008.
Descripteurs français
- KwdFr :
- Animaux, Anticorps antiviraux (sang), Glycoprotéine de spicule des coronavirus, Glycoprotéines membranaires (génétique), Glycoprotéines membranaires (immunologie), Injections musculaires, Protéines de l'enveloppe virale (génétique), Protéines de l'enveloppe virale (immunologie), Réplication virale (génétique), Réplication virale (immunologie), Souris, Souris de lignée BALB C, Tests de neutralisation, Vaccins antiviraux (génétique), Vaccins antiviraux (immunologie), Vecteurs génétiques, Virus de la stomatite vésiculeuse de type Indiana (génétique), Virus du SRAS (génétique), Virus du SRAS (immunologie).
- MESH :
- génétique : Glycoprotéines membranaires, Protéines de l'enveloppe virale, Réplication virale, Vaccins antiviraux, Virus de la stomatite vésiculeuse de type Indiana, Virus du SRAS.
- immunologie : Glycoprotéines membranaires, Protéines de l'enveloppe virale, Réplication virale, Vaccins antiviraux, Virus du SRAS.
- sang : Anticorps antiviraux.
- Animaux, Glycoprotéine de spicule des coronavirus, Injections musculaires, Souris, Souris de lignée BALB C, Tests de neutralisation, Vecteurs génétiques.
English descriptors
- KwdEn :
- Animals, Antibodies, Viral (blood), Genetic Vectors, Injections, Intramuscular, Membrane Glycoproteins (genetics), Membrane Glycoproteins (immunology), Mice, Mice, Inbred BALB C, Neutralization Tests, SARS Virus (genetics), SARS Virus (immunology), Spike Glycoprotein, Coronavirus, Vesicular stomatitis Indiana virus (genetics), Viral Envelope Proteins (genetics), Viral Envelope Proteins (immunology), Viral Vaccines (genetics), Viral Vaccines (immunology), Virus Replication (genetics), Virus Replication (immunology).
- MESH :
- chemical , blood : Antibodies, Viral.
- chemical , genetics : Membrane Glycoproteins, Viral Envelope Proteins, Viral Vaccines.
- chemical , immunology : Membrane Glycoproteins, Viral Envelope Proteins, Viral Vaccines.
- genetics : SARS Virus, Vesicular stomatitis Indiana virus, Virus Replication.
- immunology : SARS Virus, Virus Replication.
- Animals, Genetic Vectors, Injections, Intramuscular, Mice, Mice, Inbred BALB C, Neutralization Tests, Spike Glycoprotein, Coronavirus.
Abstract
A SARS vaccine based on a live-attenuated vesicular stomatitis virus (VSV) recombinant expressing the SARS-CoV S protein provides long-term protection of immunized mice from SARS-CoV infection (Kapadia, S.U., Rose, J. K., Lamirande, E., Vogel, L., Subbarao, K., Roberts, A., 2005. Long-term protection from SARS coronavirus infection conferred by a single immunization with an attenuated VSV-based vaccine. Virology 340(2), 174-82.). Because it is difficult to obtain regulatory approval of vaccine based on live viruses, we constructed a replication-defective single-cycle VSV vector in which we replaced the VSV glycoprotein (G) gene with the SARS-CoV S gene. The virus was only able to infect cells when pseudotyped with the VSV G protein. We measured the effectiveness of immunization with the single-cycle vaccine in mice. We found that the vaccine given intramuscularly induced a neutralizing antibody response to SARS-CoV that was approximately ten-fold greater than that required for the protection from SARS-CoV infection, and significantly greater than that generated by the replication-competent vector expressing SARS-CoV S protein given by the same route. Our results, along with earlier studies showing potent induction of T-cell responses by single-cycle vectors, indicate that these vectors are excellent alternatives to live-attenuated VSV.
DOI: 10.1016/j.virol.2008.03.002
PubMed: 18396306
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pubmed:18396306Le document en format XML
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<front><div type="abstract" xml:lang="en">A SARS vaccine based on a live-attenuated vesicular stomatitis virus (VSV) recombinant expressing the SARS-CoV S protein provides long-term protection of immunized mice from SARS-CoV infection (Kapadia, S.U., Rose, J. K., Lamirande, E., Vogel, L., Subbarao, K., Roberts, A., 2005. Long-term protection from SARS coronavirus infection conferred by a single immunization with an attenuated VSV-based vaccine. Virology 340(2), 174-82.). Because it is difficult to obtain regulatory approval of vaccine based on live viruses, we constructed a replication-defective single-cycle VSV vector in which we replaced the VSV glycoprotein (G) gene with the SARS-CoV S gene. The virus was only able to infect cells when pseudotyped with the VSV G protein. We measured the effectiveness of immunization with the single-cycle vaccine in mice. We found that the vaccine given intramuscularly induced a neutralizing antibody response to SARS-CoV that was approximately ten-fold greater than that required for the protection from SARS-CoV infection, and significantly greater than that generated by the replication-competent vector expressing SARS-CoV S protein given by the same route. Our results, along with earlier studies showing potent induction of T-cell responses by single-cycle vectors, indicate that these vectors are excellent alternatives to live-attenuated VSV.</div>
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