Article: SARS vaccine based on a replication-defective recombinant vesicular stomatitis virus is more potent than one based on a replication-competent vector.
2008 Volume 376, Issue 1, Page(s) 165–172
Abstract: ... U., Rose, J. K., Lamirande, E., Vogel, L., Subbarao, K., Roberts, A., 2005. Long-term protection ... the SARS-CoV S protein provides long-term protection of immunized mice from SARS-CoV infection (Kapadia, S ...
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. |
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MeSH term(s) | 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 |
Chemical Substances | Antibodies, Viral ; G protein, vesicular stomatitis virus ; Membrane Glycoproteins ; Spike Glycoprotein, Coronavirus ; Viral Envelope Proteins ; Viral Vaccines ; spike glycoprotein, SARS-CoV ; spike protein, mouse hepatitis virus |
Keywords | covid19 |
Language | English |
Publishing date | 2008-04-08 |
Publishing country | United States |
Document type | Journal Article ; Research Support, N.I.H., Extramural |
ZDB-ID | 200425-2 |
ISSN | 1096-0341 ; 0042-6822 |
ISSN (online) | 1096-0341 |
ISSN | 0042-6822 |
DOI | 10.1016/j.virol.2008.03.002 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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