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  1. Article: SARS vaccine based on a replication-defective recombinant vesicular stomatitis virus is more potent than one based on a replication-competent vector.

    Kapadia, Sagar U / Simon, Ian D / Rose, John K

    Virology

    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.
    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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  2. Article: Long-term protection from SARS coronavirus infection conferred by a single immunization with an attenuated VSV-based vaccine.

    Kapadia, Sagar U / Rose, John K / Lamirande, Elaine / Vogel, Leatrice / Subbarao, Kanta / Roberts, Anjeanette

    Virology

    2005  Volume 340, Issue 2, Page(s) 174–182

    Abstract: Although the recent SARS coronavirus (SARS-CoV) that appeared in 2002 has now been contained, the possibility of re-emergence of SARS-CoV remains. Due to the threat of re-emergence, the overall fatality rate of approximately 10%, and the rapid dispersion ...

    Abstract Although the recent SARS coronavirus (SARS-CoV) that appeared in 2002 has now been contained, the possibility of re-emergence of SARS-CoV remains. Due to the threat of re-emergence, the overall fatality rate of approximately 10%, and the rapid dispersion of the virus via international travel, viable vaccine candidates providing protection from SARS are clearly needed. We developed an attenuated VSV recombinant (VSV-S) expressing the SARS coronavirus (SARS-CoV) spike (S) protein. In cells infected with this recombinant, S protein was synthesized, glycosylated at approximately 17 Asn residues, and transported via the Golgi to the cell surface. Mice vaccinated with VSV-S developed SARS-neutralizing antibody and were able to control a challenge with SARS-CoV performed at 1 month or 4 months after a single vaccination. We also demonstrated, by passive antibody transfer, that the antibody response induced by the vaccine was sufficient for controlling SARS-CoV infection. A VSV-vectored SARS vaccine could have significant advantages over other SARS vaccine candidates described to date.
    MeSH term(s) Animals ; Antibody Formation ; Cell Line ; Cricetinae ; DNA Primers ; Immunity, Cellular ; Kidney ; Mice ; Reverse Transcriptase Polymerase Chain Reaction ; SARS Virus/genetics ; SARS Virus/immunology ; Severe Acute Respiratory Syndrome/immunology ; Vaccines, Attenuated ; Vaccines, DNA ; Vesicular stomatitis Indiana virus/immunology ; Viral Vaccines
    Chemical Substances DNA Primers ; Vaccines, Attenuated ; Vaccines, DNA ; Viral Vaccines
    Keywords covid19
    Language English
    Publishing date 2005-07-19
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 200425-2
    ISSN 1096-0341 ; 0042-6822
    ISSN (online) 1096-0341
    ISSN 0042-6822
    DOI 10.1016/j.virol.2005.06.016
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Comparative Outcomes of Transcatheter Aortic Valve Implantation and Mitral Transcatheter Edge-to-Edge Repair: Same Versus Different Hospitalization.

    Sagheer, Shazib / Minhas, Abdul Mannan Khan / Arshad, Hassaan Bin / Nazir, Salik / Ijaz, Sardar Hassan / Ullah, Waqas / Khan, Safi U / Kleiman, Neal S / Kapadia, Samir R / Goel, Sachin S

    The American journal of cardiology

    2021  Volume 164, Page(s) 133–135

    MeSH term(s) Acute Kidney Injury/epidemiology ; Aged ; Aged, 80 and over ; Aortic Valve Stenosis/complications ; Aortic Valve Stenosis/physiopathology ; Aortic Valve Stenosis/surgery ; Assisted Circulation/statistics & numerical data ; Cardiac Catheterization/methods ; Disease Progression ; Female ; Hospital Mortality ; Hospitalization ; Humans ; Length of Stay ; Male ; Mitral Valve Annuloplasty/methods ; Mitral Valve Insufficiency/complications ; Mitral Valve Insufficiency/physiopathology ; Mitral Valve Insufficiency/surgery ; Postoperative Complications/epidemiology ; Postoperative Complications/therapy ; Respiration, Artificial/statistics & numerical data ; Shock, Cardiogenic/epidemiology ; Stroke Volume ; Transcatheter Aortic Valve Replacement/methods
    Language English
    Publishing date 2021-11-08
    Publishing country United States
    Document type Comparative Study ; Letter
    ZDB-ID 80014-4
    ISSN 1879-1913 ; 0002-9149
    ISSN (online) 1879-1913
    ISSN 0002-9149
    DOI 10.1016/j.amjcard.2021.10.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Utility of the aged BALB/c mouse model to demonstrate prevention and control strategies for severe acute respiratory syndrome coronavirus (SARS-CoV).

    Vogel, Leatrice N / Roberts, Anjeanette / Paddock, Christopher D / Genrich, Gillian L / Lamirande, Elaine W / Kapadia, Sagar U / Rose, John K / Zaki, Sherif R / Subbarao, Kanta

    Vaccine

    2006  Volume 25, Issue 12, Page(s) 2173–2179

    Abstract: The causative agent of Severe Acute Respiratory Syndrome (SARS) was identified as a coronavirus (CoV) following the outbreak of 2002-2003. There are currently no licensed vaccines or treatments for SARS-CoV infections. Potential prevention and control ... ...

    Abstract The causative agent of Severe Acute Respiratory Syndrome (SARS) was identified as a coronavirus (CoV) following the outbreak of 2002-2003. There are currently no licensed vaccines or treatments for SARS-CoV infections. Potential prevention and control strategies that show promise in vitro must be evaluated in animal models. The aged BALB/c mouse model for SARS supports a high level of viral replication in association with clinical illness and disease that mimics SARS in the elderly. We tested two preventive strategies, vaccination and passive transfer of serum antibody, to determine the extent of protection achieved against SARS-CoV challenge in this model. These approaches were able to achieve or induce antibody titers sufficient to reduce viral load, protect from weight loss and reduce or eliminate histopathologic changes in the lungs of aged mice. This study validates the utility of the aged BALB/c mouse model for evaluation of the efficacy of vaccines and immunoprophylaxis.
    MeSH term(s) Animals ; Antibiotic Prophylaxis/methods ; Antibodies, Viral/immunology ; Immunization/methods ; Mice ; Mice, Inbred BALB C ; Models, Animal ; SARS Virus/immunology ; Severe Acute Respiratory Syndrome/immunology ; Severe Acute Respiratory Syndrome/prevention & control ; Severe Acute Respiratory Syndrome/virology ; Treatment Outcome ; Vaccination/methods ; Viral Vaccines/immunology
    Chemical Substances Antibodies, Viral ; Viral Vaccines
    Keywords covid19
    Language English
    Publishing date 2006-12-11
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, N.I.H., Intramural
    ZDB-ID 605674-x
    ISSN 1873-2518 ; 0264-410X
    ISSN (online) 1873-2518
    ISSN 0264-410X
    DOI 10.1016/j.vaccine.2006.11.055
    Database MEDical Literature Analysis and Retrieval System OnLINE

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