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    A Novel DNA and Protein Combination COVID-19 Vaccine Formulation Provides Full Protection against SARS-CoV-2 in Rhesus Macaques

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    Authors
    Li, Yuzhong
    Hu, Guangnan
    Wang, Shixia
    Li, Qihan
    Lu, Shan
    Cun, Wei
    UMass Chan Affiliations
    Department of Medicine
    Document Type
    Accepted Manuscript
    Publication Date
    2021-02-08
    Keywords
    DNA vaccine
    COVID-19
    SARS-CoV-2
    non-human primate
    protein vaccine
    spike glycoprotein
    Amino Acids, Peptides, and Proteins
    Hemic and Immune Systems
    Immunology of Infectious Disease
    Immunoprophylaxis and Therapy
    Infectious Disease
    Virology
    Virus Diseases
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    Abstract
    The current study aims to develop a safe and highly immunogenic COVID-19 vaccine. The novel combination of a DNA vaccine encoding the full-length Spike (S) protein of SARS-CoV-2 and a recombinant S1 protein vaccine induced high level neutralizing antibody and T cell immune responses in both small and large animal models. More significantly, the co-delivery of DNA and protein components at the same time elicited full protection against intratracheal challenge of SARS-CoV-2 viruses in immunized rhesus macaques. As both DNA and protein vaccines have been proven safe in previous human studies, and DNA vaccines are capable of eliciting germinal center B cell development, which is critical for high -affinity memory B cell responses, the DNA and protein co-delivery vaccine approach has great potential to serve as a safe and effective approach to develop COVID-19 vaccines that provide long-term protection.
    Source

    Li Y, Bi Y, Xiao H, Yao Y, Liu X, Hu Z, Duan J, Yang Y, Li Z, Li Y, Zhang H, Ding C, Yang J, Li H, He Z, Liu L, Hu G, Liu S, Che Y, Wang S, Li Q, Lu S, Cun W. A Novel DNA and Protein Combination COVID-19 Vaccine Formulation Provides Full Protection against SARS-CoV-2 in Rhesus Macaques. Emerg Microbes Infect. 2021 Feb 8:1-19. doi: 10.1080/22221751.2021.1887767. Epub ahead of print. PMID: 33555988. Link to article on publisher's site

    DOI
    10.1080/22221751.2021.1887767
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/27384
    PubMed ID
    33555988
    Notes

    Full author list omitted for brevity. For the full list of authors, see article.

    Related Resources

    Link to Article in PubMed

    Rights
    This is an Accepted Manuscript version of the following article: Emerg Microbes Infect. 2021 Feb 8:1-19. doi: 10.1080/22221751.2021.1887767. Accepted manuscript posted as allowed by the publisher's green open access sharing policy at https://authorservices.taylorandfrancis.com/publishing-open-access/.
    ae974a485f413a2113503eed53cd6c53
    10.1080/22221751.2021.1887767
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