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Novel virus-like nanoparticle vaccine effectively protects animal model from SARS-CoV-2 infection.
Geng, Qibin; Tai, Wanbo; Baxter, Victoria K; Shi, Juan; Wan, Yushun; Zhang, Xiujuan; Montgomery, Stephanie A; Taft-Benz, Sharon A; Anderson, Elizabeth J; Knight, Audrey C; Dinnon, Kenneth H; Leist, Sarah R; Baric, Ralph S; Shang, Jian; Hong, Sung-Wook; Drelich, Aleksandra; Tseng, Chien-Te K; Jenkins, Marc; Heise, Mark; Du, Lanying; Li, Fang.
  • Geng Q; Department of Veterinary and Biomedical Sciences, University of Minnesota, Saint Paul, Minnesota, United States of America.
  • Tai W; Center for Coronavirus Research, University of Minnesota, Saint Paul, Minnesota, United States of America.
  • Baxter VK; Laboratory of Viral Immunology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, New York, United States of America.
  • Shi J; Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Wan Y; Division of Comparative Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Zhang X; Laboratory of Viral Immunology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, New York, United States of America.
  • Montgomery SA; Department of Veterinary and Biomedical Sciences, University of Minnesota, Saint Paul, Minnesota, United States of America.
  • Taft-Benz SA; Center for Coronavirus Research, University of Minnesota, Saint Paul, Minnesota, United States of America.
  • Anderson EJ; Laboratory of Viral Immunology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, New York, United States of America.
  • Knight AC; Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Dinnon KH; Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Leist SR; Division of Comparative Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Baric RS; Division of Comparative Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Shang J; Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Hong SW; Rapidly Emerging Antiviral Drug Development Initiative, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Drelich A; Division of Comparative Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Tseng CK; Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Jenkins M; Rapidly Emerging Antiviral Drug Development Initiative, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Heise M; Department of Veterinary and Biomedical Sciences, University of Minnesota, Saint Paul, Minnesota, United States of America.
  • Du L; Center for Coronavirus Research, University of Minnesota, Saint Paul, Minnesota, United States of America.
  • Li F; Center for Immunology, Department of Microbiology and Immunology, University of Minnesota, Minneapolis, Minnesota, United States of America.
PLoS Pathog ; 17(9): e1009897, 2021 09.
Article in English | MEDLINE | ID: covidwho-1398941
ABSTRACT
The key to battling the COVID-19 pandemic and its potential aftermath is to develop a variety of vaccines that are efficacious and safe, elicit lasting immunity, and cover a range of SARS-CoV-2 variants. Recombinant viral receptor-binding domains (RBDs) are safe vaccine candidates but often have limited efficacy due to the lack of virus-like immunogen display pattern. Here we have developed a novel virus-like nanoparticle (VLP) vaccine that displays 120 copies of SARS-CoV-2 RBD on its surface. This VLP-RBD vaccine mimics virus-based vaccines in immunogen display, which boosts its efficacy, while maintaining the safety of protein-based subunit vaccines. Compared to the RBD vaccine, the VLP-RBD vaccine induced five times more neutralizing antibodies in mice that efficiently blocked SARS-CoV-2 from attaching to its host receptor and potently neutralized the cell entry of variant SARS-CoV-2 strains, SARS-CoV-1, and SARS-CoV-1-related bat coronavirus. These neutralizing immune responses induced by the VLP-RBD vaccine did not wane during the two-month study period. Furthermore, the VLP-RBD vaccine effectively protected mice from SARS-CoV-2 challenge, dramatically reducing the development of clinical signs and pathological changes in immunized mice. The VLP-RBD vaccine provides one potentially effective solution to controlling the spread of SARS-CoV-2.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: Nanoparticles / Immunogenicity, Vaccine / COVID-19 Vaccines / COVID-19 Type of study: Experimental Studies / Prognostic study Topics: Vaccines / Variants Limits: Animals / Female / Humans Language: English Journal: PLoS Pathog Year: 2021 Document Type: Article Affiliation country: Journal.ppat.1009897

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Nanoparticles / Immunogenicity, Vaccine / COVID-19 Vaccines / COVID-19 Type of study: Experimental Studies / Prognostic study Topics: Vaccines / Variants Limits: Animals / Female / Humans Language: English Journal: PLoS Pathog Year: 2021 Document Type: Article Affiliation country: Journal.ppat.1009897