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Host Genetic Variation Impacts SARS-CoV-2 Vaccination Response in the Diversity Outbred Mouse Population.
Cruz Cisneros, Marta C; Anderson, Elizabeth J; Hampton, Brea K; Parotti, Breantié; Sarkar, Sanjay; Taft-Benz, Sharon; Bell, Timothy A; Blanchard, Matthew; Dillard, Jacob A; Dinnon, Kenneth H; Hock, Pablo; Leist, Sarah R; Madden, Emily A; Shaw, Ginger D; West, Ande; Baric, Ralph S; Baxter, Victoria K; Pardo-Manuel de Villena, Fernando; Heise, Mark T; Ferris, Martin T.
Afiliación
  • Cruz Cisneros MC; Genetics and Molecular Biology Curriculum, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Anderson EJ; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Hampton BK; Division of Comparative Medicine, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Parotti B; Genetics and Molecular Biology Curriculum, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Sarkar S; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Taft-Benz S; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Bell TA; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Blanchard M; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Dillard JA; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Dinnon KH; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Hock P; Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Leist SR; Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Madden EA; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Shaw GD; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
  • West A; Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Baric RS; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Baxter VK; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
  • Pardo-Manuel de Villena F; Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Heise MT; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
  • Ferris MT; Division of Comparative Medicine, University of North Carolina, Chapel Hill, NC 27599, USA.
Vaccines (Basel) ; 12(1)2024 Jan 20.
Article en En | MEDLINE | ID: mdl-38276675
ABSTRACT
The COVID-19 pandemic led to the rapid and worldwide development of highly effective vaccines against SARS-CoV-2. However, there is significant individual-to-individual variation in vaccine efficacy due to factors including viral variants, host age, immune status, environmental and host genetic factors. Understanding those determinants driving this variation may inform the development of more broadly protective vaccine strategies. While host genetic factors are known to impact vaccine efficacy for respiratory pathogens such as influenza and tuberculosis, the impact of host genetic variation on vaccine efficacy against COVID-19 is not well understood. To model the impact of host genetic variation on SARS-CoV-2 vaccine efficacy, while controlling for the impact of non-genetic factors, we used the Diversity Outbred (DO) mouse model. We found that DO mice immunized against SARS-CoV-2 exhibited high levels of variation in vaccine-induced neutralizing antibody responses. While the majority of the vaccinated mice were protected from virus-induced disease, similar to human populations, we observed vaccine breakthrough in a subset of mice. Importantly, we found that this variation in neutralizing antibody, virus-induced disease, and viral titer is heritable, indicating that the DO serves as a useful model system for studying the contribution of genetic variation of both vaccines and disease outcomes.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Vaccines (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Vaccines (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos