Host Genetic Variation Impacts SARS-CoV-2 Vaccination Response in the Diversity Outbred Mouse Population

Author:

Cruz Cisneros Marta C.12ORCID,Anderson Elizabeth J.3ORCID,Hampton Brea K.12ORCID,Parotti Breantié2,Sarkar Sanjay2,Taft-Benz Sharon2,Bell Timothy A.2ORCID,Blanchard Matthew2,Dillard Jacob A.4ORCID,Dinnon Kenneth H.4,Hock Pablo2,Leist Sarah R.5ORCID,Madden Emily A.4ORCID,Shaw Ginger D.2ORCID,West Ande5,Baric Ralph S.45ORCID,Baxter Victoria K.367ORCID,Pardo-Manuel de Villena Fernando28,Heise Mark T.248,Ferris Martin T.2ORCID

Affiliation:

1. Genetics and Molecular Biology Curriculum, University of North Carolina, Chapel Hill, NC 27599, USA

2. Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA

3. Division of Comparative Medicine, University of North Carolina, Chapel Hill, NC 27599, USA

4. Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC 27599, USA

5. Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

6. Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, NC 27599, USA

7. Texas Biomedical Research Institute, San Antonio, TX 78227, USA

8. Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC 27599, USA

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.

Funder

NIH

Burroughs Wellcome Fund

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

Reference79 articles.

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