SARS-CoV-2 mRNA vaccines confer protection in diet-induced obese mice despite altered immune cell profiles in the lung

Abstract Hypertension, diabetes, and obesity are comorbidities that influence severe cases of COVID-19 and are associated with weak humoral immunity after vaccination. We hypothesized that the diet-induced obese (DIO) K18-hACE2 mouse model could be utilized to reveal sex and DIO- specific difference...

Full description

Saved in:
Bibliographic Details
Main Authors: Katherine S. Lee, Dylan T. Boehm, Olivia A. Miller-Stump, Nathaniel A. Rader, Melissa Cooper, Holly A. Cyphert, Emel Sen-Kilic, Mariette Barbier, F. Heath Damron
Format: Article
Language:English
Published: Nature Portfolio 2025-07-01
Series:Scientific Reports
Subjects:
Online Access:https://doi.org/10.1038/s41598-025-12320-z
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849333032061763584
author Katherine S. Lee
Dylan T. Boehm
Olivia A. Miller-Stump
Nathaniel A. Rader
Melissa Cooper
Holly A. Cyphert
Emel Sen-Kilic
Mariette Barbier
F. Heath Damron
author_facet Katherine S. Lee
Dylan T. Boehm
Olivia A. Miller-Stump
Nathaniel A. Rader
Melissa Cooper
Holly A. Cyphert
Emel Sen-Kilic
Mariette Barbier
F. Heath Damron
author_sort Katherine S. Lee
collection DOAJ
description Abstract Hypertension, diabetes, and obesity are comorbidities that influence severe cases of COVID-19 and are associated with weak humoral immunity after vaccination. We hypothesized that the diet-induced obese (DIO) K18-hACE2 mouse model could be utilized to reveal sex and DIO- specific differences in responses to COVID-19 immunization. To test this hypothesis, we immunized male and female DIO mice with a COVID-19 mRNA vaccine. Female DIO mice after immunization showed higher neutralizing antibody levels that recognized both SARS-CoV-2 variant RBD than male DIO mice. After Omicron SARS-CoV-2 challenge, single cell RNA sequencing analysis of lung tissue suggested decreased naïve B cell populations in immunized DIO mice in addition to an increase in macrophages in vaccinated female DIO mice. Analysis of viral burden revealed that the DIO variable did not impact immunity in immunized mice. Overall, this study underscores the ability of COVID-19 mRNA vaccines to confer protection in the comorbid SARS-CoV-2 murine challenge model.
format Article
id doaj-art-f0e40b82885d4e038babfbb12a2d52d0
institution Kabale University
issn 2045-2322
language English
publishDate 2025-07-01
publisher Nature Portfolio
record_format Article
series Scientific Reports
spelling doaj-art-f0e40b82885d4e038babfbb12a2d52d02025-08-20T03:46:00ZengNature PortfolioScientific Reports2045-23222025-07-0115111310.1038/s41598-025-12320-zSARS-CoV-2 mRNA vaccines confer protection in diet-induced obese mice despite altered immune cell profiles in the lungKatherine S. Lee0Dylan T. Boehm1Olivia A. Miller-Stump2Nathaniel A. Rader3Melissa Cooper4Holly A. Cyphert5Emel Sen-Kilic6Mariette Barbier7F. Heath Damron8Department of Microbiology, Immunology, and Cell Biology, West Virginia UniversityDepartment of Microbiology, Immunology, and Cell Biology, West Virginia UniversityDepartment of Microbiology, Immunology, and Cell Biology, West Virginia UniversityDepartment of Microbiology, Immunology, and Cell Biology, West Virginia UniversityDepartment of Microbiology, Immunology, and Cell Biology, West Virginia UniversityDepartment of Biological Sciences, Marshall UniversityDepartment of Microbiology, Immunology, and Cell Biology, West Virginia UniversityDepartment of Microbiology, Immunology, and Cell Biology, West Virginia UniversityDepartment of Microbiology, Immunology, and Cell Biology, West Virginia UniversityAbstract Hypertension, diabetes, and obesity are comorbidities that influence severe cases of COVID-19 and are associated with weak humoral immunity after vaccination. We hypothesized that the diet-induced obese (DIO) K18-hACE2 mouse model could be utilized to reveal sex and DIO- specific differences in responses to COVID-19 immunization. To test this hypothesis, we immunized male and female DIO mice with a COVID-19 mRNA vaccine. Female DIO mice after immunization showed higher neutralizing antibody levels that recognized both SARS-CoV-2 variant RBD than male DIO mice. After Omicron SARS-CoV-2 challenge, single cell RNA sequencing analysis of lung tissue suggested decreased naïve B cell populations in immunized DIO mice in addition to an increase in macrophages in vaccinated female DIO mice. Analysis of viral burden revealed that the DIO variable did not impact immunity in immunized mice. Overall, this study underscores the ability of COVID-19 mRNA vaccines to confer protection in the comorbid SARS-CoV-2 murine challenge model.https://doi.org/10.1038/s41598-025-12320-zSARS-CoV-2COVID-19DiabetesObesityK18-hACE2 transgenic mouseOmicron variant
spellingShingle Katherine S. Lee
Dylan T. Boehm
Olivia A. Miller-Stump
Nathaniel A. Rader
Melissa Cooper
Holly A. Cyphert
Emel Sen-Kilic
Mariette Barbier
F. Heath Damron
SARS-CoV-2 mRNA vaccines confer protection in diet-induced obese mice despite altered immune cell profiles in the lung
Scientific Reports
SARS-CoV-2
COVID-19
Diabetes
Obesity
K18-hACE2 transgenic mouse
Omicron variant
title SARS-CoV-2 mRNA vaccines confer protection in diet-induced obese mice despite altered immune cell profiles in the lung
title_full SARS-CoV-2 mRNA vaccines confer protection in diet-induced obese mice despite altered immune cell profiles in the lung
title_fullStr SARS-CoV-2 mRNA vaccines confer protection in diet-induced obese mice despite altered immune cell profiles in the lung
title_full_unstemmed SARS-CoV-2 mRNA vaccines confer protection in diet-induced obese mice despite altered immune cell profiles in the lung
title_short SARS-CoV-2 mRNA vaccines confer protection in diet-induced obese mice despite altered immune cell profiles in the lung
title_sort sars cov 2 mrna vaccines confer protection in diet induced obese mice despite altered immune cell profiles in the lung
topic SARS-CoV-2
COVID-19
Diabetes
Obesity
K18-hACE2 transgenic mouse
Omicron variant
url https://doi.org/10.1038/s41598-025-12320-z
work_keys_str_mv AT katherineslee sarscov2mrnavaccinesconferprotectionindietinducedobesemicedespitealteredimmunecellprofilesinthelung
AT dylantboehm sarscov2mrnavaccinesconferprotectionindietinducedobesemicedespitealteredimmunecellprofilesinthelung
AT oliviaamillerstump sarscov2mrnavaccinesconferprotectionindietinducedobesemicedespitealteredimmunecellprofilesinthelung
AT nathanielarader sarscov2mrnavaccinesconferprotectionindietinducedobesemicedespitealteredimmunecellprofilesinthelung
AT melissacooper sarscov2mrnavaccinesconferprotectionindietinducedobesemicedespitealteredimmunecellprofilesinthelung
AT hollyacyphert sarscov2mrnavaccinesconferprotectionindietinducedobesemicedespitealteredimmunecellprofilesinthelung
AT emelsenkilic sarscov2mrnavaccinesconferprotectionindietinducedobesemicedespitealteredimmunecellprofilesinthelung
AT mariettebarbier sarscov2mrnavaccinesconferprotectionindietinducedobesemicedespitealteredimmunecellprofilesinthelung
AT fheathdamron sarscov2mrnavaccinesconferprotectionindietinducedobesemicedespitealteredimmunecellprofilesinthelung