Biological sex differences after high and low doses of influenza A virus infection during obesity

Introduction: Obesity is an independent risk factor for influenza A virus (IAV) pathogenesis. In non-obese hosts, following IAV infection, adult females develop more severe disease than males. Limited research on biological sex differences following IAV infection in individuals with obesity forms the basis for this study. Materials and methods: ) of mouse-adapted A/California/04/2009 H1N1 IAV and followed for 21 days post-infection (dpi) for morbidity. Subsets of mice were euthanized at different dpi to measure lung virus titers, histopathological changes, cellular infiltration, and cytokine induction. Results: After a high-dose infection, females with obesity demonstrated shorter median survival time, greater parenchymal inflammation, and heightened induction of inflammatory markers than males with obesity. After a low-dose infection, females more than males, and mice with obesity than the non-obese mice, exhibited severe morbidity. Female mice with obesity exhibited the greatest disease severity, where 25% (2/8) reached humane endpoint. Delayed but persistent inflammatory changes were observed in females with obesity, characterized by relatively lower pathological changes, lesser induction of cytokines and chemokines, and reduced myeloid and lymphoid infiltration in the lungs at 3 dpi, followed by sustained pathological changes and cytokine and chemokine induction up to 21 dpi. Discussion: Our study suggests that the biological sex difference following IAV infection is observed during obesity. Females with obesity experience greater influenza disease severity than males, specially following a low-dose IAV infection, possibly driven by more severe dysregulation of inflammatory responses.

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Publication Details

Journal
Frontiers in Immunology
Published
2026-04-10
DOI
https://doi.org/10.3389/fimmu.2026.1788970
Primary Topic
Influenza Virus Research Studies
Type
article
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article

Biological sex differences after high and low doses of influenza A virus infection during obesity

Saurav Pantha, Tawfik Aboellail, Brian Wolfe, Saranya Vijayakumar et al.
Frontiers in Immunology
Influenza Virus Research Studies
article

Biological sex differences after high and low doses of influenza A virus infection during obesity

Saurav Pantha, Tawfik Aboellail, Brian Wolfe, Saranya Vijayakumar, Santosh Dhakal, Shristy Budha Magar
article en

Abstract

Introduction: Obesity is an independent risk factor for influenza A virus (IAV) pathogenesis. In non-obese hosts, following IAV infection, adult females develop more severe disease than males. Limited research on biological sex differences following IAV infection in individuals with obesity forms the basis for this study. Materials and methods: ) of mouse-adapted A/California/04/2009 H1N1 IAV and followed for 21 days post-infection (dpi) for morbidity. Subsets of mice were euthanized at different dpi to measure lung virus titers, histopathological changes, cellular infiltration, and cytokine induction. Results: After a high-dose infection, females with obesity demonstrated shorter median survival time, greater parenchymal inflammation, and heightened induction of inflammatory markers than males with obesity. After a low-dose infection, females more than males, and mice with obesity than the non-obese mice, exhibited severe morbidity. Female mice with obesity exhibited the greatest disease severity, where 25% (2/8) reached humane endpoint. Delayed but persistent inflammatory changes were observed in females with obesity, characterized by relatively lower pathological changes, lesser induction of cytokines and chemokines, and reduced myeloid and lymphoid infiltration in the lungs at 3 dpi, followed by sustained pathological changes and cytokine and chemokine induction up to 21 dpi. Discussion: Our study suggests that the biological sex difference following IAV infection is observed during obesity. Females with obesity experience greater influenza disease severity than males, specially following a low-dose IAV infection, possibly driven by more severe dysregulation of inflammatory responses.

Frontiers in ImmunologyVol. 17
Kansas State University (US)
Good health and well-being
Openalex Percentile: Top 27%
Influenza Virus Research Studies
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