# Syrian hamsters as an animal model for influenza virus research

> **NIH NIH R01** · UNIVERSITY OF WISCONSIN-MADISON · 2020 · $721,773

## Abstract

PROJECT SUMMARY
 To facilitate NIAID’s strategic plan for the development of a universal influenza vaccine, PAR-19-248 solicits
“Research Projects to Improve the Predictive Value of Animal Models in Recapitulating Human Immunity to
Influenza Infection and Vaccination”. Here, we address some of the major research needs identified in PAR-19-
248 by continuing our development of golden Syrian hamsters (hereafter referred to as hamsters) as an animal
model for influenza virus research. This is based on our previous findings that the composition of influenza virus
receptors in the respiratory tract of hamsters is similar to that in the respiratory tract of humans, and that human
influenza A viruses replicate in the respiratory tract of hamsters, including recent human H3N2 influenza viruses,
which do not replicate efficiently in mice. In Specific Aim 1, we plan to establish an influenza virus aerosol
exposure platform for hamsters. Currently, most influenza virus infection studies entail intranasal virus
inoculation, which is not the natural route of infection (i.e., aerosol exposure). By establishing an aerosol
exposure platform for hamsters, we are addressing a key topic of PAR-19-248. In Specific Aim 2, we will assess
the predictive value of hamsters in simulating the impact of the first exposure to influenza viruses on
subsequent exposures (imprinting). With few exceptions, influenza virus infection and vaccination studies
have been conducted in naïve animals, thus not reflecting the immune status of most humans who have been
exposed to multiple influenza viruses through infections and/or vaccinations. Here, we will sequentially infect
hamsters (via intranasal infection or aerosol exposure) with the same human influenza viruses that caused the
first and second infections in a child (based on clinical samples that we have obtained from a pediatric cohort
study). Hamster and human sera will then be compared for B cell responses to the first and second infections.
In Specific Aim 3, we will assess the predictive value of hamsters in simulating human immune responses
to multiple infections, vaccination, and challenge. Hamsters will be sequentially infected with two different
influenza viruses, and subsequently vaccinated with an inactivated vaccine. The B cell responses elicited will be
compared to those of human samples obtained before and after vaccination with the same vaccine strain that
will be used to vaccinate the hamsters. In another study, hamsters will be sequentially infected with two different
influenza viruses, and subsequently vaccinated with an investigational (potentially broadly protective) vaccine
and challenged with a heterologous virus. The B cell immune responses elicited will be compared with those
from a Phase 2a clinical trial that used the same investigational vaccine and challenge viruses. By leveraging
our preliminary data and our access to human samples, we will address several key topics of PAR-19-248,
including the assess...

## Key facts

- **NIH application ID:** 9949248
- **Project number:** 1R01AI150678-01
- **Recipient organization:** UNIVERSITY OF WISCONSIN-MADISON
- **Principal Investigator:** YOSHIHIRO KAWAOKA
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $721,773
- **Award type:** 1
- **Project period:** 2020-09-02 → 2024-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9949248

## Citation

> US National Institutes of Health, RePORTER application 9949248, Syrian hamsters as an animal model for influenza virus research (1R01AI150678-01). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/9949248. Licensed CC0.

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