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Updated: Jul 10, 2026

Intranasal Administration of Recombinant Influenza Vaccines in Chimeric Mouse Models to Study Mucosal Immunity
Published on: June 25, 2015
MF59 is a safe and potent vaccine adjuvant for flu vaccines in humans: what did we learn during its development?
1Novartis Vaccines and Diagnostics Inc., Siena, Italy. derek.ohagan@novartis.com
Abstract:
The MF59 adjuvant has been included in a licensed influenza vaccine for a decade. Hence, we have a significant amount of clinical data to establish its potency and safety. We can now reassess our early preclinical studies and determine whether or not they were useful to predict human responses. The main lesson learned is that mouse models can be valuable, but one must ask the right questions and the models must be used appropriately.
Insights
MF59 adjuvant in influenza vaccines is well-established. Early mouse studies can predict human responses if the right questions are asked and models are used appropriately, validating preclinical research.
Area of Science:
- Immunology
- Vaccinology
- Preclinical Research
Background:
- The MF59 adjuvant has been incorporated into a licensed influenza vaccine for ten years.
- Extensive clinical data exist regarding the potency and safety of MF59-adjuvanted vaccines.
Purpose of the Study:
- To reassess early preclinical studies in light of extensive clinical data on MF59.
- To determine the predictive value of preclinical studies for human responses to MF59-adjuvanted vaccines.
Main Methods:
- Review and analysis of existing preclinical (mouse model) data.
- Comparison of preclinical findings with available human clinical data for MF59-adjuvanted influenza vaccines.
Main Results:
- Preclinical mouse models can provide valuable insights into human responses to MF59.
- The utility of mouse models is dependent on asking appropriate research questions.
Conclusions:
- Mouse models are useful for predicting human responses to MF59 adjuvants when employed correctly.
- Appropriate experimental design and questioning are crucial for the successful application of preclinical models in vaccine development.
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