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Abstract

Models of Vaccine Finance and Their Potential Application to Group A Streptococcus Vaccines †

1
Department of Economics and Accounting, College of the Holy Cross, Worcester, MA 01610, USA
2
Department of Global Health and Population, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA
*
Author to whom correspondence should be addressed.
Presented at the 22nd Lancefield International Symposium on Streptococci and Streptococcal Diseases, Brisbane, Australia, 1–5 June 2025.
Proceedings 2025, 124(1), 1; https://doi.org/10.3390/proceedings2025124001
Published: 4 August 2025
Background: Group A Streptococcus (GAS) leads to an estimated 600,000 deaths and 600 million cases of pharyngitis per year. There is significant interest in GAS vaccine development. However, without a clear market for such a vaccine in high-income countries, the mechanism to finance it is unclear. Methods: We consider three models of vaccine finance: industry, government financing, and philanthropic funding. We conduct a literature review to determine how existing vaccines have been financed. We then collect data on vaccine R&D funding, prices, coverage rates, and disease burdens. We analyze the data to show how disease burdens are associated with funding models and how funding models relate to coverage rates and prices. Results: Diseases with disproportionate burdens in high-income countries attract more industry funding and have higher vaccine prices and lower coverage rates. Diseases with mixed burdens (a significant burden in high-income and low-income countries, or mostly middle-income countries) attract more public financing. Diseases with exclusively low-income burdens have relied heavily on philanthropic funding. We illustrate these results using the example of the Pneumococcal, RSV, and HPV vaccines, which received substantial industry funding and had a substantial disease burden in high-income countries. Meningococcal disease and Hepatitis B are examples of vaccines with mixed disease burdens and substantial public support for vaccine development. Finally, the development of the Malaria vaccine is a model of philanthropic funding. Conclusion: Like Meningococcal disease and Hepatitis B, GAS has a mixed disease burden. Therefore, it is a prime candidate for government support through a phase three trial and the approval of a vaccine.

Author Contributions

D.E.B. and D.T. designed the analysis. D.T. conducted the analysis and wrote the first version of the abstract. All authors critically evaluated the methodology and results and reviewed and edited the abstract. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the International Vaccine Institute (IVI) via grants from the Leducq Foundation [RHD24VAC01], Wellcome Trust [227524/Z/23/Z] and Open Philanthropy [“SAVAC 2.0 project to accelerate the development of a vaccine against Group A Streptococcus”].

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data were created or analyzed in this study. Data sharing is not applicable to this article.

Conflicts of Interest

The authors declare no conflict of interest.
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Share and Cite

MDPI and ACS Style

Tortorice, D.; Bloom, D.E. Models of Vaccine Finance and Their Potential Application to Group A Streptococcus Vaccines. Proceedings 2025, 124, 1. https://doi.org/10.3390/proceedings2025124001

AMA Style

Tortorice D, Bloom DE. Models of Vaccine Finance and Their Potential Application to Group A Streptococcus Vaccines. Proceedings. 2025; 124(1):1. https://doi.org/10.3390/proceedings2025124001

Chicago/Turabian Style

Tortorice, Daniel, and David E. Bloom. 2025. "Models of Vaccine Finance and Their Potential Application to Group A Streptococcus Vaccines" Proceedings 124, no. 1: 1. https://doi.org/10.3390/proceedings2025124001

APA Style

Tortorice, D., & Bloom, D. E. (2025). Models of Vaccine Finance and Their Potential Application to Group A Streptococcus Vaccines. Proceedings, 124(1), 1. https://doi.org/10.3390/proceedings2025124001

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