Oral Presentation 21st Lancefield International Symposium for Streptococci and Streptococcal Diseases 2022

Prioritising burden of disease estimation to accelerate group A streptococcal vaccine development: creation of a data purpose framework (#11)

Hannah C Moore 1 , Jeffrey W Cannon 1 , David C Kaslow 2 , Theresa Lamagni 3 , Asha C Bowen 1 4 , Kate M Miller 1 , Thomas Cherian 5 , Chris Van Beneden 6 , Jonathan Carapetis 1 4
  1. Telethon Kids Institute, West Perth, WA, Australia
  2. Path, Seattle, USA
  3. UK Health Security Agency, London, UK
  4. Perth Children's Hospital, Perth, WA, Australia
  5. MMGH Consulting, Geneva, Switzerland
  6. CDC Foundation, Atlanta, USA

Background: Group A Streptococcus (Strep A) has an under-appreciated global burden, despite being identified as a World Health Organization priority vaccine target in 2018. Accurate and robust burden of disease data are now needed to guide vaccine development and implementation decisions.

Methods: Through a Working Group formed with the Strep A Vaccine Global Consortium (SAVAC), we developed an innovative systematic framework outlining priorities and requirements of burden of disease data. Requirements were viewed through four different vaccine evaluation objectives: advocacy; regulatory oversight and licensure; policy and post-licensure evaluation; and post-licensure financing.

Results: Key stakeholders vary for each vaccine objective including funding bodies and advocacy groups; national governments, manufacturers and developers; global, regional and national policy makers and multilateral funders. Data purposes vary from quantifying overall and comparative disease burden across jurisdictions; providing the foundation needed to design and plan clinical trials; measuring population-based vaccine preventable disease burden from specific and non-specific endpoints; and enumerating cost of illness and existing control and prevention activities to assess return on investment decisions. We defined data requirements for eight Strep A endpoints including initial vaccine target conditions, pharyngitis and impetigo. Where possible, we differentiated requirements between high- and low-middle-income countries.

Conclusions: This dynamic framework can be used to identify and prioritise research and surveillance activities addressing knowledge gaps for strep A burden of disease and thus accelerate vaccine development. This framework can also be adapted as vaccine candidates progress through clinical trials and to accelerate development of vaccines targeting other diseases.