Correlates of Protection for M Protein-Based Vaccines against Group A Streptococcus

Shu Ki Tsoi1, Pierre R Smeesters2, Hannah R C Frost1

  • 1Group A Streptococcus Research Group, Murdoch Childrens Research Institute, Melbourne, VIC 3052, Australia.

Insights

Group A Streptococcus (GAS) causes various illnesses, but no vaccine exists. This review examines immunoassays and challenges to develop M protein-based GAS vaccines and identify protection correlates.

Area of Science:

  • Microbiology
  • Immunology
  • Vaccinology

Background:

  • Group A Streptococcus (GAS) is a significant global pathogen responsible for diverse infections, ranging from mild pharyngitis to severe invasive diseases and autoimmune complications like rheumatic heart disease.
  • Despite its substantial impact on public health, an effective vaccine against GAS remains unavailable, hindering efforts to control its widespread morbidity and mortality.

Purpose of the Study:

  • To review current immunoassays used for GAS and other pathogens.
  • To identify challenges in implementing these immunoassays and propose future directions.
  • To facilitate the development of M protein-based GAS vaccines by defining correlates of protection.

Main Methods:

  • Comprehensive literature review of existing immunoassays for GAS and related bacterial species.
  • Analysis of challenges and limitations in current immunoassay standardization and application.
  • Exploration of potential strategies for identifying human correlates of protection.

Main Results:

  • Current immunoassays for GAS lack standardization, posing a significant hurdle for vaccine development.
  • Defining reliable correlates of protection is crucial for advancing GAS vaccine efficacy.
  • M protein-based vaccines are the primary candidates, but their development requires improved immunological assays.

Conclusions:

  • Standardization of immunoassays and identification of correlates of protection are critical next steps for developing an efficacious GAS vaccine.
  • Addressing these challenges will accelerate the development of M protein-based vaccines.
  • Further research into immunological responses is needed to overcome existing obstacles in GAS vaccine development.