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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.
Abstract:
Group A streptococcus (GAS) is known to cause a broad spectrum of illness, from pharyngitis and impetigo, to autoimmune sequelae such as rheumatic heart disease, and invasive diseases. It is a significant cause of infectious disease morbidity and mortality worldwide, but no efficacious vaccine is currently available. Progress in GAS vaccine development has been hindered by a number of obstacles, including a lack of standardization in immunoassays and the need to define human correlates of protection. In this review, we have examined the current immunoassays used in both GAS and other organisms, and explored the various challenges in their implementation in order to propose potential future directions to identify a correlate of protection and facilitate the development of M protein-based vaccines, which are currently the main GAS vaccine candidates.
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.
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