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Opsonophagocytic Killing Assay to Assess Immunological Responses Against Bacterial Pathogens
Published on: April 5, 2019
Secondary and apparent primary antibody responses after group A streptococcal vaccination of 21 children
Insights
Group A Streptococcus type 3 M protein vaccination successfully induced type 3 bactericidal antibodies in most children. This study demonstrates the potential of M protein as a vaccine candidate for preventing streptococcal infections.
Area of Science:
- Immunology
- Microbiology
- Vaccinology
Background:
- Group A Streptococcus (GAS) causes various infections.
- Type 3 GAS is a significant pathogen.
- M protein is a key virulence factor and a target for vaccine development.
Purpose of the Study:
- To evaluate the immunogenicity of a partially purified type 3 M protein vaccine in children.
- To assess the antibody response to M protein vaccination in a pediatric population.
Main Methods:
- Twenty-one children received subcutaneous injections of partially purified type 3 M protein vaccine weekly.
- Pre- and post-vaccination sera were analyzed for type 3 bactericidal antibodies.
- Antibody response was categorized as primary or secondary based on prevaccination antibody levels.
Main Results:
- Of 21 children, 20 developed type 3 bactericidal antibodies.
- 13 of 14 children without pre-existing antibodies showed a primary response.
- Secondary responses were observed in 7 children with pre-existing antibodies.
- Reactions were generally mild, with no significant hypersensitivity noted.
Conclusions:
- Partially purified type 3 M protein is immunogenic in children, inducing bactericidal antibodies.
- Vaccination with M protein shows promise for preventing type 3 Group A Streptococcus infections.
- The vaccine was well-tolerated with minimal adverse effects.
Abstract:
A partially purified M protein, extracted from a mouse-virulent strain of type 3, group A streptococcus, was administered subcutaneously in gradually increasing amounts at weekly intervals to 21 children in a Family Program. Seven children with type 3 bactericidal antibody in prevaccination sera showed a secondary response. Of 14 children with no detectable type 3 bactericidal antibody prior to vaccination, 13 developed definite type 3 antibody during or soon after vaccination. This response appeared to be of the primary variety in at least some of the 13 children because (i) the total incidence of antibody response (20 of 21) was greater than can be accounted for by the documented incidence of clinical and subclinical type 3 infections among children of our Family Program during a period of 14 years, (ii) the response in the 13 children with no detectable antibody prior to vaccination was more delayed than in those showing a definite secondary response, and (iii) on the average, the amount of vaccine needed for a response in these 13 children was 15 to 28 times greater than that required for the secondary response. Local skin reactions were variable among the vaccinated children. Systemic reactions were infrequent and not severe. The giving of multiple injections of partially purified M protein did not seem to cause cutaneous hypersensitivity.
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