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Published on: February 22, 2019
Clinical evaluation of group A and group C meningococcal polysaccharide vaccines in infants
Insights
Infant meningococcal polysaccharide vaccines (A and C) showed good safety. Antibody responses varied by age, with older infants demonstrating stronger immunity to vaccine A and C.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Meningococcal disease remains a significant public health concern, particularly in infants.
- Polysaccharide vaccines against Neisseria meningitidis serogroups A and C are available, but their efficacy in infants requires careful evaluation.
- Understanding infant immune responses to these vaccines is crucial for optimizing vaccination strategies.
Purpose of the Study:
- To evaluate the safety and immunogenicity of Group A and Group C meningococcal polysaccharide vaccines in infants.
- To determine the factors influencing antibody response, including infant age, vaccine dose, and prior exposure.
- To establish optimal dosing and identify potential limitations for infant vaccination.
Main Methods:
- A total of 908 doses of Group A and C meningococcal polysaccharide vaccines were administered to 396 infants aged 3 to 12 months.
- Local and systemic reactions were monitored post-vaccination.
- Antibody responses (geometric mean concentrations) were measured at various time points and correlated with age, vaccine dose, and prior antigen exposure.
Main Results:
- No significant local or systemic reactions were observed across all vaccine doses and age groups.
- Infant antibody response to Group A vaccine increased significantly with age, with 7- and 12-month-olds showing >90% response rates.
- Group C vaccine elicited a strong response in 3-month-olds, with 100 mcg appearing optimal, but booster doses did not enhance antibody levels.
- Maternal antibodies appeared to suppress responses in younger infants for Group A vaccine.
Conclusions:
- Meningococcal polysaccharide vaccines (A and C) are safe for infants aged 3-12 months.
- Age is a critical factor in achieving adequate antibody responses, particularly for Group A vaccine.
- The 100 mcg dose of Group C vaccine is recommended for primary immunization, while booster responses are limited.
- Further research into optimizing infant vaccination schedules and overcoming maternal antibody interference is warranted.
Abstract:
Group A and group C meningoccal polysaccharide vaccines were evaluated in infants. No significant local or systemic reactions were observed with 908 doses of vaccine given to 396 infants between 3 and 12 mo of age. The antibody response varied with the age of the infant, vaccine dose, molecular weight of vaccine, prior immunization with vaccine, and prior exposure to naturally occurring cross-reactive antigens. Only 7% of 3-mo-old infants had detectable antibody responses to primary immunization with 5-200 mug of A vaccine, presumably because of suppressive effects of high concentrations of maternal anti-A. More than 90% of 7- and 12-mo-old infants responded to A vaccine, achieving geometric mean anti-A concentrations of 0.38 and 0.98 mug/ml, respectively. The dose-response curve was flat between 10 and 200 mug of A vaccine. Geometric mean anti-A concentrations of 2.51 and 4.00 mug/ml were induced in 7- and 12-mo-old infants by booster injections of A vaccine. Approximately 90% of 3-mo-old infants had detectable antibody responses to primary immunization with C vaccine. The 100-mug dose appeared to be optimal, resulting in geometric mean anti-C concentrations of 0.49, 1.55, and 2.64 mug/ml in 3-, 7-, and 12-mo-old infants, respectively. Significant booster responses were not observed with C vaccine. Indeed, except for the 10-mug dose, booster injections of C vaccine in 7- and 12-mo-old infants resulted in lower anti-C concentrations than did primary immunizations.
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