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Published on: November 5, 2019
Meningococcal disease: the advances and challenges of meningococcal disease prevention
1Children's Memorial Hospital, Special Infectious Diseases, Chicago, IL, USA. ryogev@childrensmemorial.org
Insights
Meningococcal vaccines are crucial for preventing severe disease. While some vaccines protect against serogroups A, C, W-135, and Y, challenges remain in protecting infants and against serogroup B, with long-lasting protection still unavailable.
Area of Science:
- Immunology
- Microbiology
- Vaccinology
Background:
- Meningococcal disease, caused by Neisseria meningitidis, presents with rapid onset and high mortality.
- Five serogroups (A, B, C, W-135, Y) cause the majority of meningococcal disease cases globally.
- Infants in developed countries face the highest risk, with a secondary peak in adolescents.
Purpose of the Study:
- To review the current landscape of meningococcal vaccines.
- To identify existing challenges in meningococcal disease prevention through vaccination.
- To highlight areas for future vaccine development.
Main Methods:
- Review of existing literature on meningococcal vaccines.
- Analysis of vaccine efficacy and impact on disease and carriage.
- Identification of gaps in current vaccine technology.
Main Results:
- Polysaccharide vaccines are less effective in young children but reduce carriage in high-risk groups.
- Protein conjugate vaccines (A, C, W-135, Y) broaden protection but their effect on carriage is largely unknown, except for MenC conjugate.
- Outer membrane vesicle vaccines are used for serogroup B in epidemics, but long-lasting protection is lacking.
Conclusions:
- Significant progress has been made in preventing meningococcal disease caused by serogroups A, C, W-135, and Y.
- Developing effective vaccines for infants and against serogroup B remains a critical challenge.
- Further research is needed for vaccines offering long-lasting protection and impacting transmission.
Abstract:
Vaccination as a means to prevent meningococcal disease caused by Neisseria meningitidis is critical given the abrupt onset and rapid progression of this disease. Five serogroups--A, B, C, W-135, and Y--are responsible for the majority of cases. In developed countries, infants have the greatest risk of disease, with a smaller secondary peak observed in late adolescence. Vaccines utilizing the polysaccharide capsule are poorly immunogenic in young children but can reduce the incidence of meningococcal carriage in high risk groups. In contrast, protein conjugate vaccines to polysaccharide capsules A, C, W-135, and Y have broadened the population protection from disease but their effect on meningococcal carriage and transmission is yet unknown except for monovalent meningococcal C conjugate that has been shown to reduce carriage. Challenges remain in providing direct protection to infants and protection against meningococcal B disease. To date, outer membrane vesicle vaccines have been used to control meningococcal B disease in epidemic settings and vaccine candidates against subcapsular antigens are in development, but a vaccine that confers long-lasting protection is unavailable.
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