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Meningococcal B Vaccine Immunogenicity in Children With Defects in Complement and Splenic Function
Federico Martinón-Torres1, Ewa Bernatowska2, Anna Shcherbina3
1Translational Pediatrics and Infectious Diseases, Hospital Clinico Universitario de Santiago de Compostela, Santiago de Compostela, Spain.
The quadrivalent meningococcal serogroup B vaccine (4CMenB) shows similar immunogenicity in healthy children and those with asplenia or splenic dysfunction. Lower immune responses were observed in some complement-deficient children, warranting further surveillance.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- The quadrivalent meningococcal group B vaccine (4CMenB) is recommended for at-risk children, including those with complement deficiencies, asplenia, or splenic dysfunction.
- Limited data exist on the immunogenicity of 4CMenB in these specific pediatric populations.
Purpose of the Study:
- To evaluate the immunogenicity of the 4CMenB vaccine in children with complement deficiencies, asplenia, or splenic dysfunction.
- To compare vaccine responses in these at-risk groups with healthy children.
Main Methods:
- A study involving 239 children aged 2-17 years, including those with complement deficiencies (n=40), asplenia/splenic dysfunction (n=112), and healthy controls (n=87).
- Participants received two doses of 4CMenB, and serum bactericidal activity (SBA) was measured using exogenous and endogenous complement against four Neisseria meningitidis serogroup B strains.
- SBA was assessed at baseline and one month post-vaccination.
Main Results:
- After vaccination, high proportions of participants with asplenia/splenic dysfunction and healthy controls achieved serum bactericidal activity (SBA) titers ≥1:5 against all tested strains using exogenous complement.
- Complement-deficient children showed slightly lower SBA titers compared to controls, particularly those with terminal complement deficiencies or on eculizumab therapy.
- Strain-specific bactericidal activity with endogenous complement was limited in participants with severe complement deficiencies.
Conclusions:
- The 4CMenB vaccine demonstrates comparable immunogenicity in healthy children and those with asplenia or splenic dysfunction.
- A trend towards lower SBA responses was noted in some complement-deficient children, highlighting the need for continued surveillance for vaccine effectiveness in these vulnerable groups.
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