Meningococcal Serogroup B Disease in Vaccinated Children

Author:

Soler-Garcia Aleix1,Fernández de Sevilla Mariona1234,Abad Raquel5,Esteva Cristina13,Alsina Laia1267,Vázquez Julio5,Muñoz-Almagro Carmen1348,Noguera-Julian Antoni1234

Affiliation:

1. Malalties Infeccioses i Resposta Inflamatòria Sistèmica en Pediatria, Institut de Recerca Pediàtrica, Hospital Sant Joan de Déu, Barcelona, Spain

2. Departament de Pediatria, Universitat de Barcelona, Barcelona, Spain

3. CIBER de Epidemiología y Salud Pública, CIBERESP, Madrid, Spain

4. Red de Investigación Translacional en Infectología Pediátrica, RITIP, Madrid, Spain

5. Unidad de Neisseria, Listeria y Bordetella, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Madrid, Spain

6. Clinical Immunology and Primary Immunodeficiencies Unit, Pediatric Allergy and Clinical Immunology Department, Hospital Sant Joan de Déu, Barcelona, Spain

7. Clinical Immunology Unit Hospital Sant Joan de Déu-Hospital Clínic Barcelona, Barcelona, Spain

8. Departament de Medicina, Universitat Internacional de Catalunya, Barcelona, Spain

Abstract

Abstract Background Neisseria meningitidis serogroup B (MenB) is the most frequent cause of invasive meningococcal disease (IMD) in Spain. The multicomponent vaccine against MenB (4CMenB) was approved in Spain in January 2014. Methods We present 4 cases of children who developed MenB-associated IMD despite previous vaccination with 4CMenB. Extensive immunologic diagnostic work-up was performed in order to rule out any immunodeficiency. Also, molecular characterization of the MenB strain was conducted to determine whether bacterial antigens matched vaccine antigens. Results Among the 4 patients (2 girls), 2 had previous risk factors for IMD (recurrent bacterial meningitis of unknown origin and treatment with eculizumab). All patients developed meningitis, but only 2 developed septic shock; they were all cured without sequelae. No other primary or secondary immunodeficiencies were detected. MenB sequence type 213 was identified in 3 cases. With the exception of neisserial heparin-binding antigen peptide 465 present in 1 isolate, the rest of the isolated strains harbored vaccine antigen variants that did not match antigen variants included in the vaccine. Conclusions We present 4 children who developed MenB-associated IMD despite previous vaccination with 4CMenB. In 2 cases, the antibodies induced by 4CMenB likely were not effective against the isolated strains. A high level of suspicion for IMD seems advisable regardless of the patient’s vaccination history.

Funder

Instituto de Salud Carlos III

Fondo Europeo de Desarrollo Regional

Generalitat de Catalunya

Fundación Godía and CIBER en Epidemiología y Salud Pública

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,General Medicine,Pediatrics, Perinatology and Child Health

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