Meningococcal Serogroup B Disease in Vaccinated Children

被引:6
作者
Soler-Garcia, Aleix [1 ]
Fernandez de Sevilla, Mariona [1 ,2 ,3 ,4 ]
Abad, Raquel [5 ]
Esteva, Cristina [1 ,3 ]
Alsina, Laia [1 ,2 ,6 ,7 ]
Vazquez, Julio [5 ]
Munoz-Almagro, Carmen [1 ,3 ,4 ,8 ]
Noguera-Julian, Antoni [1 ,2 ,3 ,4 ]
机构
[1] Hosp St Joan de Deu, Malalties Infeccioses & Resposta Inflamatoria Sis, Inst Recerca Pediat, Barcelona, Spain
[2] Univ Barcelona, Dept Pediat, Barcelona, Spain
[3] CIBERESP, CIBER Epidemiol & Salud Publ, Madrid, Spain
[4] RITIP, Red Invest Translac Infectol Pediat, Madrid, Spain
[5] Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Neisseria Listeria & Bordetella, Madrid, Spain
[6] Hosp St Joan de Deu, Clin Immunol & Primary Immunodeficiencies Unit, Pediat Allergy & Clin Immunol Dept, Barcelona, Spain
[7] Hosp St Joan de Diu, Hosp Clin Barcelona, Clin Immunol Unit, Barcelona, Spain
[8] Univ Int Catalunya, Dept Med, Barcelona, Spain
关键词
child; infant; Neisseria meningitidis group B; sepsis; vaccine; ECULIZUMAB TREATMENT; STRAIN COVERAGE; 4CMENB; IMMUNOGENICITY; CHALLENGES; DIAGNOSIS;
D O I
10.1093/jpids/piz071
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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.
引用
收藏
页码:454 / 459
页数:6
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