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Multi-component meningococcal serogroup B (MenB)-4C vaccine induces effective opsonophagocytic killing in children with a complement deficiency.
van den Broek, B; van Els, C A C M; Kuipers, B; van Aerde, K; Henriet, S S; de Groot, R; de Jonge, M I; Langereis, J D; van der Flier, M.
Afiliação
  • van den Broek B; Pediatric Infectious Diseases and Immunology, Amalia Children's Hospital, Nijmegen, the Netherlands.
  • van Els CACM; Expertise Center for Immunodeficiency and Autoinflammation (REIA), Radboudumc, Nijmegen, the Netherlands.
  • Kuipers B; Section Pediatric Infectious Diseases, Laboratory of Medical Immunology, Radboud Institute for Molecular Life Sciences, Radboudumc, Nijmegen, the Netherlands.
  • van Aerde K; Radboud Center for Infectious Diseases, Radboudumc, Nijmegen, the Netherlands.
  • Henriet SS; Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, the Netherlands.
  • de Groot R; Centre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, the Netherlands.
  • de Jonge MI; Pediatric Infectious Diseases and Immunology, Amalia Children's Hospital, Nijmegen, the Netherlands.
  • Langereis JD; Expertise Center for Immunodeficiency and Autoinflammation (REIA), Radboudumc, Nijmegen, the Netherlands.
  • van der Flier M; Section Pediatric Infectious Diseases, Laboratory of Medical Immunology, Radboud Institute for Molecular Life Sciences, Radboudumc, Nijmegen, the Netherlands.
Clin Exp Immunol ; 198(3): 381-389, 2019 12.
Article em En | MEDLINE | ID: mdl-31487400
ABSTRACT
Vaccination against meningococcal serogroup B is recommended for patients with a complement deficiency; however, although immunogenicity in this patient group has been shown, efficacy has not yet been established. In this study, we collected serum from children with a complement deficiency in the alternative pathway or in late terminal pathway before and after vaccination with multi-component meningococcal serogroup B (MenB)-4C. MenB-4C is a multi-component, protein-based vaccine against MenB consisting of factor H-binding protein, Neisserial heparin-binding protein, Neisserial adhesion A and outer membrane vesicles containing Porin A. We assessed the vaccine immunogenicity and vaccine-mediated protection by a whole cell enzyme-linked immunosorbent assay with Neisseria meningitidis serogroup B strains H44/76, 5/99 and NZ98/254, which shows that vaccination induced antibody titers against meningococcus. We show that the classical serum bactericidal activity assay with exogenous serum indicates the presence of vaccine-induced antibodies and capacity to activate complement-mediated pathogen lysis. However, in children with a late terminal pathway deficiency, no complement-mediated pathogen lysis was observed when autologous serum was applied in the serum bactericidal activity assay, demonstrating a lack of serum bactericidal activity in children with complement deficiencies. However, MenB-4C vaccination still induced effective complement-dependent opsonophagocytic killing against N. meningitidis serogroup B in reconstituted whole blood with autologous serum from children with an alternative pathway or late terminal pathway deficiency. These findings support the recommendation to vaccinate all complement-deficient children against MenB.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fagocitose / Proteínas Opsonizantes / Vacinas Meningocócicas / Neisseria meningitidis Sorogrupo B / Doenças da Deficiência Hereditária de Complemento / Meningite Meningocócica Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Clin Exp Immunol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fagocitose / Proteínas Opsonizantes / Vacinas Meningocócicas / Neisseria meningitidis Sorogrupo B / Doenças da Deficiência Hereditária de Complemento / Meningite Meningocócica Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Clin Exp Immunol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Holanda