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Short-term and long-term antibody response by mice after immunization against Neisseria meningitidis B or diphtheria toxoid

Serogroup B Neisseria meningitidis (MenB) is a major cause of invasive disease in early childhood worldwide. The only MenB vaccine available in Brazil was produced in Cuba and has shown unsatisfactory efficacy when used to immunize millions of children in Brazil. In the present study, we compared th...

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Autores principales: Silva, G.P., Cruz, S.C., Cruz, A.C., Milagres, L.G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854364/
https://www.ncbi.nlm.nih.gov/pubmed/23369971
http://dx.doi.org/10.1590/1414-431X20122556
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author Silva, G.P.
Cruz, S.C.
Cruz, A.C.
Milagres, L.G.
author_facet Silva, G.P.
Cruz, S.C.
Cruz, A.C.
Milagres, L.G.
author_sort Silva, G.P.
collection PubMed
description Serogroup B Neisseria meningitidis (MenB) is a major cause of invasive disease in early childhood worldwide. The only MenB vaccine available in Brazil was produced in Cuba and has shown unsatisfactory efficacy when used to immunize millions of children in Brazil. In the present study, we compared the specific functional antibody responses evoked by the Cuban MenB vaccine with a standard vaccine against diphtheria (DTP: diphtheria, tetanus, pertussis) after primary immunization and boosting of mice. The peak of bactericidal and opsonic antibody titers to MenB and of neutralizing antibodies to diphtheria toxoid (DT) was reached after triple immunization with the MenB vaccine or DTP vaccine, respectively. However, 4 months after immunization, protective DT antibody levels were present in all DTP-vaccinated mice but in only 20% of the mice immunized against MenB. After 6 months of primary immunization, about 70% of animals still had protective neutralizing DT antibodies, but none had significant bactericidal antibodies to MenB. The booster doses of DTP or MenB vaccines produced a significant antibody recall response, suggesting that both vaccines were able to generate and maintain memory B cells during the period studied (6 months post-triple immunization). Therefore, due to the short duration of serological memory induced by the MenB vaccine (VA-MENGOC-BC(®) vaccine), its use should be restricted to outbreaks of meningococcal disease.
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spelling pubmed-38543642013-12-16 Short-term and long-term antibody response by mice after immunization against Neisseria meningitidis B or diphtheria toxoid Silva, G.P. Cruz, S.C. Cruz, A.C. Milagres, L.G. Braz J Med Biol Res Biomedical Sciences Serogroup B Neisseria meningitidis (MenB) is a major cause of invasive disease in early childhood worldwide. The only MenB vaccine available in Brazil was produced in Cuba and has shown unsatisfactory efficacy when used to immunize millions of children in Brazil. In the present study, we compared the specific functional antibody responses evoked by the Cuban MenB vaccine with a standard vaccine against diphtheria (DTP: diphtheria, tetanus, pertussis) after primary immunization and boosting of mice. The peak of bactericidal and opsonic antibody titers to MenB and of neutralizing antibodies to diphtheria toxoid (DT) was reached after triple immunization with the MenB vaccine or DTP vaccine, respectively. However, 4 months after immunization, protective DT antibody levels were present in all DTP-vaccinated mice but in only 20% of the mice immunized against MenB. After 6 months of primary immunization, about 70% of animals still had protective neutralizing DT antibodies, but none had significant bactericidal antibodies to MenB. The booster doses of DTP or MenB vaccines produced a significant antibody recall response, suggesting that both vaccines were able to generate and maintain memory B cells during the period studied (6 months post-triple immunization). Therefore, due to the short duration of serological memory induced by the MenB vaccine (VA-MENGOC-BC(®) vaccine), its use should be restricted to outbreaks of meningococcal disease. Associação Brasileira de Divulgação Científica 2013-02-01 /pmc/articles/PMC3854364/ /pubmed/23369971 http://dx.doi.org/10.1590/1414-431X20122556 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Biomedical Sciences
Silva, G.P.
Cruz, S.C.
Cruz, A.C.
Milagres, L.G.
Short-term and long-term antibody response by mice after immunization against Neisseria meningitidis B or diphtheria toxoid
title Short-term and long-term antibody response by mice after immunization against Neisseria meningitidis B or diphtheria toxoid
title_full Short-term and long-term antibody response by mice after immunization against Neisseria meningitidis B or diphtheria toxoid
title_fullStr Short-term and long-term antibody response by mice after immunization against Neisseria meningitidis B or diphtheria toxoid
title_full_unstemmed Short-term and long-term antibody response by mice after immunization against Neisseria meningitidis B or diphtheria toxoid
title_short Short-term and long-term antibody response by mice after immunization against Neisseria meningitidis B or diphtheria toxoid
title_sort short-term and long-term antibody response by mice after immunization against neisseria meningitidis b or diphtheria toxoid
topic Biomedical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854364/
https://www.ncbi.nlm.nih.gov/pubmed/23369971
http://dx.doi.org/10.1590/1414-431X20122556
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