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Group B Streptococcus vaccine development: present status and future considerations, with emphasis on perspectives for low and middle income countries

Globally, group B Streptococcus (GBS) remains the leading cause of sepsis and meningitis in young infants, with its greatest burden in the first 90 days of life. Intrapartum antibiotic prophylaxis (IAP) for women at risk of transmitting GBS to their newborns has been effective in reducing, but not e...

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Autores principales: Kobayashi, Miwako, Vekemans, Johan, Baker, Carol J., Ratner, Adam J., Le Doare, Kirsty, Schrag, Stephanie J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070600/
https://www.ncbi.nlm.nih.gov/pubmed/27803803
http://dx.doi.org/10.12688/f1000research.9363.1
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author Kobayashi, Miwako
Vekemans, Johan
Baker, Carol J.
Ratner, Adam J.
Le Doare, Kirsty
Schrag, Stephanie J.
author_facet Kobayashi, Miwako
Vekemans, Johan
Baker, Carol J.
Ratner, Adam J.
Le Doare, Kirsty
Schrag, Stephanie J.
author_sort Kobayashi, Miwako
collection PubMed
description Globally, group B Streptococcus (GBS) remains the leading cause of sepsis and meningitis in young infants, with its greatest burden in the first 90 days of life. Intrapartum antibiotic prophylaxis (IAP) for women at risk of transmitting GBS to their newborns has been effective in reducing, but not eliminating, the young infant GBS disease burden in many high income countries. However, identification of women at risk and administration of IAP is very difficult in many low and middle income country (LMIC) settings, and is not possible for home deliveries. Immunization of pregnant women with a GBS vaccine represents an alternate pathway to protecting newborns from GBS disease, through the transplacental antibody transfer to the fetus in utero. This approach to prevent GBS disease in young infants is currently under development, and is approaching late stage clinical evaluation. This manuscript includes a review of the natural history of the disease, global disease burden estimates, diagnosis and existing control options in different settings, the biological rationale for a vaccine including previous supportive studies, analysis of current candidates in development, possible correlates of protection and current status of immunogenicity assays. Future potential vaccine development pathways to licensure and use in LMICs, trial design and implementation options are discussed, with the objective to provide a basis for reflection, rather than recommendations.
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spelling pubmed-50706002016-10-31 Group B Streptococcus vaccine development: present status and future considerations, with emphasis on perspectives for low and middle income countries Kobayashi, Miwako Vekemans, Johan Baker, Carol J. Ratner, Adam J. Le Doare, Kirsty Schrag, Stephanie J. F1000Res Review Globally, group B Streptococcus (GBS) remains the leading cause of sepsis and meningitis in young infants, with its greatest burden in the first 90 days of life. Intrapartum antibiotic prophylaxis (IAP) for women at risk of transmitting GBS to their newborns has been effective in reducing, but not eliminating, the young infant GBS disease burden in many high income countries. However, identification of women at risk and administration of IAP is very difficult in many low and middle income country (LMIC) settings, and is not possible for home deliveries. Immunization of pregnant women with a GBS vaccine represents an alternate pathway to protecting newborns from GBS disease, through the transplacental antibody transfer to the fetus in utero. This approach to prevent GBS disease in young infants is currently under development, and is approaching late stage clinical evaluation. This manuscript includes a review of the natural history of the disease, global disease burden estimates, diagnosis and existing control options in different settings, the biological rationale for a vaccine including previous supportive studies, analysis of current candidates in development, possible correlates of protection and current status of immunogenicity assays. Future potential vaccine development pathways to licensure and use in LMICs, trial design and implementation options are discussed, with the objective to provide a basis for reflection, rather than recommendations. F1000Research 2016-09-22 /pmc/articles/PMC5070600/ /pubmed/27803803 http://dx.doi.org/10.12688/f1000research.9363.1 Text en Copyright: © 2016 Kobayashi M et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Kobayashi, Miwako
Vekemans, Johan
Baker, Carol J.
Ratner, Adam J.
Le Doare, Kirsty
Schrag, Stephanie J.
Group B Streptococcus vaccine development: present status and future considerations, with emphasis on perspectives for low and middle income countries
title Group B Streptococcus vaccine development: present status and future considerations, with emphasis on perspectives for low and middle income countries
title_full Group B Streptococcus vaccine development: present status and future considerations, with emphasis on perspectives for low and middle income countries
title_fullStr Group B Streptococcus vaccine development: present status and future considerations, with emphasis on perspectives for low and middle income countries
title_full_unstemmed Group B Streptococcus vaccine development: present status and future considerations, with emphasis on perspectives for low and middle income countries
title_short Group B Streptococcus vaccine development: present status and future considerations, with emphasis on perspectives for low and middle income countries
title_sort group b streptococcus vaccine development: present status and future considerations, with emphasis on perspectives for low and middle income countries
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070600/
https://www.ncbi.nlm.nih.gov/pubmed/27803803
http://dx.doi.org/10.12688/f1000research.9363.1
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