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Experience and challenges on influenza and pertussis vaccination in pregnant women
Young infants contribute to relatively high burden of vaccine-preventable diseases, including infections by influenza virus and Bordetella pertussis. Vaccination of pregnant women can enhance transplacental transfer of protective antibody to the fetus and protect the infant against disease during th...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6183140/ https://www.ncbi.nlm.nih.gov/pubmed/30024822 http://dx.doi.org/10.1080/21645515.2018.1483810 |
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author | Madhi, Shabir A. Nunes, Marta C. |
author_facet | Madhi, Shabir A. Nunes, Marta C. |
author_sort | Madhi, Shabir A. |
collection | PubMed |
description | Young infants contribute to relatively high burden of vaccine-preventable diseases, including infections by influenza virus and Bordetella pertussis. Vaccination of pregnant women can enhance transplacental transfer of protective antibody to the fetus and protect the infant against disease during the first few months of life. Pregnant women are a priority group for seasonal influenza vaccination, due to third-trimester pregnancy being a risk-factor for severe influenza illness. Furthermore, randomized controlled trials confirmed that influenza vaccination during pregnancy confers protection against influenza-confirmed illness in the women, and their infants up to 3 months of age; and is also associated with 20% reduction in all-cause pneumonia among young-infants. Maternal influenza vaccination might also reduce the risk of low-birth weight, preterm births, and stillbirths however, data on this is conflicting. Vaccination of pregnant women with acellular pertussis vaccines reduces pertussis in their young infants by up to 93%. The increase in specific pertussis antibody among the infants born to vaccinated women might, however, interfere with the active pertussis vaccination of the infant following the primary series of vaccines. The clinical implication of this is yet to be ascertained, particularly since immune responses following the booster vaccine are unaffected. Vaccination of pregnant women with inactivated influenza vaccine and acellular pertussis vaccine have been demonstrated to confer protection to their young infants, and warrants consideration for inclusion into public health immunization programs, including in low and middle income countries. |
format | Online Article Text |
id | pubmed-6183140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-61831402018-10-19 Experience and challenges on influenza and pertussis vaccination in pregnant women Madhi, Shabir A. Nunes, Marta C. Hum Vaccin Immunother Commentary Young infants contribute to relatively high burden of vaccine-preventable diseases, including infections by influenza virus and Bordetella pertussis. Vaccination of pregnant women can enhance transplacental transfer of protective antibody to the fetus and protect the infant against disease during the first few months of life. Pregnant women are a priority group for seasonal influenza vaccination, due to third-trimester pregnancy being a risk-factor for severe influenza illness. Furthermore, randomized controlled trials confirmed that influenza vaccination during pregnancy confers protection against influenza-confirmed illness in the women, and their infants up to 3 months of age; and is also associated with 20% reduction in all-cause pneumonia among young-infants. Maternal influenza vaccination might also reduce the risk of low-birth weight, preterm births, and stillbirths however, data on this is conflicting. Vaccination of pregnant women with acellular pertussis vaccines reduces pertussis in their young infants by up to 93%. The increase in specific pertussis antibody among the infants born to vaccinated women might, however, interfere with the active pertussis vaccination of the infant following the primary series of vaccines. The clinical implication of this is yet to be ascertained, particularly since immune responses following the booster vaccine are unaffected. Vaccination of pregnant women with inactivated influenza vaccine and acellular pertussis vaccine have been demonstrated to confer protection to their young infants, and warrants consideration for inclusion into public health immunization programs, including in low and middle income countries. Taylor & Francis 2018-07-24 /pmc/articles/PMC6183140/ /pubmed/30024822 http://dx.doi.org/10.1080/21645515.2018.1483810 Text en © 2018 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Commentary Madhi, Shabir A. Nunes, Marta C. Experience and challenges on influenza and pertussis vaccination in pregnant women |
title | Experience and challenges on influenza and pertussis vaccination in pregnant women |
title_full | Experience and challenges on influenza and pertussis vaccination in pregnant women |
title_fullStr | Experience and challenges on influenza and pertussis vaccination in pregnant women |
title_full_unstemmed | Experience and challenges on influenza and pertussis vaccination in pregnant women |
title_short | Experience and challenges on influenza and pertussis vaccination in pregnant women |
title_sort | experience and challenges on influenza and pertussis vaccination in pregnant women |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6183140/ https://www.ncbi.nlm.nih.gov/pubmed/30024822 http://dx.doi.org/10.1080/21645515.2018.1483810 |
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