DTaP5-IPV-Hib-HepB, a hexavalent vaccine for infants and toddlers

Introduction: Combination vaccines reduce the ‘shot burden’ and simplify the childhood immunization schedule. Only 5-valent DTaP-based vaccines are licensed in the U.S. Areas covered: A new combination vaccine – DTaP5-IPV-Hib-HepB – is described, which induces antibody responses in infants (given in...

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Main Authors: Andrew W. Lee, Emilia Jordanov, Florence Boisnard, Gary S. Marshall
Format: Article
Language:English
Published: Taylor & Francis Group 2017-02-01
Series:Expert Review of Vaccines
Subjects:
Online Access:http://dx.doi.org/10.1080/14760584.2017.1268920
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author Andrew W. Lee
Emilia Jordanov
Florence Boisnard
Gary S. Marshall
author_facet Andrew W. Lee
Emilia Jordanov
Florence Boisnard
Gary S. Marshall
author_sort Andrew W. Lee
collection DOAJ
description Introduction: Combination vaccines reduce the ‘shot burden’ and simplify the childhood immunization schedule. Only 5-valent DTaP-based vaccines are licensed in the U.S. Areas covered: A new combination vaccine – DTaP5-IPV-Hib-HepB – is described, which induces antibody responses in infants (given in different schedules, including a 2, 4, and 6-month schedule) that are similar to the respective component vaccines. The vaccine appears to be safe and would be expected to protect against six diseases: diphtheria, tetanus, pertussis, hepatitis B, H influenzae type b, and polio. Administration is associated with higher rates of mild fever, but without significant safety signals. Expert commentary: Incorporation of this hexavalent vaccine into the U.S. schedule could improve coverage rates and timeliness, and addition to the E.U. market would add depth to the available repertoire of combination vaccines.
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spelling doaj.art-35bede5c3c2746f6a81bdcabdae6e7af2023-09-20T10:18:02ZengTaylor & Francis GroupExpert Review of Vaccines1476-05841744-83952017-02-01162859210.1080/14760584.2017.12689201268920DTaP5-IPV-Hib-HepB, a hexavalent vaccine for infants and toddlersAndrew W. Lee0Emilia Jordanov1Florence Boisnard2Gary S. Marshall3Merck & Co., Inc.Sanofi PasteurSanofi Pasteur MSDUniversity of LouisvilleIntroduction: Combination vaccines reduce the ‘shot burden’ and simplify the childhood immunization schedule. Only 5-valent DTaP-based vaccines are licensed in the U.S. Areas covered: A new combination vaccine – DTaP5-IPV-Hib-HepB – is described, which induces antibody responses in infants (given in different schedules, including a 2, 4, and 6-month schedule) that are similar to the respective component vaccines. The vaccine appears to be safe and would be expected to protect against six diseases: diphtheria, tetanus, pertussis, hepatitis B, H influenzae type b, and polio. Administration is associated with higher rates of mild fever, but without significant safety signals. Expert commentary: Incorporation of this hexavalent vaccine into the U.S. schedule could improve coverage rates and timeliness, and addition to the E.U. market would add depth to the available repertoire of combination vaccines.http://dx.doi.org/10.1080/14760584.2017.1268920diphtheriatetanuspertussispoliohibhepatitis bhexavalentvaccinesafetyimmunogenicitycombination vaccine
spellingShingle Andrew W. Lee
Emilia Jordanov
Florence Boisnard
Gary S. Marshall
DTaP5-IPV-Hib-HepB, a hexavalent vaccine for infants and toddlers
Expert Review of Vaccines
diphtheria
tetanus
pertussis
polio
hib
hepatitis b
hexavalent
vaccine
safety
immunogenicity
combination vaccine
title DTaP5-IPV-Hib-HepB, a hexavalent vaccine for infants and toddlers
title_full DTaP5-IPV-Hib-HepB, a hexavalent vaccine for infants and toddlers
title_fullStr DTaP5-IPV-Hib-HepB, a hexavalent vaccine for infants and toddlers
title_full_unstemmed DTaP5-IPV-Hib-HepB, a hexavalent vaccine for infants and toddlers
title_short DTaP5-IPV-Hib-HepB, a hexavalent vaccine for infants and toddlers
title_sort dtap5 ipv hib hepb a hexavalent vaccine for infants and toddlers
topic diphtheria
tetanus
pertussis
polio
hib
hepatitis b
hexavalent
vaccine
safety
immunogenicity
combination vaccine
url http://dx.doi.org/10.1080/14760584.2017.1268920
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