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Immunogenicity, transplacental transfer of pertussis antibodies and safety following pertussis immunization during pregnancy: Evidence from a randomized, placebo-controlled trial
•A 3-component Tdap vaccine was administered during the third trimester of pregnancy.•This resulted in high levels of pertussis antibodies in newborns’ cord blood.•The Tdap vaccine had a clinically acceptable safety profile in mothers and their fetuses/newborns.•These data support routine maternal T...
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Published in: | Vaccine 2020-02, Vol.38 (8), p.2095-2104 |
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creator | Perrett, Kirsten P. Halperin, Scott A. Nolan, Terry Martínez Pancorbo, Cristina Tapiero, Bruce Martinón-Torres, Federico Stranak, Zbynek Virta, Miia Vanderkooi, Otto G. Kosina, Pavel Encinas Pardilla, Maria Begoña Cristobal García, Ignacio Zuccotti, Gian Vincenzo Kostanyan, Lusine Meyer, Nadia Ceregido, Maria Angeles Cheuvart, Brigitte Kuriyakose, Sherine O. Marcos Fernández, Manuel Rodríguez Zambrano, Miguel Ángel Martín García, Adrián Asenjo de la Fuente, Juan Eloy Camacho Marín, Maria Dolores de la Calle Fernández-Miranda, María Romero Espinar, Yolanda Marchisio, Paola Giovanna Manzoni, Paolo Mesaros, Narcisa |
description | •A 3-component Tdap vaccine was administered during the third trimester of pregnancy.•This resulted in high levels of pertussis antibodies in newborns’ cord blood.•The Tdap vaccine had a clinically acceptable safety profile in mothers and their fetuses/newborns.•These data support routine maternal Tdap vaccination to prevent newborn pertussis disease.
Pertussis immunization during pregnancy is recommended in many countries. Data from large randomized controlled trials are needed to assess the immunogenicity, reactogenicity and safety of this approach.
This phase IV, observer-blind, randomized, placebo-controlled, multicenter trial assessed immunogenicity, transplacental transfer of maternal pertussis antibodies, reactogenicity and safety of a reduced-antigen-content diphtheria-tetanus-three-component acellular pertussis vaccine (Tdap) during pregnancy. Women received Tdap or placebo at 27–36 weeks’ gestation with crossover ≤ 72-hour-postpartum immunization. Immune responses were assessed before the pregnancy dose and 1 month after, and from the umbilical cord at delivery. Superiority (primary objective) was reached if the lower limits of the 95% confidence intervals (CIs) of the pertussis geometric mean concentration (GMC) ratios (Tdap/control) in cord blood were ≥ 1.5. Solicited and unsolicited adverse events (AEs) and pregnancy-/neonate-related AEs of interest were recorded.
687 pregnant women were vaccinated (Tdap: N = 341 control: N = 346). Superiority of the pertussis immune response (maternally transferred pertussis antibodies in cord blood) was demonstrated by the GMC ratios (Tdap/control): 16.1 (95% CI: 13.5–19.2) for anti-filamentous hemagglutinin, 20.7 (15.9–26.9) for anti-pertactin and 8.5 (7.0–10.2) for anti-pertussis toxoid. Rates of pregnancy-/neonate-related AEs of interest, solicited general and unsolicited AEs were similar between groups. None of the serious AEs reported throughout the study were considered related to maternal Tdap vaccination.
Tdap vaccination during pregnancy resulted in high levels of pertussis antibodies in cord blood, was well tolerated and had an acceptable safety profile. This supports the recommendation of Tdap vaccination during pregnancy to prevent early-infant pertussis disease.
Clinical Trial Registration. ClinicalTrials.gov: NCT02377349. |
doi_str_mv | 10.1016/j.vaccine.2019.10.105 |
format | article |
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Pertussis immunization during pregnancy is recommended in many countries. Data from large randomized controlled trials are needed to assess the immunogenicity, reactogenicity and safety of this approach.
This phase IV, observer-blind, randomized, placebo-controlled, multicenter trial assessed immunogenicity, transplacental transfer of maternal pertussis antibodies, reactogenicity and safety of a reduced-antigen-content diphtheria-tetanus-three-component acellular pertussis vaccine (Tdap) during pregnancy. Women received Tdap or placebo at 27–36 weeks’ gestation with crossover ≤ 72-hour-postpartum immunization. Immune responses were assessed before the pregnancy dose and 1 month after, and from the umbilical cord at delivery. Superiority (primary objective) was reached if the lower limits of the 95% confidence intervals (CIs) of the pertussis geometric mean concentration (GMC) ratios (Tdap/control) in cord blood were ≥ 1.5. Solicited and unsolicited adverse events (AEs) and pregnancy-/neonate-related AEs of interest were recorded.
687 pregnant women were vaccinated (Tdap: N = 341 control: N = 346). Superiority of the pertussis immune response (maternally transferred pertussis antibodies in cord blood) was demonstrated by the GMC ratios (Tdap/control): 16.1 (95% CI: 13.5–19.2) for anti-filamentous hemagglutinin, 20.7 (15.9–26.9) for anti-pertactin and 8.5 (7.0–10.2) for anti-pertussis toxoid. Rates of pregnancy-/neonate-related AEs of interest, solicited general and unsolicited AEs were similar between groups. None of the serious AEs reported throughout the study were considered related to maternal Tdap vaccination.
Tdap vaccination during pregnancy resulted in high levels of pertussis antibodies in cord blood, was well tolerated and had an acceptable safety profile. This supports the recommendation of Tdap vaccination during pregnancy to prevent early-infant pertussis disease.
Clinical Trial Registration. ClinicalTrials.gov: NCT02377349.</description><identifier>ISSN: 0264-410X</identifier><identifier>EISSN: 1873-2518</identifier><identifier>DOI: 10.1016/j.vaccine.2019.10.105</identifier><identifier>PMID: 31776029</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Adult formulation acellular pertussis vaccine ; Age ; Antibodies ; Antibodies, Bacterial - blood ; Antigens ; Blood ; Clinical trials ; Confidence intervals ; Cord blood ; Diaries ; Diphtheria ; Diphtheria-Tetanus-acellular Pertussis Vaccines - administration & dosage ; Diphtheria-Tetanus-acellular Pertussis Vaccines - adverse effects ; Female ; Gestation ; Hemagglutinins ; Humans ; Immune response ; Immune system ; Immunity, Maternally-Acquired ; Immunization ; Immunogenicity ; Immunoglobulins ; Infant, Newborn ; Laboratories ; Maternal Exposure ; Maternal immunization ; Mothers ; Objectives ; Pertussis ; Postpartum ; Pregnancy ; Randomization ; Safety ; Single-Blind Method ; Tdap ; Tetanus ; Umbilical cord ; Vaccination ; Vaccines ; Whooping cough ; Whooping Cough - prevention & control</subject><ispartof>Vaccine, 2020-02, Vol.38 (8), p.2095-2104</ispartof><rights>2019</rights><rights>Copyright © 2019. Published by Elsevier Ltd.</rights><rights>Copyright Elsevier Limited Feb 18, 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-854c016e0894dac8939eb2748b5954bc1e437f81edec398410995891ea3523ff3</citedby><cites>FETCH-LOGICAL-c440t-854c016e0894dac8939eb2748b5954bc1e437f81edec398410995891ea3523ff3</cites><orcidid>0000-0001-6018-3863 ; 0000-0002-7042-5384 ; 0000-0001-6166-3842</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31776029$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Perrett, Kirsten P.</creatorcontrib><creatorcontrib>Halperin, Scott A.</creatorcontrib><creatorcontrib>Nolan, Terry</creatorcontrib><creatorcontrib>Martínez Pancorbo, Cristina</creatorcontrib><creatorcontrib>Tapiero, Bruce</creatorcontrib><creatorcontrib>Martinón-Torres, Federico</creatorcontrib><creatorcontrib>Stranak, Zbynek</creatorcontrib><creatorcontrib>Virta, Miia</creatorcontrib><creatorcontrib>Vanderkooi, Otto G.</creatorcontrib><creatorcontrib>Kosina, Pavel</creatorcontrib><creatorcontrib>Encinas Pardilla, Maria Begoña</creatorcontrib><creatorcontrib>Cristobal García, Ignacio</creatorcontrib><creatorcontrib>Zuccotti, Gian Vincenzo</creatorcontrib><creatorcontrib>Kostanyan, Lusine</creatorcontrib><creatorcontrib>Meyer, Nadia</creatorcontrib><creatorcontrib>Ceregido, Maria Angeles</creatorcontrib><creatorcontrib>Cheuvart, Brigitte</creatorcontrib><creatorcontrib>Kuriyakose, Sherine O.</creatorcontrib><creatorcontrib>Marcos Fernández, Manuel</creatorcontrib><creatorcontrib>Rodríguez Zambrano, Miguel Ángel</creatorcontrib><creatorcontrib>Martín García, Adrián</creatorcontrib><creatorcontrib>Asenjo de la Fuente, Juan Eloy</creatorcontrib><creatorcontrib>Camacho Marín, Maria Dolores</creatorcontrib><creatorcontrib>de la Calle Fernández-Miranda, María</creatorcontrib><creatorcontrib>Romero Espinar, Yolanda</creatorcontrib><creatorcontrib>Marchisio, Paola Giovanna</creatorcontrib><creatorcontrib>Manzoni, Paolo</creatorcontrib><creatorcontrib>Mesaros, Narcisa</creatorcontrib><title>Immunogenicity, transplacental transfer of pertussis antibodies and safety following pertussis immunization during pregnancy: Evidence from a randomized, placebo-controlled trial</title><title>Vaccine</title><addtitle>Vaccine</addtitle><description>•A 3-component Tdap vaccine was administered during the third trimester of pregnancy.•This resulted in high levels of pertussis antibodies in newborns’ cord blood.•The Tdap vaccine had a clinically acceptable safety profile in mothers and their fetuses/newborns.•These data support routine maternal Tdap vaccination to prevent newborn pertussis disease.
Pertussis immunization during pregnancy is recommended in many countries. Data from large randomized controlled trials are needed to assess the immunogenicity, reactogenicity and safety of this approach.
This phase IV, observer-blind, randomized, placebo-controlled, multicenter trial assessed immunogenicity, transplacental transfer of maternal pertussis antibodies, reactogenicity and safety of a reduced-antigen-content diphtheria-tetanus-three-component acellular pertussis vaccine (Tdap) during pregnancy. Women received Tdap or placebo at 27–36 weeks’ gestation with crossover ≤ 72-hour-postpartum immunization. Immune responses were assessed before the pregnancy dose and 1 month after, and from the umbilical cord at delivery. Superiority (primary objective) was reached if the lower limits of the 95% confidence intervals (CIs) of the pertussis geometric mean concentration (GMC) ratios (Tdap/control) in cord blood were ≥ 1.5. Solicited and unsolicited adverse events (AEs) and pregnancy-/neonate-related AEs of interest were recorded.
687 pregnant women were vaccinated (Tdap: N = 341 control: N = 346). Superiority of the pertussis immune response (maternally transferred pertussis antibodies in cord blood) was demonstrated by the GMC ratios (Tdap/control): 16.1 (95% CI: 13.5–19.2) for anti-filamentous hemagglutinin, 20.7 (15.9–26.9) for anti-pertactin and 8.5 (7.0–10.2) for anti-pertussis toxoid. Rates of pregnancy-/neonate-related AEs of interest, solicited general and unsolicited AEs were similar between groups. None of the serious AEs reported throughout the study were considered related to maternal Tdap vaccination.
Tdap vaccination during pregnancy resulted in high levels of pertussis antibodies in cord blood, was well tolerated and had an acceptable safety profile. This supports the recommendation of Tdap vaccination during pregnancy to prevent early-infant pertussis disease.
Clinical Trial Registration. ClinicalTrials.gov: NCT02377349.</description><subject>Adult formulation acellular pertussis vaccine</subject><subject>Age</subject><subject>Antibodies</subject><subject>Antibodies, Bacterial - blood</subject><subject>Antigens</subject><subject>Blood</subject><subject>Clinical trials</subject><subject>Confidence intervals</subject><subject>Cord blood</subject><subject>Diaries</subject><subject>Diphtheria</subject><subject>Diphtheria-Tetanus-acellular Pertussis Vaccines - administration & dosage</subject><subject>Diphtheria-Tetanus-acellular Pertussis Vaccines - adverse effects</subject><subject>Female</subject><subject>Gestation</subject><subject>Hemagglutinins</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunity, Maternally-Acquired</subject><subject>Immunization</subject><subject>Immunogenicity</subject><subject>Immunoglobulins</subject><subject>Infant, Newborn</subject><subject>Laboratories</subject><subject>Maternal Exposure</subject><subject>Maternal immunization</subject><subject>Mothers</subject><subject>Objectives</subject><subject>Pertussis</subject><subject>Postpartum</subject><subject>Pregnancy</subject><subject>Randomization</subject><subject>Safety</subject><subject>Single-Blind Method</subject><subject>Tdap</subject><subject>Tetanus</subject><subject>Umbilical cord</subject><subject>Vaccination</subject><subject>Vaccines</subject><subject>Whooping cough</subject><subject>Whooping Cough - prevention & 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transplacental transfer of pertussis antibodies and safety following pertussis immunization during pregnancy: Evidence from a randomized, placebo-controlled trial</title><author>Perrett, Kirsten P. ; Halperin, Scott A. ; Nolan, Terry ; Martínez Pancorbo, Cristina ; Tapiero, Bruce ; Martinón-Torres, Federico ; Stranak, Zbynek ; Virta, Miia ; Vanderkooi, Otto G. ; Kosina, Pavel ; Encinas Pardilla, Maria Begoña ; Cristobal García, Ignacio ; Zuccotti, Gian Vincenzo ; Kostanyan, Lusine ; Meyer, Nadia ; Ceregido, Maria Angeles ; Cheuvart, Brigitte ; Kuriyakose, Sherine O. ; Marcos Fernández, Manuel ; Rodríguez Zambrano, Miguel Ángel ; Martín García, Adrián ; Asenjo de la Fuente, Juan Eloy ; Camacho Marín, Maria Dolores ; de la Calle Fernández-Miranda, María ; Romero Espinar, Yolanda ; Marchisio, Paola Giovanna ; Manzoni, Paolo ; Mesaros, 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María</creatorcontrib><creatorcontrib>Romero Espinar, Yolanda</creatorcontrib><creatorcontrib>Marchisio, Paola Giovanna</creatorcontrib><creatorcontrib>Manzoni, Paolo</creatorcontrib><creatorcontrib>Mesaros, Narcisa</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing & Allied Health Database</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest_Health & Medical 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Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>ProQuest_Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><jtitle>Vaccine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Perrett, Kirsten P.</au><au>Halperin, Scott A.</au><au>Nolan, Terry</au><au>Martínez Pancorbo, Cristina</au><au>Tapiero, Bruce</au><au>Martinón-Torres, Federico</au><au>Stranak, Zbynek</au><au>Virta, Miia</au><au>Vanderkooi, Otto G.</au><au>Kosina, Pavel</au><au>Encinas Pardilla, Maria Begoña</au><au>Cristobal García, Ignacio</au><au>Zuccotti, Gian Vincenzo</au><au>Kostanyan, Lusine</au><au>Meyer, Nadia</au><au>Ceregido, Maria Angeles</au><au>Cheuvart, Brigitte</au><au>Kuriyakose, Sherine O.</au><au>Marcos Fernández, Manuel</au><au>Rodríguez Zambrano, Miguel Ángel</au><au>Martín García, Adrián</au><au>Asenjo de la Fuente, Juan Eloy</au><au>Camacho Marín, Maria Dolores</au><au>de la Calle Fernández-Miranda, María</au><au>Romero Espinar, Yolanda</au><au>Marchisio, Paola Giovanna</au><au>Manzoni, Paolo</au><au>Mesaros, Narcisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunogenicity, transplacental transfer of pertussis antibodies and safety following pertussis immunization during pregnancy: Evidence from a randomized, placebo-controlled trial</atitle><jtitle>Vaccine</jtitle><addtitle>Vaccine</addtitle><date>2020-02-18</date><risdate>2020</risdate><volume>38</volume><issue>8</issue><spage>2095</spage><epage>2104</epage><pages>2095-2104</pages><issn>0264-410X</issn><eissn>1873-2518</eissn><abstract>•A 3-component Tdap vaccine was administered during the third trimester of pregnancy.•This resulted in high levels of pertussis antibodies in newborns’ cord blood.•The Tdap vaccine had a clinically acceptable safety profile in mothers and their fetuses/newborns.•These data support routine maternal Tdap vaccination to prevent newborn pertussis disease.
Pertussis immunization during pregnancy is recommended in many countries. Data from large randomized controlled trials are needed to assess the immunogenicity, reactogenicity and safety of this approach.
This phase IV, observer-blind, randomized, placebo-controlled, multicenter trial assessed immunogenicity, transplacental transfer of maternal pertussis antibodies, reactogenicity and safety of a reduced-antigen-content diphtheria-tetanus-three-component acellular pertussis vaccine (Tdap) during pregnancy. Women received Tdap or placebo at 27–36 weeks’ gestation with crossover ≤ 72-hour-postpartum immunization. Immune responses were assessed before the pregnancy dose and 1 month after, and from the umbilical cord at delivery. Superiority (primary objective) was reached if the lower limits of the 95% confidence intervals (CIs) of the pertussis geometric mean concentration (GMC) ratios (Tdap/control) in cord blood were ≥ 1.5. Solicited and unsolicited adverse events (AEs) and pregnancy-/neonate-related AEs of interest were recorded.
687 pregnant women were vaccinated (Tdap: N = 341 control: N = 346). Superiority of the pertussis immune response (maternally transferred pertussis antibodies in cord blood) was demonstrated by the GMC ratios (Tdap/control): 16.1 (95% CI: 13.5–19.2) for anti-filamentous hemagglutinin, 20.7 (15.9–26.9) for anti-pertactin and 8.5 (7.0–10.2) for anti-pertussis toxoid. Rates of pregnancy-/neonate-related AEs of interest, solicited general and unsolicited AEs were similar between groups. None of the serious AEs reported throughout the study were considered related to maternal Tdap vaccination.
Tdap vaccination during pregnancy resulted in high levels of pertussis antibodies in cord blood, was well tolerated and had an acceptable safety profile. This supports the recommendation of Tdap vaccination during pregnancy to prevent early-infant pertussis disease.
Clinical Trial Registration. ClinicalTrials.gov: NCT02377349.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>31776029</pmid><doi>10.1016/j.vaccine.2019.10.105</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-6018-3863</orcidid><orcidid>https://orcid.org/0000-0002-7042-5384</orcidid><orcidid>https://orcid.org/0000-0001-6166-3842</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0264-410X |
ispartof | Vaccine, 2020-02, Vol.38 (8), p.2095-2104 |
issn | 0264-410X 1873-2518 |
language | eng |
recordid | cdi_proquest_journals_2353954475 |
source | ScienceDirect Journals |
subjects | Adult formulation acellular pertussis vaccine Age Antibodies Antibodies, Bacterial - blood Antigens Blood Clinical trials Confidence intervals Cord blood Diaries Diphtheria Diphtheria-Tetanus-acellular Pertussis Vaccines - administration & dosage Diphtheria-Tetanus-acellular Pertussis Vaccines - adverse effects Female Gestation Hemagglutinins Humans Immune response Immune system Immunity, Maternally-Acquired Immunization Immunogenicity Immunoglobulins Infant, Newborn Laboratories Maternal Exposure Maternal immunization Mothers Objectives Pertussis Postpartum Pregnancy Randomization Safety Single-Blind Method Tdap Tetanus Umbilical cord Vaccination Vaccines Whooping cough Whooping Cough - prevention & control |
title | Immunogenicity, transplacental transfer of pertussis antibodies and safety following pertussis immunization during pregnancy: Evidence from a randomized, placebo-controlled trial |
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