Antibody persistence in pre-school children after hexavalent vaccine infant primary and booster administration

Objective: Antibody persistence evaluation for all antigens of a fully liquid DTaP-IPV-HB-PRP~T vaccine at 3.5 and 4.5 y of age following different primary series and booster schedules in South Africa and Latin America. Methods: Participants had completed one of two previous studies (Study 1-South A...

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Main Authors: Shabir A. Madhi, Pío López, Betzana Zambrano, Emilia Jordanov, Siham B’Chir, Fernando Noriega, Emmanuel Feroldi
Format: Article
Language:English
Published: Taylor & Francis Group 2019-03-01
Series:Human Vaccines & Immunotherapeutics
Subjects:
Online Access:http://dx.doi.org/10.1080/21645515.2018.1546524
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author Shabir A. Madhi
Pío López
Betzana Zambrano
Emilia Jordanov
Siham B’Chir
Fernando Noriega
Emmanuel Feroldi
author_facet Shabir A. Madhi
Pío López
Betzana Zambrano
Emilia Jordanov
Siham B’Chir
Fernando Noriega
Emmanuel Feroldi
author_sort Shabir A. Madhi
collection DOAJ
description Objective: Antibody persistence evaluation for all antigens of a fully liquid DTaP-IPV-HB-PRP~T vaccine at 3.5 and 4.5 y of age following different primary series and booster schedules in South Africa and Latin America. Methods: Participants had completed one of two previous studies (Study 1-South Africa; Study 2-Latin America). In Study 1, participants who had not received HB vaccine at birth received a 6–10-14 week primary series of DTaP-IPV-HB-PRP~T or DTwP/PRP~T-Hib+HB+OPV and a third group who had received HB vaccine at birth received a 6–10-14 week primary series of DTaP-IPV-HB-PRP~T; all received a booster (15–18 months) of the primary series vaccine(s) except for HB in the DTwP/PRP~T-Hib group. In Study 2, participants received HB vaccine at birth, a 2–4-6 month primary series of DTaP-IPV-HB-PRP~T or DTaP-HB-IPV//PRP~T, and a DTaP-IPV-HB-PRP~T or DTaP-HB-IPV//PRP~T booster (12–24 months). Participants were followed up at 3.5 and 4.5 y of age for antibody persistence. Results: Approximately 80% of eligible participants were assessed. In Study 1, a birth dose of HB increased anti-HBs persistence (≥10 mIU/mL) following DTaP-IPV-HB-PRP~T primary and booster vaccination from 76.3% to 96.1% at 3.5 y of age and from 73.3% to 96.1% at 4.5 y of age; in Study 2, anti-HBs persistence was high and similar in each group. For the other antigens, there were no differences between groups or studies at 3.5 or 4.5 y. Conclusion: Good persistence of antibodies to each antigen in the DTaP-IPV-HB-PRP~T vaccine up to pre-school age, irrespective of the vaccination schedule during the first 2 y of life.
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spelling doaj.art-72a4084b7ffa4c37a98eb077503572dd2023-09-22T08:38:24ZengTaylor & Francis GroupHuman Vaccines & Immunotherapeutics2164-55152164-554X2019-03-0115365866810.1080/21645515.2018.15465241546524Antibody persistence in pre-school children after hexavalent vaccine infant primary and booster administrationShabir A. Madhi0Pío López1Betzana Zambrano2Emilia Jordanov3Siham B’Chir4Fernando Noriega5Emmanuel Feroldi6University of the WitwatersrandCentro de Estudios en Infectología PediátricaSanofi PasteurSanofi PasteurSanofi PasteurSanofi PasteurSanofi PasteurObjective: Antibody persistence evaluation for all antigens of a fully liquid DTaP-IPV-HB-PRP~T vaccine at 3.5 and 4.5 y of age following different primary series and booster schedules in South Africa and Latin America. Methods: Participants had completed one of two previous studies (Study 1-South Africa; Study 2-Latin America). In Study 1, participants who had not received HB vaccine at birth received a 6–10-14 week primary series of DTaP-IPV-HB-PRP~T or DTwP/PRP~T-Hib+HB+OPV and a third group who had received HB vaccine at birth received a 6–10-14 week primary series of DTaP-IPV-HB-PRP~T; all received a booster (15–18 months) of the primary series vaccine(s) except for HB in the DTwP/PRP~T-Hib group. In Study 2, participants received HB vaccine at birth, a 2–4-6 month primary series of DTaP-IPV-HB-PRP~T or DTaP-HB-IPV//PRP~T, and a DTaP-IPV-HB-PRP~T or DTaP-HB-IPV//PRP~T booster (12–24 months). Participants were followed up at 3.5 and 4.5 y of age for antibody persistence. Results: Approximately 80% of eligible participants were assessed. In Study 1, a birth dose of HB increased anti-HBs persistence (≥10 mIU/mL) following DTaP-IPV-HB-PRP~T primary and booster vaccination from 76.3% to 96.1% at 3.5 y of age and from 73.3% to 96.1% at 4.5 y of age; in Study 2, anti-HBs persistence was high and similar in each group. For the other antigens, there were no differences between groups or studies at 3.5 or 4.5 y. Conclusion: Good persistence of antibodies to each antigen in the DTaP-IPV-HB-PRP~T vaccine up to pre-school age, irrespective of the vaccination schedule during the first 2 y of life.http://dx.doi.org/10.1080/21645515.2018.1546524fully liquidhexavalentimmunity persistenceinfantprimary seriesboostervaccine
spellingShingle Shabir A. Madhi
Pío López
Betzana Zambrano
Emilia Jordanov
Siham B’Chir
Fernando Noriega
Emmanuel Feroldi
Antibody persistence in pre-school children after hexavalent vaccine infant primary and booster administration
Human Vaccines & Immunotherapeutics
fully liquid
hexavalent
immunity persistence
infant
primary series
booster
vaccine
title Antibody persistence in pre-school children after hexavalent vaccine infant primary and booster administration
title_full Antibody persistence in pre-school children after hexavalent vaccine infant primary and booster administration
title_fullStr Antibody persistence in pre-school children after hexavalent vaccine infant primary and booster administration
title_full_unstemmed Antibody persistence in pre-school children after hexavalent vaccine infant primary and booster administration
title_short Antibody persistence in pre-school children after hexavalent vaccine infant primary and booster administration
title_sort antibody persistence in pre school children after hexavalent vaccine infant primary and booster administration
topic fully liquid
hexavalent
immunity persistence
infant
primary series
booster
vaccine
url http://dx.doi.org/10.1080/21645515.2018.1546524
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