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Antibody responses after primary immunization in infants born to women receiving a Pertussis-containing vaccine during pregnancy: Single arm observational study with a historical comparator

Antibody responses after primary immunization in infants born to women receiving a Pertussis-containing vaccine during pregnancy: Single arm observational study with a historical comparator
Antibody responses after primary immunization in infants born to women receiving a Pertussis-containing vaccine during pregnancy: Single arm observational study with a historical comparator
Introduction: In England, antenatal pertussis immunization using a tetanus/low-dose diphtheria/5-component acellular-pertussis/inactivated-polio (TdaP5/IPV) vaccine was introduced in October 2012. We assessed infant responses to antigens in the maternal vaccine and to those conjugated to tetanus (TT) or the diphtheria toxin variant, CRM.
Methods: Infants of 141 TdaP5/IPV-vaccinated mothers in Southern England immunized with DTaP5/IPV/Haemophilus influenzae b (Hib-TT) vaccine at 2-3-4 months, 13-valent pneumococcal vaccine (PCV13, CRM-conjugated) at 2-4 months and 1 or 2 meningococcal C vaccine (MCC-CRM- or MCC-TT) doses at 3-4 months had blood samples taken at 2 and/or 5 months of age. Results. Antibody responses to pertussis toxin (PT), filamentous hemagglutinin (FHA), fimbriae 2 + 3 (FIMs), diphtheria, tetanus, Hib, MCC and PCV13 serotypes were compared to responses in a historical cohort of 246 infants born to mothers not vaccinated in pregnancy. Infants had high pertussis antibody concentrations pre-immunization but only PT antibodies increased post-immunization (fold-change, 2.64; 95% confidence interval [CI], 2.12-3.30; P <. 001), whereas FHA antibodies fell (fold-change, 0.56; 95% CI,. 48-.65; P <. 001). Compared with infants of unvaccinated mothers, PT, FHA, and FIMs antibodies were lower post-vaccination, with fold-differences of 0.67 (0.58-0.77; P <. 001), 0.62 (0.54-0.71; P <. 001) and 0.51 (0.42-0.62; P <. 001), respectively. Antibodies to diphtheria and some CRM-conjugated antigens were also lower, although most infants achieved protective thresholds; antibodies to tetanus and Hib were higher. Conclusions. Antenatal pertussis immunization results in high infant pre-immunization antibody concentrations, but blunts subsequent responses to pertussis vaccine and some CRM-conjugated antigens. In countries with no pertussis booster until school age, continued monitoring of protection against pertussis is essential.
conjugate vaccines
1058-4838
1637-1644
Ladhani, Shamez N.
d6111c34-22d1-4ba5-9510-eca5f4e20db8
Andrews, Nick J.
a262c189-ff23-45de-822c-213d6dcedad9
Southern, Jo
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Jones, Christine E.
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Amirthalingam, Gayatri
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Waight, Pauline A.
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England, Anna
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Matheson, Mary
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Bai, Xilian
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Findlow, Helen
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Burbidge, Polly
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Thalasselis, Vasili
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Hallis, Bassam
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Goldblatt, David
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Borrow, Ray
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Heath, Paul T.
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Miller, Elizabeth
180cf79e-2de5-4cc4-bba4-c1610d5b5036
et al.
Ladhani, Shamez N.
d6111c34-22d1-4ba5-9510-eca5f4e20db8
Andrews, Nick J.
a262c189-ff23-45de-822c-213d6dcedad9
Southern, Jo
caf11713-98a0-49c6-a403-b297319aeae3
Jones, Christine E.
48229079-8b58-4dcb-8374-d9481fe7b426
Amirthalingam, Gayatri
483455da-eee7-43d0-9252-1acfad58aa2c
Waight, Pauline A.
31552cca-58bf-453c-b583-8da811d69fee
England, Anna
d843e84f-0d7a-4e4b-901c-e93ee549c865
Matheson, Mary
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Bai, Xilian
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Findlow, Helen
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Burbidge, Polly
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Thalasselis, Vasili
59415110-46cb-490f-bf3d-03e35b608ef3
Hallis, Bassam
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Goldblatt, David
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Borrow, Ray
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Heath, Paul T.
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Miller, Elizabeth
180cf79e-2de5-4cc4-bba4-c1610d5b5036

Ladhani, Shamez N., Andrews, Nick J., Southern, Jo, Jones, Christine E. and Waight, Pauline A. , et al. (2015) Antibody responses after primary immunization in infants born to women receiving a Pertussis-containing vaccine during pregnancy: Single arm observational study with a historical comparator. Clinical Infectious Diseases, 61 (11), 1637-1644. (doi:10.1093/cid/civ695).

Record type: Article

Abstract

Introduction: In England, antenatal pertussis immunization using a tetanus/low-dose diphtheria/5-component acellular-pertussis/inactivated-polio (TdaP5/IPV) vaccine was introduced in October 2012. We assessed infant responses to antigens in the maternal vaccine and to those conjugated to tetanus (TT) or the diphtheria toxin variant, CRM.
Methods: Infants of 141 TdaP5/IPV-vaccinated mothers in Southern England immunized with DTaP5/IPV/Haemophilus influenzae b (Hib-TT) vaccine at 2-3-4 months, 13-valent pneumococcal vaccine (PCV13, CRM-conjugated) at 2-4 months and 1 or 2 meningococcal C vaccine (MCC-CRM- or MCC-TT) doses at 3-4 months had blood samples taken at 2 and/or 5 months of age. Results. Antibody responses to pertussis toxin (PT), filamentous hemagglutinin (FHA), fimbriae 2 + 3 (FIMs), diphtheria, tetanus, Hib, MCC and PCV13 serotypes were compared to responses in a historical cohort of 246 infants born to mothers not vaccinated in pregnancy. Infants had high pertussis antibody concentrations pre-immunization but only PT antibodies increased post-immunization (fold-change, 2.64; 95% confidence interval [CI], 2.12-3.30; P <. 001), whereas FHA antibodies fell (fold-change, 0.56; 95% CI,. 48-.65; P <. 001). Compared with infants of unvaccinated mothers, PT, FHA, and FIMs antibodies were lower post-vaccination, with fold-differences of 0.67 (0.58-0.77; P <. 001), 0.62 (0.54-0.71; P <. 001) and 0.51 (0.42-0.62; P <. 001), respectively. Antibodies to diphtheria and some CRM-conjugated antigens were also lower, although most infants achieved protective thresholds; antibodies to tetanus and Hib were higher. Conclusions. Antenatal pertussis immunization results in high infant pre-immunization antibody concentrations, but blunts subsequent responses to pertussis vaccine and some CRM-conjugated antigens. In countries with no pertussis booster until school age, continued monitoring of protection against pertussis is essential.

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Accepted/In Press date: 8 July 2015
Published date: 1 December 2015
Additional Information: Publisher Copyright:© 2015 The Author 2015. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.
Keywords: conjugate vaccines

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Local EPrints ID: 474820
URI: http://eprints.soton.ac.uk/id/eprint/474820
ISSN: 1058-4838
PURE UUID: 99cc3a77-1746-4dee-ae28-91c1e6132f6e
ORCID for Christine E. Jones: ORCID iD orcid.org/0000-0003-1523-2368

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Date deposited: 03 Mar 2023 17:35
Last modified: 17 Mar 2024 03:45

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Contributors

Author: Shamez N. Ladhani
Author: Nick J. Andrews
Author: Jo Southern
Author: Gayatri Amirthalingam
Author: Pauline A. Waight
Author: Anna England
Author: Mary Matheson
Author: Xilian Bai
Author: Helen Findlow
Author: Polly Burbidge
Author: Vasili Thalasselis
Author: Bassam Hallis
Author: David Goldblatt
Author: Ray Borrow
Author: Paul T. Heath
Author: Elizabeth Miller
Corporate Author: et al.

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