Immunogenicity of seasonal inactivated influenza and inactivated polio vaccines among children in Senegal: Results from a cluster-randomized trial.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
03 11 2020
Historique:
received: 15 05 2020
revised: 25 08 2020
accepted: 20 09 2020
pubmed: 6 10 2020
medline: 28 4 2021
entrez: 5 10 2020
Statut: ppublish

Résumé

Data on influenza vaccine immunogenicity in children are limited from tropical developing countries. We recently reported significant, moderate effectiveness of a trivalent inactivated influenza vaccine (IIV) in a controlled, cluster-randomized trial in children in rural Senegal during 2009, a year of H3N2 vaccine mismatch (NCT00893906). We report immunogenicity of IIV3 and inactivated polio vaccine (IPV) from that trial. We evaluated hemagglutination inhibition (HAI) and polio antibody titers in response to vaccination of three age groups (6 through 35 months, 3 through 5 years, and 6 through 8 years). As all children were IIV naïve, each received two vaccine doses, although titers were assessed after only the first dose for subjects aged 6 through 8 years. Seroconversion rates (4-fold titer rise or increase from <1:10 to ≥1:40) were 74-87% for A/H1N1, 76-87% for A/H3N2, and 54-79% for B/Yamagata. Seroprotection rates (HAI titer ≥ 1:40) were 79-88% for A/H1N1, 88-96% for A/H3N2, and 52-74% for B/Yamagata. IIV responses were lowest in the youngest age group, and they were comparable between ages 3 through 5 years after two doses and 6 through 8 years after one dose. We found that baseline seropositivity (HAI titer ≥ 1:10) was an effect modifier of IIV response. Using a seroprotective titer (HAI titer ≥ 1:160) recommended for IIV evaluation in children, we found that among subjects who were seropositive at baseline, 69% achieved seroprotection for both A/H1N1 and A/H3N2, while among those who were seronegative at baseline, seroprotection was achieved in 11% for A/H1N1 and 22% for A/H3N2. The IPV group had high baseline polio antibody seropositivity and appropriate responses to vaccination. Our data emphasize the importance of a two-dose IIV3 series in vaccine naïve children. IIV and IPV vaccines were immunogenic in Senegalese children.

Identifiants

pubmed: 33012603
pii: S0264-410X(20)31230-5
doi: 10.1016/j.vaccine.2020.09.059
pmc: PMC7936169
mid: NIHMS1631880
pii:
doi:

Substances chimiques

Antibodies, Viral 0
Influenza Vaccines 0
Vaccines, Inactivated 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

7526-7532

Subventions

Organisme : World Health Organization
ID : 001
Pays : International
Organisme : NIAID NIH HHS
ID : T32 AI007524
Pays : United States
Organisme : NCIRD CDC HHS
ID : U01 IP000174
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Mbayame Niang (M)

National Influenza and Other Respiratory Viruses Center, Institut Pasteur de Dakar, Senegal.

Meagan E Deming (ME)

Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, USA; Institute of Human Virology, University of Maryland School of Medicine, Baltimore, USA.

Deborah Goudiaby (D)

National Influenza and Other Respiratory Viruses Center, Institut Pasteur de Dakar, Senegal.

Ousmane M Diop (OM)

World Health Organization, Geneva, Switzerland.

Ndongo Dia (N)

National Influenza and Other Respiratory Viruses Center, Institut Pasteur de Dakar, Senegal.

Aldiouma Diallo (A)

UMR VITROME, Institut de Recherche Pour le Développement, Dakar, Senegal.

Justin R Ortiz (JR)

Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, USA.

Doudou Diop (D)

PATH, Dakar, Senegal.

Kristen D C Lewis (KDC)

PATH, Seattle, WA, USA.

Kathryn E Lafond (KE)

Influenza Division, Centers for Disease Control and Prevention, Atlanta, GA, USA.

Marc-Alain Widdowson (MA)

Institute of Tropical Medicine, Antwerp, Belgium; Division Global Health Protection, Centers for Disease Control and Prevention, Nairobi, Kenya.

John C Victor (JC)

PATH, Seattle, WA, USA.

Kathleen M Neuzil (KM)

Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, USA. Electronic address: kneuzil@som.umaryland.edu.

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Classifications MeSH