Effectiveness of Seasonal Influenza Vaccination in Children in Senegal During a Year of Vaccine Mismatch: A Cluster-randomized Trial.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
30 10 2019
Historique:
received: 28 06 2018
accepted: 18 01 2019
pubmed: 29 1 2019
medline: 26 9 2020
entrez: 29 1 2019
Statut: ppublish

Résumé

The population effects of influenza vaccination in children have not been extensively studied, especially in tropical, developing countries. In rural Senegal, we assessed the total (primary objective) and indirect effectiveness of a trivalent inactivated influenza vaccine (IIV3). In this double-blind, cluster-randomized trial, villages were randomly allocated (1:1) for the high-coverage vaccination of children aged 6 months through 10 years with either the 2008-09 northern hemisphere IIV3 or an inactivated polio vaccine (IPV). Vaccinees were monitored for serious adverse events. All village residents, vaccinated and unvaccinated, were monitored for signs and symptoms of influenza illness using weekly home visits and surveillance in designated clinics. The primary outcome was all laboratory-confirmed symptomatic influenza. Between 23 May and 11 July 2009, 20 villages were randomized, and 66.5% of age-eligible children were enrolled (3918 in IIV3 villages and 3848 in IPV villages). Follow-up continued until 28 May 2010. There were 4 unrelated serious adverse events identified. Among vaccinees, the total effectiveness against illness caused by the seasonal influenza virus (presumed to all be drifted A/H3N2, based on antigenic characterization data) circulating at high rates among children was 43.6% (95% confidence interval [CI] 18.6-60.9%). The indirect effectiveness against seasonal A/H3N2 was 15.4% (95% CI -22.0 to 41.3%). The total effectiveness against illness caused by the pandemic influenza virus (A/H1N1pdm09) was -52.1% (95% CI -177.2 to 16.6%). IIV3 provided statistically significant, moderate protection to children in Senegal against circulating, pre-2010 seasonal influenza strains, but not against A/H1N1pdm09, which was not included in the vaccine. No indirect effects were measured. Further study in low-resource populations is warranted. NCT00893906.

Sections du résumé

BACKGROUND
The population effects of influenza vaccination in children have not been extensively studied, especially in tropical, developing countries. In rural Senegal, we assessed the total (primary objective) and indirect effectiveness of a trivalent inactivated influenza vaccine (IIV3).
METHODS
In this double-blind, cluster-randomized trial, villages were randomly allocated (1:1) for the high-coverage vaccination of children aged 6 months through 10 years with either the 2008-09 northern hemisphere IIV3 or an inactivated polio vaccine (IPV). Vaccinees were monitored for serious adverse events. All village residents, vaccinated and unvaccinated, were monitored for signs and symptoms of influenza illness using weekly home visits and surveillance in designated clinics. The primary outcome was all laboratory-confirmed symptomatic influenza.
RESULTS
Between 23 May and 11 July 2009, 20 villages were randomized, and 66.5% of age-eligible children were enrolled (3918 in IIV3 villages and 3848 in IPV villages). Follow-up continued until 28 May 2010. There were 4 unrelated serious adverse events identified. Among vaccinees, the total effectiveness against illness caused by the seasonal influenza virus (presumed to all be drifted A/H3N2, based on antigenic characterization data) circulating at high rates among children was 43.6% (95% confidence interval [CI] 18.6-60.9%). The indirect effectiveness against seasonal A/H3N2 was 15.4% (95% CI -22.0 to 41.3%). The total effectiveness against illness caused by the pandemic influenza virus (A/H1N1pdm09) was -52.1% (95% CI -177.2 to 16.6%).
CONCLUSIONS
IIV3 provided statistically significant, moderate protection to children in Senegal against circulating, pre-2010 seasonal influenza strains, but not against A/H1N1pdm09, which was not included in the vaccine. No indirect effects were measured. Further study in low-resource populations is warranted.
CLINICAL TRIALS REGISTRATION
NCT00893906.

Identifiants

pubmed: 30689757
pii: 5303780
doi: 10.1093/cid/ciz066
pmc: PMC6821165
doi:

Substances chimiques

Influenza Vaccines 0
Vaccines, Inactivated 0

Banques de données

ClinicalTrials.gov
['NCT00893906']

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

1780-1788

Subventions

Organisme : NIAID NIH HHS
ID : R37 AI032042
Pays : United States
Organisme : NCIRD CDC HHS
ID : U01 IP000174
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Références

Clin Trials. 2004;1(3):297-305
pubmed: 16279255
Wkly Epidemiol Rec. 2009 Oct 9;84(41):421-31
pubmed: 19817019
Am J Trop Med Hyg. 2000 May;62(5):639-43
pubmed: 11289677
N Engl J Med. 2011 Oct 13;365(15):1406-16
pubmed: 21995388
Lancet Infect Dis. 2017 Sep;17(9):981-989
pubmed: 28522338
J Infect Dis. 2012 Dec 15;206 Suppl 1:S101-7
pubmed: 23169954
N Engl J Med. 2013 Dec 26;369(26):2481-91
pubmed: 24328444
Am J Epidemiol. 2005 Feb 15;161(4):303-6
pubmed: 15692073
Vaccine. 2006 Feb 20;24(8):1047-62
pubmed: 16298026
Epidemiology. 1991 Sep;2(5):331-8
pubmed: 1742381
JAMA. 2010 Mar 10;303(10):943-50
pubmed: 20215608
PLoS One. 2016 Apr 27;11(4):e0153003
pubmed: 27119988
Clin Infect Dis. 2010 Dec 15;51(12):1370-9
pubmed: 21067351
Int J Epidemiol. 2013 Aug;42(4):1002-11
pubmed: 24062286
Lancet Child Adolesc Health. 2018 May;2(5):338-349
pubmed: 30169267
PLoS One. 2018 Feb 21;13(2):e0193263
pubmed: 29466459
Malar J. 2009 Nov 27;8:270
pubmed: 19943921
Hum Vaccin Immunother. 2013 Jul;9(7):1500-11
pubmed: 23732900
Pediatr Clin North Am. 2017 Aug;64(4):911-936
pubmed: 28734518
Euro Surveill. 2016 Oct 20;21(42):
pubmed: 27784531
Lancet Infect Dis. 2016 Sep;16(9):1026-1035
pubmed: 27261067
AIDS. 2013 Jan 28;27(3):369-79
pubmed: 23032417
PLoS Med. 2010 Apr 06;7(4):e1000258
pubmed: 20386731
Lancet Glob Health. 2016 Dec;4(12):e955-e965
pubmed: 27746224
Vaccine. 2015 Nov 25;33(47):6493-8
pubmed: 26319745

Auteurs

Aldiouma Diallo (A)

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

Ousmane M Diop (OM)

Institut Pasteur de Dakar, Senegal.

Doudou Diop (D)

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

Mbayame Nd Niang (MN)

Institut Pasteur de Dakar, Senegal.

Jonathan D Sugimoto (JD)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.

Justin R Ortiz (JR)

Center for Vaccine Development, University of Maryland, Baltimore.

El Hadji Abdourahmane Faye (EHA)

Institut Pasteur de Dakar, Senegal.

Bou Diarra (B)

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

Deborah Goudiaby (D)

Institut Pasteur de Dakar, Senegal.

Kristen D C Lewis (KDC)

PATH, Seattle, Washington.

Shannon L Emery (SL)

Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.

Sahar Z Zangeneh (SZ)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.

Kathryn E Lafond (KE)

Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.

Cheikh Sokhna (C)

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

M Elizabeth Halloran (ME)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Department of Biostatistics, University of Washington, Seattle.

Marc-Alain Widdowson (MA)

Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.

Kathleen M Neuzil (KM)

Center for Vaccine Development, University of Maryland, Baltimore.

John C Victor (JC)

PATH, Seattle, Washington.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH