Maternal BCG primes for enhanced health benefits in the newborn.

Bacille Calmette-Guérin (BCG) Early-life morbidity and mortality Live-vaccines Maternal BCG priming Non-specific effects of vaccines Vertical priming

Journal

The Journal of infection
ISSN: 1532-2742
Titre abrégé: J Infect
Pays: England
ID NLM: 7908424

Informations de publication

Date de publication:
03 2022
Historique:
received: 05 07 2021
revised: 22 11 2021
accepted: 15 12 2021
pubmed: 28 12 2021
medline: 8 4 2022
entrez: 27 12 2021
Statut: ppublish

Résumé

Bacille Calmette-Guérin (BCG) vaccination lowers the risk of severe infection; we tested whether effects are modulated by maternal BCG in a large cohort of BCG-vaccinated newborns from Guinea-Bissau. Maternal BCG scar status were inspected at enrolment in a BCG trial conducted from 2014 to 17 in Bissau, Guinea-Bissau. We tested associations with background factors for potential confounding; maternal age affected effect estimates >5% and accordingly, all analyses were adjusted for maternal age. Hospitalization data was collected prospectively and assessed in Cox-models providing adjusted Incidence Rate Ratios (aIRRs). In-hospital risk of death (case-fatality) risk was assessed using binomial regression providing adjusted Risk Ratios (aRRs). 60% (6,309/10,598) of mothers had a scar. The maternal-scar/no-scar admission aIRR was 0.96 (0.81-1.14) from 0 to 6 weeks and 1.12 (0.97-1.28) for 6 weeks-3 years. The 6-week in-hospital case-fatality infection aRR was 0.59 (0.34-1.05); 0.40 (0.17-0.91) for males and 0.86 (0.38-1.94) for females. Protection was especially evident against sepsis, the overall 6-week aRR=0.49 (0.26-0.91); no effect was observed for non-infectious deaths or after 6 weeks of age. Effects were similar across BCG strains and multivariate models adjusted for socioeconomic status did not affect estimates. Among BCG-vaccinated newborns, there was a trend for fewer in-hospital deaths from infection associated with maternal BCG priming, especially for males. Providing BCG to adults without a vaccination scar might enhance their offspring's capacity to handle severe infections. Brief 40-word summary: Within a trial comparing BCG strains for their overall effects on morbidity and mortality in Guinea-Bissau, vertical priming with BCG (represented by the maternal BCG scar) was associated with beneficial sex-differential effects on offspring survival.

Identifiants

pubmed: 34958808
pii: S0163-4453(21)00646-0
doi: 10.1016/j.jinf.2021.12.028
pii:
doi:

Substances chimiques

BCG Vaccine 0

Banques de données

ClinicalTrials.gov
['NCT02447536']

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

321-328

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2021. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest At the time the data collection was conducted, several of the authors were affiliated with the Statens Serum Institute (SSI) in Copenhagen which administered, but did not finance, their grants. SSI was a producer of BCG. However, SSI did not fund the vaccines, the study, or the researchers and neither the SSI or funders had any influence on the study design, data collection, analysis, interpretation or writing of the report, nor the decision to submit the paper for publication. None of the authors have any commercial, financial, or personal interests, relationships or other associations that might pose a conflict of interest in relation to this study. Data sharing agreement. Deidentified participant data with a data dictionary can be shared after approval of a data-sharing proposal sent to Professor Christine Stabell Benn (cbenn@health.sdu.dk).

Auteurs

Frederik Schaltz-Buchholzer (F)

Bandim Health Project, INDEPTH Network, Bissau, Guinea-Bissau; Bandim Health Project, OPEN, Institute of Clinical Research, Uni. Southern Denmark and Odense University Hospital, Odense, Denmark. Electronic address: fschaltz-buchholzer@health.sdu.dk.

Christian Bjerregård Øland (C)

Bandim Health Project, INDEPTH Network, Bissau, Guinea-Bissau.

Mike Berendsen (M)

Bandim Health Project, INDEPTH Network, Bissau, Guinea-Bissau; Bandim Health Project, OPEN, Institute of Clinical Research, Uni. Southern Denmark and Odense University Hospital, Odense, Denmark; Department of Internal Medicine, Radboud Centre for Infectious Diseases, Radboud University Medical Centre, Nijmegen, Netherlands.

Morten Bjerregaard-Andersen (M)

Bandim Health Project, INDEPTH Network, Bissau, Guinea-Bissau.

Elise Brenno Stjernholm (EB)

Bandim Health Project, INDEPTH Network, Bissau, Guinea-Bissau.

Christian N Golding (CN)

Bandim Health Project, INDEPTH Network, Bissau, Guinea-Bissau.

Ivan Monteiro (I)

Bandim Health Project, INDEPTH Network, Bissau, Guinea-Bissau.

Peter Aaby (P)

Bandim Health Project, INDEPTH Network, Bissau, Guinea-Bissau.

Christine Stabell Benn (CS)

Bandim Health Project, INDEPTH Network, Bissau, Guinea-Bissau; Bandim Health Project, OPEN, Institute of Clinical Research, Uni. Southern Denmark and Odense University Hospital, Odense, Denmark; Danish Institute of Advanced Science, Uni. Southern Denmark, Odense, Denmark. Electronic address: cbenn@health.sdu.dk.

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