Neonatal BCG Vaccination for Prevention of Allergy in Infants: The MIS BAIR Randomised Controlled Trial

Author:

Messina Nicole L.12ORCID,Gardiner Kaya13ORCID,Pittet Laure F.124ORCID,Forbes Emily K.1,Francis Kate L.12ORCID,Freyne Bridget1256,Zufferey Christel1,Abruzzo Veronica1,Morison Clare1,Turner Hannah1,Allen Katrina J.1,Flanagan Katie L.789,Ponsonby Anne‐Louise12ORCID,Robins‐Browne Roy12,Shann Frank2ORCID,Vuillermin Peter11011ORCID,Donath Susan12,Casalaz Dan12,Curtis Nigel123ORCID,

Affiliation:

1. Infectious Diseases, Clinical Epidemiology & Biostatistics Unit Population Allergy, Murdoch Children's Research Institute Parkville Victoria Australia

2. Department of Paediatrics, Department of Microbiology & Immunology The Florey Institute of Neuroscience and Mental Health, The University of Melbourne Parkville Victoria Australia

3. Department of General Medicine, Department of Research Operations, Infectious Diseases Unit The Royal Children's Hospital Parkville Victoria Australia

4. Paediatric Immunology, Vaccinology, Rheumatology and Infectious Diseases Unit Geneva University Hospitals and Faculty of Medicine Geneva Switzerland

5. School of Medicine University College Dublin Ireland

6. Department of Paediatric Infectious Diseases Children's Health Ireland Dublin Ireland

7. School of Medicine University of Tasmania Hobart Tasmania Australia

8. Tasmanian Vaccine Trial Centre, Clifford Craig Foundation Launceston General Hospital Launceston Tasmania Australia

9. School of Health and Biomedical Science RMIT University Melbourne Victoria Australia

10. Institute of Mental and Physical Health and Clinical Translation Deakin University Geelong Victoria Australia

11. Child Health Research Unit Barwon Health Geelong Victoria Australia

12. Neonatal Intensive Care Unit Mercy Hospital for Women Heidelberg Victoria Australia

Abstract

ABSTRACTBackgroundThe beneficial off‐target effects of Bacille Calmette–Guérin (BCG) vaccination potentially include protection against allergy.ObjectiveIn the MIS BAIR trial, we aimed to determine whether neonatal BCG vaccination reduces atopic sensitisation and clinical food allergy in infants.MethodsIn this randomised controlled trial, 1272 neonates were allocated to BCG‐Denmark vaccine (0.05 mL intradermal dose) or no BCG at birth. Randomisation was stratified by recruitment site, mode of delivery and plurality of birth. The primary outcome was the incidence of atopic sensitisation determined by skin prick test at 1 year of age. Food allergy was determined by 3‐monthly online questionnaires and oral food challenges. Data were analysed by intention‐to‐treat using binary regression. Clinicaltrials.gov (NCT01906853).ResultsAtopic sensitisation during the first year of life was 22.9% among infants in the BCG group and 18.9% in the control group (adjusted risk difference (aRD) 3.8% (95% CI −1.5 to 9.1) after multiple imputation). Clinical food allergy was similar between infants in the BCG and control groups (9.8% vs. 9.6%; aRD 0.2, 95% CI −3.4 to 3.8). An interaction was observed between the primary outcome and maternal history of BCG vaccination. No interaction was observed for the additional prespecified potential effect modifiers tested (sex, delivery mode, family history of any allergy, season of birth, hepatitis B vaccination at randomisation, BCG scar and age at BCG administration).Conclusions and Clinical RelevanceNeonatal BCG‐Denmark vaccination does not protect against atopic sensitisation or clinical food allergy in the first year of life.

Publisher

Wiley

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