Effect of neonatal BCG vaccination on oral herpes in early childhood: A nested study within a randomised controlled trial
Clinical Snapshot
PICO Framework
| P — Population | 563 children followed for 5 years from birth (44% of 1272 originally randomised in MIS BAIR trial) |
| I — Intervention | Neonatal BCG vaccination |
| C — Comparator | No BCG vaccination (control group) |
| O — Outcomes | Primary: incidence of herpes labialis in first 5 years. Secondary: recurrence rates, time to onset, impact on fluid intake |
Bottom Line
This pilot study suggests neonatal BCG vaccination may reduce herpes labialis recurrence in children, but the evidence is preliminary and limited by substantial methodological weaknesses. The primary outcome (incidence reduction) was not statistically significant, and the study suffered from 56% attrition, lack of virological confirmation, and missing confidence intervals. While the 53% reduction in recurrence rates was statistically significant, this finding requires replication in adequately powered studies with objective outcome measures. The clinical significance remains uncertain given the low baseline incidence of oral herpes in young children. Australian clinicians should await confirmatory evidence before considering BCG for HSV prevention, particularly given the current limited BCG supply and established indications for tuberculosis prevention in high-risk populations.
Key Findings
P Value: p = 0.1 for incidence, p = 0.02 for recurrence
Effect Size: 38% relative risk reduction for incidence (not significant), 53% relative risk reduction for recurrence (significant)
Primary Outcome: Herpes labialis incidence: 5% (BCG) vs 8% (control), 38% relative risk reduction
Nnt Or Sensitivity: Number needed to treat approximately 33 to prevent one case of herpes labialis
Confidence Interval: Not reported
Clinical Application
BCG already available in Australia for high-risk populations; would require policy consideration for broader use Relevant to Australian Indigenous populations and high TB-risk groups already receiving BCG; TGA approval exists for BCG but not for HSV prevention indication Australian newborns in settings where BCG vaccination is being considered
Abstract
BACKGROUND: Bacille Calmette-Guérin (BCG) vaccine, primarily used against tuberculosis, has off-target (non-specific) immunomodulatory effects, including potential protection against recurrences of latent herpes simplex virus (HSV) infections. Recurrent episodes of HSV herpes labialis (oral 'cold sores') affect a substantial proportion of the population, including young children, and there is currently no effective preventive intervention. METHODS: This pilot study, nested within the MIS BAIR randomised controlled trial (RCT), explored whether neonatal BCG vaccination, compared with no BCG vaccination, reduces the incidence and recurrence of herpes labialis during the first five years of life. FINDINGS: Among the 563 children (44% of 1272 randomised) who completed the 5-year follow-up, children in the BCG group were less likely to develop herpes labialis, compared with the control group (5% vs 8%; 38% relative risk reduction, p = 0.1). Risk of recurrence was significantly lower in the BCG group (33% vs. 71%; 53% relative risk reduction, p = 0.02). BCG-vaccinated children also reported a later onset of symptoms and a reduced impact on fluid intake during episodes. INTERPRETATION: This exploratory study suggests a protective role for neonatal BCG against HSV in children. However, its limitations, including its sample size, incomplete follow up and lack of virological confirmation, mean further studies are needed to confirm these findings. FUNDING: National Health and Medical Research Council (NHMRC) of Australia and others, as detailed in the acknowledgements.
References
- 1.Pittet, L. F., Casalaz, D., Donath, S., Gardiner, K., Goodall, C., Flanagan, K. L., Robins-Browne, R., Shann, F., Curtis, N., & Messina, N. L. (2026). Effect of neonatal BCG vaccination on oral herpes in early childhood: A nested study within a randomised controlled trial. Vaccine, Article 128577. https://doi.org/10.1016/j.vaccine.2026.128577
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