Why the study?
A novel oral polio vaccine type 2 (nOPV2) has been deployed to interrupt circulating vaccine-derived poliovirus type 2 outbreaks, but its intestinal mucosal immune responses compared with Sabin mOPV2 required evaluation.
Does nOPV2 induce similar intestinal mucosal immune responses compared to mOPV2 in healthy infants, children, and adults?
Does nOPV2 induce similar intestinal mucosal immune responses compared to mOPV2 in healthy infants, children, and adults?
nOPV2 is as effective as mOPV2 in inducing PV2-specific intestinal mucosal immunity, with the strongest responses observed in infants, supporting its use to interrupt circulating vaccine-derived poliovirus outbreaks.
BACKGROUND: A novel oral polio vaccine type 2 (nOPV2), which is more genetically stable (ie, lower risks of reverting to neurovirulence) than the Sabin monovalent OPV2 (mOPV2), has been deployed to interrupt circulating vaccine-derived poliovirus type 2 (PV2) outbreaks. This study compares intestinal mucosal immune responses induced by nOPV2 and mOPV2. METHODS: In this analysis, we evaluated intestinal mucosal immune responses in healthy participants of different ages (ie, infants aged 18-22 weeks, children aged 1-4 years, and adults aged 18-50 years) and vaccine backgrounds (ie, OPV2-experienced vs OPV2-naive). Participants were selected from two phase 2 trials of nOPV2, conducted in 2018-19 (infants and children, NCT03554798 [Panama]; adults, EudraCT 2018-001684-22-NCT04544787 [Belgium]), and two phase 4 historical control trials of mOPV2, conducted in 2015-16 (infants and children, NCT02521974 [Panama]; adults, EudraCT 2015-003325-33 [Belgium]). We measured PV2-specific neutralising activity and IgA concentrations in stools collected before and 14 days after vaccination. FINDINGS: neutralisation titres (1 [IQR 1-1] vs 1 [1-1·5], p=0·89) on day 14, a smaller percentage of OPV2-experienced adults shed vaccine virus than OPV2-naive adults upon nOPV2 challenge (20% vs 82%, p<0·0001). INTERPRETATION: We found no evidence of differences in the intestinal mucosal immune responses induced by nOPV2 or Sabin mOPV2 and observed the strongest responses in infants.
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Godin et al. (2025) studied this question.
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