Key result
IPV shows comparable pharyngeal shedding to bOPV after nOPV2 challenge despite higher neutralizing antibodies.
Why the study?
The impact of prior inactivated poliovirus vaccine (IPV) doses on nasal and pharyngeal viral replication following subsequent poliovirus exposure remains unclear.
Does inactivated poliovirus vaccine reduce pharyngeal shedding and improve mucosal immunity following nOPV2 challenge in polio vaccine-naïve infants compared to bOPV?
RCT (n=500)
Open-label
1:1 ratio
Yes
Does inactivated poliovirus vaccine reduce pharyngeal shedding and improve mucosal immunity following nOPV2 challenge in polio vaccine-naïve infants compared to bOPV?
Relative Risk: 0.65 (95% CI 0.2–2.13)
Absolute Event Rate: 1.7% vs 2.6%
IPV induces strong nasal and serum immunity and limits pharyngeal shedding upon nOPV2 challenge, supporting its potential role in outbreak response in IPV-only settings.
Supports IPV for nOPV2 outbreak response in IPV-only settings; confirms comparable shedding control with superior nasal and serum immunity.
BACKGROUND: Impact of prior inactivated poliovirus vaccine (IPV) doses on nasal and pharyngeal viral replication following subsequent poliovirus exposure remains unclear. Circulating vaccine-derived poliovirus detection in IPV-only countries necessitates better understanding of IPV's role in inducing nasal and pharyngeal mucosal immunity. METHODS: This multicenter, randomized, open-label, parallel-group trial (9 November 2023-25 August 2024; ClinicalTrials.gov identifier: NCT05677256) was conducted in Bangladesh in 500 polio vaccine-naïve infants aged 6-8 weeks. Two infant cohorts (vaccinated with 3 doses of either IPV or bivalent oral poliovirus vaccine [bOPV]) were challenged at 18-20 weeks with novel OPV type 2 (nOPV2). Pharyngeal and fecal viral shedding, and nasal, intestinal, and serum immune responses were measured post-nOPV2-challenge. RESULTS: Poliovirus type 2 (PV2) pharyngeal shedding was minimal post-challenge (1.7% of IPV-vaccinated and 2.6% of bOPV-vaccinated infants). Nasal PV2-specific neutralizing antibody titers were higher in the IPV group post-nOPV2-challenge (day 14; geometric mean titers [GMT]: IPV, 7.5 [95% CI: 5.1-11.1] vs bOPV, 0.6 [95% CI: 0.3-1.2]). Stool PV2-specific neutralization titers were comparable at day 14 (GMT: IPV, 124.0 [95% CI: 54.7-281.0] vs bOPV, 127.3 [95% CI: 74.0-218.9]). Serum PV2 neutralizing antibody titers were consistently higher in IPV group, peaking at day 28 (GMT: IPV, 4347.4 [95% CI: 2378.2-7947.2] vs bOPV, 259.9 [95% CI: 115.5-584.9]). CONCLUSIONS: nOPV2 pharyngeal shedding was low following IPV or bOPV vaccination, whereas IPV induced higher nasal and serum, and comparable intestinal PV2-specific immunity, suggesting a potential role for IPV in poliovirus outbreak response in IPV-only settings.
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Zaman et al. (2026) conducted an RCT in Polio vaccine-naïve infants (n=500). Inactivated poliovirus vaccine (IPV) vs. Bivalent oral poliovirus vaccine (bOPV) was evaluated on Pharyngeal shedding of vaccine virus (ever detectable PV2 RT-PCR 0-28 days post-challenge) (RR 0.65, 95% CI 0.20-2.13). Inactivated poliovirus vaccine resulted in minimal pharyngeal shedding (1.7%) comparable to bOPV (2.6%) following nOPV2 challenge, while inducing higher nasal and serum neutralizing antibodies.
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