Key result
Children born after the switch to bivalent oral poliovirus vaccine had significantly lower seroprevalence against PV2 compared to the pre-switch cohort (55.6% vs 93.8%, p<0.0001).
Why the study?
Following the global 2016 switch from trivalent to bivalent oral poliovirus vaccine, poliovirus seroprevalence and factors associated with immunity gaps in Nigeria needed assessment.
Cross-Sectional (n=1,185)
Yes
Absolute Event Rate: 55.6% vs 93.8%
p-value: p=<0.0001
The switch from trivalent to bivalent oral poliovirus vaccine resulted in a significant immunity gap against poliovirus type 2 in Nigerian children born post-switch.
May signal PV2 immunity gaps post-bOPV switch; leaves open optimal surveillance and catch-up strategies.
Introduction: in 2016, a switch from trivalent oral poliovirus vaccine (OPV) (containing serotypes 1,2,3) to bivalent OPV (types 1,3) was implemented globally. We assessed the seroprevalence of poliovirus antibody levels in selected Nigerian states, before and after the switch, documented poliovirus type2 outbreak responses conducted and ascertained factors associated with immunity gaps based on seroprevalence rates. Methods: we conducted a secondary analysis of stored serum samples from the 2018 Nigeria National HIV/AIDS Indicator and Impact Survey. Serum from 1,185 children aged 0-119 months residing in one southern and four northern states were tested for serotype-specific PV neutralizing antibodies; seropositivity was a reciprocal titer ≥8. We conducted regression analysis to determine sociodemographic risk factors associated with low seroprevalence using SAS 9.4. Results: children aged 24-119 months (pre-switch cohort) had seroprevalence against PV1, PV2, and PV3, of 97.3% (95% CI:96.4-98.2), 93.8% (95% CI:92.2-95.5), and 91.3% (95% CI:89.2-93.4), while children aged <24 months (post-switch) had seroprevalence of 86.0% (95% CI:81.2-90.8), 55.6% (95% CI: 47.7-63.4), and 77.2% (95% CI:71.0-83.4) respectively. Regression analysis showed age <24 months was associated with lower seroprevalence against all PV serotypes, (p<0.0001); females had lower seroprevalence against PV1 (p=0.0184) and PV2 (p=0.0354); northern states lower seroprevalence against PV1 (p=0.0039), while well-water source lower seroprevalence against PV3 (p=0.0288). Conclusion: this study showed high seroprevalence rates against PV 1, 2, and 3 in pre-switch children (aged 24-119 months). However, post-switch children (<24 months) had low immunity against PV2 despite outbreak responses. Strategies to increase routine immunization coverage and high-quality polio campaigns can increase immunity against polio virus.
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Bolu et al. (2023) conducted a cross-sectional in Poliovirus immunity (n=1,185). Post-switch cohort (age <24 months) vs. Pre-switch cohort (age 24-119 months) was evaluated on Seroprevalence against PV2 (p=<0.0001). Children born after the switch to bivalent oral poliovirus vaccine had significantly lower seroprevalence against PV2 compared to the pre-switch cohort (55.6% vs 93.8%, p<0.0001).
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