Immuno-persistence of the different primary polio vaccine schedules and immunogenicity of the booster dose by sabin inactivated or bivalent oral poliovirus vaccine in children aged 4 years: an open-label, randomised, controlled phase 4 trial in China

Xuewen Tang; Yanhui Xiao; Xuan Deng; Yang Zhou; Haiping Chen; Rui Yan; Yao Zhu; Shengyi Wang; Hui Wang; Xiujuan Zhu; Linyun Luo; Yan Liu; Zhiying Yin; Guoping Zhang; Zhongbing Chen; Jian Jiang; Xiaoming Yang; Hanqing He

doi:10.1016/j.lanwpc.2023.100725

Immuno-persistence of the different primary polio vaccine schedules and immunogenicity of the booster dose by sabin inactivated or bivalent oral poliovirus vaccine in children aged 4 years: an open-label, randomised, controlled phase 4 trial in China

Lancet Reg Health West Pac. 2023 Mar 17:34:100725. doi: 10.1016/j.lanwpc.2023.100725. eCollection 2023 May.

Authors

Xuewen Tang¹, Yanhui Xiao², Xuan Deng¹, Yang Zhou¹, Haiping Chen², Rui Yan¹, Yao Zhu¹, Shengyi Wang², Hui Wang³, Xiujuan Zhu³, Linyun Luo², Yan Liu⁴, Zhiying Yin⁵, Guoping Zhang⁶, Zhongbing Chen⁷, Jian Jiang⁶, Xiaoming Yang², Hanqing He¹

Affiliations

¹ Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou, Zhejiang, China.
² China National Biotec Group Company Limited, Beijing, China.
³ Beijing Institute of Biological Products Company Limited, Beijing, China.
⁴ Hangzhou Municipal Center for Disease Control and Prevention, Hangzhou, Zhejiang, China.
⁵ Quzhou Municipal Center for Disease Control and Prevention, Quzhou, Zhejiang, China.
⁶ Chun'an County Center for Disease Control and Prevention, Hangzhou, Zhejiang, China.
⁷ Longyou County Center for Disease Control and Prevention, Hangzhou, Zhejiang, China.

Abstract

Background: Sabin inactivated and bivalent oral poliovirus vaccine (sIPV, bOPV) were commonly used in China since 2016. We conducted an open-label, randomised, controlled phase 4 trial to assess immune persistence following sequential immunisation with sIPV or bOPV, and immunogenicity and safety of a booster dose of poliovirus vaccine in children aged 4 years.

Methods: Participants from a previous clinical trial with three different sequential schedules with sIPV (I) or bOPV (B) at ages 2, 3, and 4 months (Groups I-B-B, I-I-B, I-I-I) in 2017 were followed-up. The children were further divided into five subgroups after sIPV was given for Group I-B-B, and sIPV or bOPV randomly given for Group I-I-B and Group I-I-I (128 children in Groups I-B-B-I, 60 in Group I-I-B-B, 64 in Group I-I-B-I, 68 in Group I-I-I-B, 67 in Group I-I-I-I). Immune persistence and immunogenicity were assessed by measuring poliovirus type-specific antibodies, and safety were analysed in all children who received the booster dose.

Findings: Between Dec 5, 2020 and Jun 30, 2021, we respectively enrolled 381 participants in the immune persistence analysis, and 352 participants in per protocol (PP) analysis of the immunogenicity of the booster immunisation. Seropositivity rates of antibodies against poliovirus types 1 and 3 were all >90% four years after primary immunisation, while for poliovirus type 2 were 46.83%, 75.41%, and 90.23% (χ² = 60.948, P < 0.001) for Groups I-B-B, I-I-B, and I-I-I, respectively. After the booster dose, seropositivity rates were 100% for all three serotypes in Group I-B-B-I, I-I-B-I and I-I-I-I; In Group I-I-B-B and I-I-I-B, the seropositivity rates for types 1 and 3 were all 100%, for type 2 were 92.59% and 98.46%. The geometric mean titres (GMTs) against poliovirus 1 and 3 were all high in five groups (>1860.73), and the GMTs against type 2 were significantly lower in groups booster with bOPV: Group I-I-B-B (50.60) and Group I-I-I-B (247.84). There was no significant difference in seropositivity rates or GMTs for all three serotypes (P > 0.05) between Group I-I-B-I and I-I-I-I. No serious adverse events occurred during the study.

Interpretation: Our findings suggest that at least two sIPV doses are needed in the current routine poliovirus immunisation schedule, and schedules containing 3 or 4 doses of sIPV provide better protection against poliovirus type 2 than the current sIPV-sIPV-bOPV-bOPV schedule in China.

Funding: Medical and Health Science and Technology of Zhejiang Province (2021KY118). This trial was registered with ClinicalTrials.gov (NCT04576910).

Keywords: Booster dose; Immunogenicity; Persistence immunity; Poliovirus; Sabin strain.

Associated data

ClinicalTrials.gov/NCT04576910