Abstract

BackgroundThere is a demand of affordable IPV in the World. Statens Serum Institut (SSI) has developed three reduced dose IPV formulations adsorbed to aluminium hydroxide; 1/3 IPV-Al, 1/5 IPV-Al and 1/10 IPV-Al SSI, and now report the results of the first investigations in humans. Methods240 Danish adolescents, aged 10–15years, and childhood vaccinated with IPV were booster vaccinated with 1/3 IPV-Al, 1/5 IPV-Al, 1/10 IPV-Al or IPV Vaccine SSI. The booster effects (GMTRs) of the three IPV-Al SSI were compared to IPV Vaccine SSI, and evaluated for non-inferiority. Immunogenicity resultsThe pre-vaccination GMTs were similar across the groups; 926 (type 1), 969 (type 2) and 846 (type 3) in the total trial population.The GMTRs by poliovirus type and IPV formulation were:Type 1: 17.0 (1/3 IPV-Al), 13.0 (1/5 IPV-Al), 7.1 (1/10 IPV-Al) and 42.2 (IPV Vaccine SSI).Type 2: 12.5 (1/3 IPV-Al), 13.1 (1/5 IPV-Al), 7.6 (1/10 IPV-Al) and 47.8 (IPV Vaccine SSI).Type 3: 14.5 (1/3 IPV-Al), 16.2 (1/5 IPV-Al), 8.9 (1/10 IPV-Al) and 62.4 (IPV Vaccine SSI)Thus, the three IPV-Al formulations were highly immunogenic, but inferior to IPV Vaccine SSI, in this booster vaccination trial. Safety resultsNo SAE and no AE of severe intensity occurred. 59.2% of the subjects reported at least one AE. Injection site pain was the most frequent AE in all groups; from 24.6% to 43.3%. Injection site redness and swelling frequencies were<5% in most and<10% in all groups. The most frequent systemic AEs were fatigue (from 8.2% to 15.0%) and headache (from 15.0% to 28.3%). Most AEs were of mild intensity. In conclusion, the three IPV-Al SSI were safe in adolescents and the booster effects were satisfactory.ClinicalTrials.gov registration number: NCT02280447.

Highlights

  • The World Health Assembly launched the global polio eradication initiative (GPEI) in 1988, and as per the most recent strategic plan from 2012 [1], the last case of paralytic polio caused by wild poliovirus is expected to occur in the near future

  • The first step is introduction of bivalent oral polio vaccine (OPV) which contains poliovirus types 1 and 3 only, and cessation of the use of trivalent OPV, a process that is presently ongoing in the concerned countries. bOPV will accelerate circulating vaccinederived poliovirus (cVDPV) elimination, as most cVDPVs are type 2 [2,3]

  • Statens Serum Institut (SSI) has developed three reduced dose inactivated polio vaccine (IPV) formulations by adsorption of the inactivated virus to aluminium hydroxide adjuvant, named; 1/3 IPV-Al SSI, 1/5 IPV-Al SSI and 1/10 IPV-Al SSI, and we report the results of the first investigations of these vaccines in humans

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Summary

Introduction

The World Health Assembly launched the global polio eradication initiative (GPEI) in 1988, and as per the most recent strategic plan from 2012 [1], the last case of paralytic polio caused by wild poliovirus is expected to occur in the near future. Part of the GPEI is cessation of the use of oral polio vaccine (OPV) due to the risks of. The fact that bOPV does not protect against type 2 poliovirus is partly justified by the last wild type 2 polio case dating back to 1999, and a historically low risk of cVDPV2, as a result of GPEI activities [4,5,6,7]. The GMTRs by poliovirus type and IPV formulation were: Type 1: 17.0 (1/3 IPV-Al), 13.0 (1/5 IPV-Al), 7.1 (1/10 IPV-Al) and 42.2 (IPV Vaccine SSI). Type 3: 14.5 (1/3 IPV-Al), 16.2 (1/5 IPV-Al), 8.9 (1/10 IPV-Al) and 62.4

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