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Correlation of protection against varicella in a randomized Phase III varicella-containing vaccine efficacy trial in healthy infants

Authors :
Michael Povey
Paul Gillard
Vytautas Usonis
Roman Prymula
Jacek Wysocki
Susanna Esposito
Ouzama Henry
Stéphanie Ravault
Ahsan Habib
Stephane Carryn
Source :
Vaccine, Oxford : Elsevier Ltd, 2021, vol. 39, no. 25, p. 3445-3454
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

Background: Varicella vaccination confers high and long-lasting protection against chickenpox and induces robust immune responses, but an absolute correlate of protection (CoP) against varicella has not been established. This study models the relationship between varicella humoral response and protection against varicella. Methods: This was a post-hoc analysis of data from a Phase IIIb, multicenter, randomized trial (NCT00226499) conducted in ten varicella-endemic European countries. Healthy children aged 12–22 months were randomized 3:3:1 to receive one dose of measles-mumps-rubella and one dose of varicella vaccine (one-dose group) or two doses of measles-mumps-rubella-varicella vaccine (two-dose group) or two doses of measles-mumps-rubella vaccine (control group) six weeks apart. The study remained observer-blind until completion, except in countries with obligatory additional immunizations. The objective was to correlate varicella-specific antibody concentrations with protection against varicella and probability of varicella breakthrough, using Cox proportional hazards and Dunning and accelerated failure time statistical models. The analysis was guided by the Prentice framework to explore a CoP against varicella. Results: The trial included 5803 participants, 5289 in the efficacy (2266: one-dose group, 2279: two-dose group and 744: control group) and 5235 (2248, 2245 and 742 in the same groups) in the immunogenicity cohort. The trial ended in 2016 with a median follow-up time of 9.8 years. Six weeks after vaccination with one- or two-dose varicella-containing vaccine, more than 93.0% of vaccinees were seropositive for varicella-specific antibodies. Estimated vaccine efficacy correlated positively with antibody concentrations. The fourth Prentice CoP criterion was not met, due to predicted positive vaccine efficacy in seronegative participants. Further modelling showed decreased probability of moderate to severe varicella breakthrough with increasing varicella-specific antibody concentrations (ten-year probability

Details

ISSN :
0264410X and 18732518
Volume :
39
Database :
OpenAIRE
Journal :
Vaccine
Accession number :
edsair.doi.dedup.....dc239abcd28f21e346d0d42b26edec00