Preliminary Findings From the Dynamics of the Immune Responses to Repeat Influenza Vaccination Exposures (DRIVE I) Study: A Randomized Controlled Trial

Author:

Cowling Benjamin J12ORCID,Wong Sook-San13,Santos Jefferson J S4,Touyon Lisa13,Ort Jordan T4,Ye Naiqing4,Kwok Natalie K M1,Ho Faith1,Cheng Samuel M S1,Ip Dennis K M1,Peiris Malik1,Webby Richard J5,Wilson Patrick C6,Valkenburg Sophie A37,Tsang John S8,Leung Nancy H L12,Hensley Scott E4,Cobey Sarah9

Affiliation:

1. WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong , Hong Kong Special Administrative Region , China

2. Laboratory of Data Discovery for Health Limited, Hong Kong Science and Technology Park , New Territories, Hong Kong Special Administrative Region , China

3. HKU-Pasteur Research Pole, Li Ka Shing Faculty of Medicine, The University of Hong Kong , Hong Kong Special Administrative Region , China

4. Department of Microbiology, Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania , USA

5. Department of Infectious Diseases, St Jude Children's Research Hospital , Memphis, Tennessee , USA

6. Gale and Ira Drukier Institute for Children's Health, Weill Cornell Medicine , New York, New York , USA

7. Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne , Melbourne, Victoria , Australia

8. Yale Center for Systems and Engineering Immunology and Department of Immunobiology, Yale University School of Medicine , New Haven, Connecticut , USA

9. Department of Ecology and Evolution, University of Chicago , Chicago, Illinois , USA

Abstract

Abstract Background Studies have reported that repeated annual vaccination may influence influenza vaccination effectiveness in the current season. Methods We established a 5-year randomized placebo-controlled trial of repeated influenza vaccination (Flublok; Sanofi Pasteur) in adults 18–45 years of age. In the first 2 years, participants were randomized to receive vaccine or saline placebo as follows: placebo-placebo (P-P), placebo-vaccine (P-V), or vaccine-vaccine (V-V). Serum samples were collected each year just before vaccination and after 30 and 182 days. A subset of serum samples collected at 5 time points from 95 participants were tested for antibodies against vaccine strains. Results From 23 October 2020 through 11 March 2021 we enrolled and randomized 447 adults. Among vaccinated individuals, antibody titers increased between days 0 and 30 against each of the vaccine strains, with smaller increases for repeat vaccinees who on average had higher prevaccination titers in year 2. There were statistically significant differences in the proportions of participants achieving ≥4-fold rises in antibody titer for the repeat vaccinees for influenza A(H1N1), B/Victoria, and B/Yamagata, but not for A(H3N2). Among participants who received vaccination in year 2, there were no significant differences between the P-V and V-V groups in geometric mean titers at day 30 or the proportions of participants with antibody titers ≥40 at day 30 for any of the vaccine strains. Conclusions In the first 2 years, during which influenza did not circulate, repeat and first-time vaccinees had similar postvaccination geometric mean titers to all 4 vaccine strains, indicative of similar levels of clinical protection. Clinical Trials Registration. NCT04576377

Publisher

Oxford University Press (OUP)

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