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

TitlePreliminary Findings From the Dynamics of the Immune Responses to Repeat Influenza Vaccination Exposures (DRIVE I) Study: A Randomized Controlled Trial.
Publication TypeJournal Article
Year of Publication2024
AuthorsCowling BJ, San Wong S-, Santos JJS, Touyon L, Ort JT, Ye N, Kwok NKM, Ho F, Cheng SMS, Ip DKM, Peiris M, Webby RJ, Wilson PC, Valkenburg SA, Tsang JS, Leung NHL, Hensley SE, Cobey S
JournalClin Infect Dis
Volume79
Issue4
Pagination901-909
Date Published2024 Oct 15
ISSN1537-6591
KeywordsAdolescent, Adult, Antibodies, Viral, Female, Humans, Influenza A Virus, H1N1 Subtype, Influenza A Virus, H3N2 Subtype, Influenza B virus, Influenza Vaccines, Influenza, Human, Male, Middle Aged, Vaccination, Vaccine Efficacy, Young Adult
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.

DOI10.1093/cid/ciae380
Custom 1

https://www.ncbi.nlm.nih.gov/pubmed/39041887?dopt=Abstract

Alternate JournalClin Infect Dis
PubMed ID39041887
PubMed Central IDPMC11478574
Grant List / / Research Grants Council of the Hong Kong SAR Government /
/ / National Institute of Allergy and Infectious Diseases /
75N93021C00016 / AI / NIAID NIH HHS / United States
/ / Theme-based Research Scheme /
UL1 TR002384 / TR / NCATS NIH HHS / United States
U01 AI153700 / AI / NIAID NIH HHS / United States
/ NH / NIH HHS / United States
75N93021C00015 / AI / NIAID NIH HHS / United States

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