Evidence map›Paper›PMID 40946064›Full record

ArticleVaccine2025

High-resolution antibody dynamics following influenza vaccination reveal predominantly weak responses as well as infrequent but durable immunity across the 2014-2022 seasons.

Aaron Lane, Huy Q Quach, Inna G Ovsyannikova, Richard B Kennedy, Ted M Ross, Tal Einav

Abstract read
In one paragraph

Article in Vaccine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Aaron LaneCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, CA 92037, USA.
Huy Q QuachVaccine Research Group, Mayo Clinic, Rochester, MN 55905, USA.
Inna G OvsyannikovaVaccine Research Group, Mayo Clinic, Rochester, MN 55905, USA.
Richard B KennedyVaccine Research Group, Mayo Clinic, Rochester, MN 55905, USA.
Ted M RossCenter for Vaccines and Immunology, University of Georgia, Athens, GA 30602, USA; Department of Infectious Diseases, University of Georgia, Athens, GA 30602, USA; Florida Research and Innovation Center, Cleveland Clinic, Port Saint Lucie, FL 34987, USA; Department of Infection Biology, Lehner Research Institute, Cleveland Clinic, Cleveland, OH 44106, USA.
Tal EinavCenter for Vaccine Innovation, La Jolla Institute for Immunology, La Jolla, CA 92037, USA; Department of Medicine, University of California San Diego, La Jolla, CA 92037, USA. Electronic address: tal.einav@lji.org.

Funding

Implementing a Maternal health and PRegnancy Outcomes Vision for Everyone (IMPROVE)UL1TR002378 · NCATS · EMORY UNIVERSITY · PI Andres J Garcia, Elizabeth O. Ofili · 2017 to 2026
$92.1M
COVID Supplement - COMPONENT A OF THE COLLABORATIVE INFLUENZA VACCINE INNOVATION CENTERS (CIVICS) PROGRAM TO DESIGN AND EVALUATE INNOVATIVE INFLUENZA VACCINE APPROACHES,75N93019C00052 · NIAID · UNIVERSITY OF GEORGIA · PI ROSS, TED · 2019 to 2025
$74.6M
NCATS NIH HHS UL1 TR002378NIAID NIH HHS 75N93019C00052NIH HHS 75N93019C00052
6 · The paper itself

Abstract

Most influenza vaccine studies evaluate acute antibody responses 1 month post-vaccination, yet the finer details of immune kinetics remain poorly understood. Here, we conducted two new vaccine studies and analyzed 12 prior vaccine studies to map antibody responses against H3N2 and H1N1 influenza in high resolution from the day of vaccine administration out to 1 year post-vaccination. Antibody kinetics corresponded to three major phenotypes, namely, weak (<4x fold-change at 1 month and 1 year), transient (≥4x at 1 month, <4x at 1 year), or durable (≥4x at 1 month and 1 year). Surprisingly, ≥50 % of vaccine recipients were weak across nearly all seasons, age groups, sexes, pre-vaccination titers, and high or standard vaccine doses examined. Peak fold-change at 1 month post-vaccination was strongly associated with the long-term response, with transient responders often achieving a peak fold-change of 4x and then decaying back to baseline, while durable responders reached ≥16x fold-change and maintained comparable titers out to 1 year. Using the weak, transient, and durable trajectories, a single time point early in the response (days 7-8 or 21) predicted an individual's response out to 1 year post-vaccination. These results highlight the stark heterogeneity that is consistently seen across influenza seasons, where the vaccine elicits little-to-no response in some but strong and long-lasting antibody immunity in others.

Indexed as

Antibodies, ViralInfluenza, HumanInfluenza VaccinesAdolescentAdultAgedAntibody FormationChildChild, PreschoolFemaleHumansInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeMaleMiddle AgedSeasonsAntibodies, ViralInfluenza VaccinesAntibody responseHemagglutination inhibitionInfluenzaPredictive modelingTime dynamicsVaccinationVaccine durabilityVaccine waning

Identifiers

PMID40946064
PMCPMC12435915

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.