Evidence map›Paper›PMID 41479919›Full record

ArticleFrontiers in immunology2025

COVID-19 vaccination induces cross-reactive dengue virus antibodies with altered isotype profiles and

Sebastian Reinig, Chin Kuo, Sheng-Yu Huang, Kuei-Ching Hsiung, Po-Kai Chen, Etsuro Ito, Ing-Kit Lee, Ching-Yen Tsai, Shu-Min Lin, Shin-Ru Shih

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Sebastian ReinigResearch Center for Emerging Viral Infections, Chang Gung University, Taoyuan, Taiwan.
Chin KuoResearch Center for Emerging Viral Infections, Chang Gung University, Taoyuan, Taiwan.
Sheng-Yu HuangResearch Center for Emerging Viral Infections, Chang Gung University, Taoyuan, Taiwan.
Kuei-Ching HsiungResearch Center for Emerging Viral Infections, Chang Gung University, Taoyuan, Taiwan.
Po-Kai ChenDepartment of Biology, Waseda University, Tokyo, Japan.
Etsuro ItoDepartment of Biology, Waseda University, Tokyo, Japan.
Ing-Kit LeeDivision of Infectious Diseases, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
Ching-Yen TsaiDivision of Infectious Disease, Department of Internal Medicine, Kaohsiung Municipal Feng-Shan Hospital, Kaohsiung, Taiwan.
Shu-Min LinDepartment of Thoracic Medicine, Chang Gung Memorial Hospital, Chang Gung University, School of Medicine, Taoyuan, Taiwan.
Shin-Ru ShihResearch Center for Emerging Viral Infections, Chang Gung University, Taoyuan, Taiwan.

Funding

University of Washington Arboviral Research Network (UWARN)U01AI151698 · NIAID · UNIVERSITY OF WASHINGTON · PI Michael Gale, PETER MACGARR RABINOWITZ · 2020 to 2026
$13.3M
NIAID NIH HHS U01 AI151698
6 · The paper itself

Abstract

Background: SARS-CoV-2 infection and COVID-19 vaccination can induce antibodies that cross-react with dengue virus (DENV). Pre-existing IgG antibodies against DENV are known to enhance infection through antibody-dependent enhancement (ADE) via Fcγ receptors. COVID-19 vaccines induce an altered IgG subclass distribution with modified Fcγ receptor affinity. This study investigates the isotype profile of DENV cross-reactive antibodies induced by COVID-19 vaccination and their potential to mediate ADE. Methods: We retrospectively collected 271 serum samples from individuals in Taiwan who were either SARS-CoV-2-unvaccinated, vaccinated with 1-3 doses of COVID-19 vaccine, recipients of an Omicron-era booster, or previously recovered from dengue infection. Antibody titers (IgM, IgA, and IgG subclasses 1-4) against SARS-CoV-2 spike (S) glycoprotein and DENV serotype 2 envelope (E) protein were measured by enzyme-linked immunosorbent assay (ELISA). Selective depletion of anti-S or anti-E antibodies was performed to confirm cross-reactivity. ADE activity was assessed Results: Cross-reactive anti-E antibodies in COVID-19-vaccinated individuals were predominantly IgM and IgA, whereas anti-S antibodies in vaccinated individuals and anti-E antibodies in dengue-recovered patients were dominated by IgG1. Low levels of cross-reactive anti-E IgG detected in vaccinated individuals were mainly of the low-affinity IgG2 and IgG4 subclasses. These vaccine-induced cross-reactive antibodies mediated significantly stronger Conclusion: COVID-19 vaccination induces DENV cross-reactive antibodies with a distinct isotype profile and distinct ADE compared with natural dengue infection. Due to low Fc-affinity these antibodies likely do not pose a threat of dengue. These findings highlight the importance of considering off-target immunity and ADE risk in future vaccine design.

Indexed as

Antibodies, ViralAntibody-Dependent EnhancementCOVID-19COVID-19 VaccinesDengueDengue VirusImmunoglobulin IsotypesSARS-CoV-2AdultAgedCross ReactionsFemaleHumansImmunoglobulin GMaleMiddle AgedAntibodies, ViralCOVID-19 VaccinesImmunoglobulin GImmunoglobulin IsotypesReceptors, IgGSpike Glycoprotein, Coronavirusantibody-dependent enhancementCOVID-19cross-reactivedengueisotype

Identifiers

PMID41479919
PMCPMC12753992

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.