Evidence map›Paper›PMID 35767652›Full record

ArticleScience translational medicine2022

Antibody Fc characteristics and effector functions correlate with protection from symptomatic dengue virus type 3 infection.

Antonio G Dias, Caroline Atyeo, Carolin Loos, Magelda Montoya, Vicky Roy, Sandra Bos, Parnal Narvekar, Tulika Singh, Leah C Katzelnick, Guillermina Kuan and 4 more

Open access · greenAbstract read
In one paragraph

Article in Science translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
11.2field-weighted citation impact, top 1% of its field
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

51 citing papers in PubMed, 60 citations in OpenAlex.

  1. Trial
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  9. Early Fc-effector antibody signatures impact COVID-19 disease trajectory.medRxiv : the preprint server for health sciences · 2026
    Article
  10. Review
  11. Review
  12. Article
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  14. Article
  15. Article
  16. Review
  17. Dengue and severe dengue.Clinical microbiology reviews · 2025
    Review
  18. CD4Vaccines · 2025
    Article
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 2 countries.

Antonio G DiasDivision of Infectious Disease and Vaccinology, School of Public Health, University of California, Berkeley, Berkeley, CA, USA.ORCID 0000-0003-4392-4206
Caroline AtyeoRagon Institute of MGH, MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0002-7489-0232
Carolin LoosRagon Institute of MGH, MIT and Harvard, Cambridge, MA, USA.
Magelda MontoyaDivision of Infectious Disease and Vaccinology, School of Public Health, University of California, Berkeley, Berkeley, CA, USA.
Vicky RoyRagon Institute of MGH, MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0002-5064-1098
Sandra BosDivision of Infectious Disease and Vaccinology, School of Public Health, University of California, Berkeley, Berkeley, CA, USA.ORCID 0000-0001-5036-0336
Parnal NarvekarDivision of Infectious Disease and Vaccinology, School of Public Health, University of California, Berkeley, Berkeley, CA, USA.
Tulika SinghDivision of Infectious Disease and Vaccinology, School of Public Health, University of California, Berkeley, Berkeley, CA, USA.ORCID 0000-0002-7416-7861
Leah C KatzelnickDivision of Infectious Disease and Vaccinology, School of Public Health, University of California, Berkeley, Berkeley, CA, USA.ORCID 0000-0003-1033-6758
Guillermina KuanSustainable Sciences Institute, Managua, Nicaragua.ORCID 0000-0002-5251-173X
Douglas A LauffenburgerMassachusetts Institute of Technology, Cambridge, MA, USA.ORCID 0000-0002-0050-989X
Angel BalmasedaSustainable Sciences Institute, Managua, Nicaragua.
Galit AlterRagon Institute of MGH, MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0002-7680-9215
Eva HarrisDivision of Infectious Disease and Vaccinology, School of Public Health, University of California, Berkeley, Berkeley, CA, USA.ORCID 0000-0002-7238-4037
University of California, Berkeley · USRagon Institute of MGH, MIT and Harvard · USMinisterio de Salud · NIMassachusetts Institute of Technology · USNational Institutes of Health · US

Funding

T Cell Responses Following DENV Natural Infections and Live-Attenuated Dengue Virus VaccinationP01AI106695 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI Eva Harris · 2015 to 2026
$34.1M
Technology CoreU19AI135995 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI Kristian Graugaard Andersen · 2018 to 2026
$32.0M
Immunology, virology, and epidemiology of flaviviruses and other emerging virusesZIAAI001346 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI KATZELNICK, LEAH · 2021 to 2025
$7.1M
Demystifying the antiviral activity of the IgG3+ antibody responseR37AI080289 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI ALTER, GALIT · 2015 to 2022
$5.8M
Living in the post-Zika world: Impact of interactions between dengue and Zika viruses on diagnostics, antibody dynamics, and correlates of disease riskU01AI153416 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI HARRIS, EVA · 2021 to 2025
$4.9M
NIAID NIH HHS HHSN272201000026CNIAID NIH HHS P01 AI106695NIAID NIH HHS R37 AI080289NIAID NIH HHS U01 AI153416NIAID NIH HHS U19 AI135995
6 · The paper itself

Abstract

Preexisting cross-reactive antibodies have been implicated in both protection and pathogenesis during subsequent infections with different dengue virus (DENV) serotypes (DENV1-4). Nonetheless, humoral immune correlates and mechanisms of protection have remained elusive. Using a systems serology approach to evaluate humoral responses, we profiled plasma collected before inapparent or symptomatic secondary DENV3 infection from our pediatric cohort in Nicaragua. Children protected from symptomatic infections had more anti-envelope (E) and anti-nonstructural protein 1 (NS1) total immunoglobulin G (IgG), IgG4, and greater Fc effector functions than those with symptoms. Fc effector functions were also associated with protection from hemorrhagic manifestations in the pre-symptomatic group. Furthermore, in vitro virological assays using these plasma samples revealed that protection mediated by antibody-dependent complement deposition was associated with both lysis of virions and DENV-infected cells. These data suggest that E- and NS1-specific Fc functions may serve as correlates of protection, which can be potentially applied toward the design and evaluation of dengue vaccines.

Indexed as

CoinfectionDengueDengue VirusAntibodies, ViralChildCross ReactionsHumansImmunoglobulin Fc FragmentsImmunoglobulin GAntibodies, ViralImmunoglobulin Fc FragmentsImmunoglobulin G

Identifiers

PMID35767652
PMCPMC10115655
OpenAlexW4283691906

What OpenQuestion holds

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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.