Evidence map›Paper›PMID 36402135›Full record

ArticleCell2022

A Zika virus-specific IgM elicited in pregnancy exhibits ultrapotent neutralization.

Tulika Singh, Kwan-Ki Hwang, Andrew S Miller, Rebecca L Jones, Cesar A Lopez, Sarah J Dulson, Camila Giuberti, Morgan A Gladden, Itzayana Miller, Helen S Webster and 19 more

Open access · greenAbstract read
In one paragraph

Article in Cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

32 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
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  11. Dengue and severe dengue.Clinical microbiology reviews · 2025
    Review
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  15. Article
  16. Article
  17. Zika virus: an overview update.Current opinion in HIV and AIDS · 2025
    Review
  18. Review
  19. Evolution of Zika virus inVirus evolution · 2025
    Article
  20. Immunoglobulin M response in largemouth bass (Frontiers in immunology · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors at 8 institutions in 5 countries.

Tulika SinghDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA; Division of Infectious Diseases and Vaccinology, School of Public Health, University of California, Berkeley, Berkeley, CA 94709, USA.
Kwan-Ki HwangDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
Andrew S MillerDepartment of Biological Sciences, Purdue Institute of Inflammation, Immunology, and Infectious Disease, Purdue University, West Lafayette, IN 47907, USA.
Rebecca L JonesDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
Cesar A LopezDepartment of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Sarah J DulsonDepartment of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Camila GiubertiNúcleo de Doenças Infecciosas-Universidade Federal do Espίrito Santo, Vitoria, Espίrito Santo 29075-910, Brazil.
Morgan A GladdenDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
Itzayana MillerDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA; Department of Pediatrics, Weill Cornell Medicine, New York City, NY 10065, USA.
Helen S WebsterDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
Joshua A EudaileyDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA; Department of Pediatrics, Weill Cornell Medicine, New York City, NY 10065, USA.
Kan LuoDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
Tarra Von HolleDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
Robert J EdwardsDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
Sarah ValenciaDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
Katherine E BurgomasterViral Pathogenesis Section, Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892 USA.
Summer ZhangDuke-National University of Singapore Medical School, 169857, Singapore.
Jesse F MangoldDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
Joshua J TuDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
Maria DennisDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
S Munir AlamDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710, USA.
Lakshmanane PremkumarDepartment of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Reynaldo DietzeNúcleo de Doenças Infecciosas-Universidade Federal do Espίrito Santo, Vitoria, Espίrito Santo 29075-910, Brazil; Global Health & Tropical Medicine, Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, Lisbon 1349-008, Portugal.
Theodore C PiersonViral Pathogenesis Section, Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892 USA.
Eng Eong OoiDuke-National University of Singapore Medical School, 169857, Singapore.
Helen M LazearDepartment of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Richard J KuhnDepartment of Biological Sciences, Purdue Institute of Inflammation, Immunology, and Infectious Disease, Purdue University, West Lafayette, IN 47907, USA.
Sallie R PermarDepartment of Pediatrics, Weill Cornell Medicine, New York City, NY 10065, USA. Electronic address: sap4017@med.cornell.edu.
Mattia BonsignoriTranslational Immunobiology Unit, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: mattia.bonsignori@nih.gov.
Duke University · USUniversity of North Carolina at Chapel Hill · USNational Institutes of Health · USNational University of Singapore · SGPurdue University West Lafayette · USCornell University · USInstituto de Medicina Tropical · PYUniversidade Federal do Espírito Santo · BR

Funding

SEEDING POSTDOCTORAL INNOVATORS IN RESEARCH &EDUCATIONK12GM000678 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DONALD T LYSLE, Kathryn Joanna Reissner · 1999 to 2026
$30.9M
Antibody-based Protection against FlavivirsesR01AI073755 · NIAID · WASHINGTON UNIVERSITY · PI DIAMOND, MICHAEL S, FREMONT, DAVED H. · 2007 to 2022
$11.4M
Protective Immune Mechanisms against Zika Virus Infection in the Female Reproductive TractR21AI144631 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LAZEAR, HELEN · 2019 to 2020
$422k
The relationship between maternal ZIKV-specific and ADE antibodies and fetal outcomeR21AI132677 · NIAID · DUKE UNIVERSITY · PI SWAMY, GEETA K. · 2018 to 2019
$399k
The Role of Dengue Virus Antibodies in Vector-independent transmission of Zika VirusF31AI143237 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LOPEZ, CESAR AUGUSTO · 2019 to 2022
$158k
NIAID NIH HHS F31 AI143237NIAID NIH HHS HHSN272201700060CNIAID NIH HHS R01 AI073755NIAID NIH HHS R21 AI132677NIAID NIH HHS R21 AI144631NIGMS NIH HHS K12 GM000678
6 · The paper itself

Abstract

Congenital Zika virus (ZIKV) infection results in neurodevelopmental deficits in up to 14% of infants born to ZIKV-infected mothers. Neutralizing antibodies are a critical component of protective immunity. Here, we demonstrate that plasma IgM contributes to ZIKV immunity in pregnancy, mediating neutralization up to 3 months post-symptoms. From a ZIKV-infected pregnant woman, we isolated a pentameric ZIKV-specific IgM (DH1017.IgM) that exhibited ultrapotent ZIKV neutralization dependent on the IgM isotype. DH1017.IgM targets an envelope dimer epitope within domain II. The epitope arrangement on the virion is compatible with concurrent engagement of all ten antigen-binding sites of DH1017.IgM, a solution not available to IgG. DH1017.IgM protected mice against viremia upon lethal ZIKV challenge more efficiently than when expressed as an IgG. Our findings identify a role for antibodies of the IgM isotype in protection against ZIKV and posit DH1017.IgM as a safe and effective candidate immunotherapeutic, particularly during pregnancy.

Indexed as

Immunoglobulin MPregnancyZika VirusZika Virus InfectionAnimalsAntibodies, NeutralizingAntibodies, ViralEpitopesFemaleMiceNeutralization TestsAntibodies, NeutralizingAntibodies, ViralEpitopesImmunoglobulin Mcross-linkingIgMimmunotherapyisotypemultivalent bindingneutralizationpregnancytherapeutic antibodiesZika

Identifiers

PMID36402135
PMCPMC9742325
OpenAlexW4309438501

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Registered trials

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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.