Evidence map›Paper›PMID 32760128›Full record

ArticlePLoS pathogens2020

A cross-reactive antibody protects against Ross River virus musculoskeletal disease despite rapid neutralization escape in mice.

Julie M Fox, Ling Huang, Stephen Tahan, Laura A Powell, James E Crowe, David Wang, Michael S Diamond

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  12. Ly6CCell reports · 2024
    Article
  13. Mayaro virus pathogenesis and immunity in rhesus macaques.PLoS neglected tropical diseases · 2023
    Article
  14. Article
  15. Article
  16. Review
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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

7 authors at 3 institutions in 1 country.

Julie M FoxDepartment of Medicine, Washington University in St. Louis, St. Louis, Missouri, United States of America.ORCID 0000-0003-0567-738X
Ling HuangMacroGenics, Rockville, Maryland, United States of America.
Stephen TahanDepartment of Molecular Microbiology, Washington University in St. Louis, St. Louis, Missouri, United States of America.ORCID 0000-0002-5895-8698
Laura A PowellDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.ORCID 0000-0002-8227-697X
James E CroweDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.ORCID 0000-0002-0049-1079
David WangDepartment of Molecular Microbiology, Washington University in St. Louis, St. Louis, Missouri, United States of America.
Michael S DiamondDepartment of Medicine, Washington University in St. Louis, St. Louis, Missouri, United States of America.ORCID 0000-0002-8791-3165
Washington University in St. Louis · USVanderbilt University Medical Center · USMacroGenics (United States) · US

Funding

Specific and Broadly Active Monoclonal Antibody Therapeutics Against The FilovirusesU19AI142790 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI SAPHIRE, ERICA OLLMANN · 2019 to 2023
$40.0M
Structural and functional basis of ultra potent CHKV neutralization by human mAbsR01AI114816 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CROWE, JAMES E, DIAMOND, MICHAEL S · 2015 to 2019
$3.7M
MOLECULAR PARASITOLOGY TRAINING PROGRAMT32AI007281 · NIAID · MEHARRY MEDICAL COLLEGE · PI NDE, PIUS N · 1985 to 2025
$3.2M
Impairment of B cell Responses by Pathogenic Chikungunya VirusesR01AI141436 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DIAMOND, MICHAEL S, MORRISON, THOMAS E · 2019 to 2023
$3.2M
IFN Dependent Control of Acute and Chronic Chikungunya Virus Induced DiseaseR01AI127513 · NIAID · WASHINGTON UNIVERSITY · PI DIAMOND, MICHAEL S, LENSCHOW, DEBORAH J · 2017 to 2020
$2.1M
NIAID NIH HHS HHSN272201400018CNIAID NIH HHS R01 AI114816NIAID NIH HHS R01 AI127513NIAID NIH HHS R01 AI141436NIAID NIH HHS T32 AI007281NIAID NIH HHS U19 AI142790
6 · The paper itself

Abstract

Arthritogenic alphaviruses cause debilitating musculoskeletal disease and historically have circulated in distinct regions. With the global spread of chikungunya virus (CHIKV), there now is more geographic overlap, which could result in heterologous immunity affecting natural infection or vaccination. Here, we evaluated the capacity of a cross-reactive anti-CHIKV monoclonal antibody (CHK-265) to protect against disease caused by the distantly related alphavirus, Ross River virus (RRV). Although CHK-265 only moderately neutralizes RRV infection in cell culture, it limited clinical disease in mice independently of Fc effector function activity. Despite this protective phenotype, RRV escaped from CHK-265 neutralization in vivo, with resistant variants retaining pathogenic potential. Near the inoculation site, CHK-265 reduced viral burden in a type I interferon signaling-dependent manner and limited immune cell infiltration into musculoskeletal tissue. In a parallel set of experiments, purified human CHIKV immune IgG also weakly neutralized RRV, yet when transferred to mice, resulted in improved clinical outcome during RRV infection despite the emergence of resistant viruses. Overall, this study suggests that weakly cross-neutralizing antibodies can protect against heterologous alphavirus disease, even if neutralization escape occurs, through an early viral control program that tempers inflammation.

Indexed as

Alphavirus InfectionsAnimalsAntibodies, NeutralizingAntibodies, ViralCross ReactionsFemaleMaleMiceMice, Inbred C57BLMusculoskeletal DiseasesReceptors, FcRoss River virusViral LoadVirulenceAntibodies, NeutralizingAntibodies, ViralReceptors, Fc

Identifiers

PMID32760128
PMCPMC7433899
OpenAlexW3047352002

What OpenQuestion holds

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LicenceCC BY
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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.