Evidence map›Paper›PMID 33326804›Full record

ArticleThe Journal of allergy and clinical immunology2021

Suppression of IgE-mediated anaphylaxis and food allergy with monovalent anti-FcεRIα mAbs.

Marat V Khodoun, Suzanne C Morris, Wen-Hai Shao, Crystal Potter, Elizabeth Angerman, Artem Kiselev, Alexander E Yarawsky, Andrew B Herr, Katja Klausz, Anna Otte and 2 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Traditional Chinese Medicine for Pediatric Allergic Diseases.Current allergy and asthma reports · 2025
    Review
  5. Importance of mast cell histamine secretion in IgG-mediated systemic anaphylaxis.The Journal of allergy and clinical immunology · 2025
    Article
  6. Review
  7. Review
  8. Article
  9. Optimizing drug inhibition of IgE-mediated anaphylaxis in mice.The Journal of allergy and clinical immunology · 2022
    Article
  10. Licochalcone A inhibits IgE-mediated allergic reaction through PLC/ERK/STAT3 pathway.International journal of immunopathology and pharmacology
    Article
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

12 authors at 5 institutions in 3 countries.

Marat V KhodounDivision of Allergy, Immunology and Rheumatology, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Suzanne C MorrisDivision of Allergy, Immunology and Rheumatology, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Wen-Hai ShaoDivision of Allergy, Immunology and Rheumatology, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Crystal PotterDivision of Allergy, Immunology and Rheumatology, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Elizabeth AngermanDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Artem KiselevInstitute of Cytology, Russian Academy of Sciences, Saint Petersburg, Russia.
Alexander E YarawskyDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Andrew B HerrDivision of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio; Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Katja KlauszDivision of Stem Cell Transplantation and Immunotherapy, University Hospital Schleswig-Holstein, University of Kiel, Kiel, Germany.
Anna OtteDivision of Stem Cell Transplantation and Immunotherapy, University Hospital Schleswig-Holstein, University of Kiel, Kiel, Germany.
Matthias PeippDivision of Stem Cell Transplantation and Immunotherapy, University Hospital Schleswig-Holstein, University of Kiel, Kiel, Germany.
Fred D FinkelmanDivision of Allergy, Immunology and Rheumatology, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio; Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio. Electronic address: finkelfd@ucmail.uc.edu.
Cincinnati Children's Hospital Medical Center · USUniversity of Cincinnati Medical Center · USUniversity Hospital Schleswig-Holstein · DEInstitute of Cytology · RUUniversity of Lübeck · DE

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Alexander Miethke · 2007 to 2026
$24.4M
Rapid, safe suppression of IgE-mediated disease with monovalent anti-ceRIa mAbR01AI145991 · NIAID · UNIVERSITY OF CINCINNATI · PI FINKELMAN, FRED DOUGLASS, KHODOUN, MARAT · 2019 to 2023
$2.6M
Wimpy antibody isotypes protect against antibody-mediated diseaseR01AI130103 · NIAID · UNIVERSITY OF CINCINNATI · PI FINKELMAN, FRED DOUGLASS · 2017 to 2021
$1.8M
Suppression of IgE-Mediated Disease by Polyclonal Rapid DesensitizationR01AI113162 · NIAID · UNIVERSITY OF CINCINNATI · PI FINKELMAN, FRED DOUGLASS · 2014 to 2017
$1.6M
Axl receptor tyrosine kinase, a potential therapeutic target in glomerulonephritisR01DK116789 · NIDDK · UNIVERSITY OF CINCINNATI · PI SHAO, WEN-HAI · 2019 to 2021
$710k
NIAID NIH HHS R01 AI113162NIAID NIH HHS R01 AI130103NIAID NIH HHS R01 AI145991NIDDK NIH HHS P30 DK078392NIDDK NIH HHS R01 DK116789
6 · The paper itself

Abstract

backgroundMast cell and basophil activation by antigen cross-linking of FcεRI-bound IgE is central to allergy pathogenesis. We previously demonstrated global suppression of this process by rapid desensitization with anti-FcεRIα mAbs.

objectivesWe sought to determine whether use of monovalent (mv) anti-FcεRIα mAbs increases desensitization safety without loss of efficacy.

methodsmv anti-human (hu) FcεRIα mAbs were produced with mouse-derived immunoglobulin variable regions and huIgG

resultsmv anti-hu FcεRIα mAbs are considerably less able than divalent mAbs are to induce anaphylaxis and deplete mast cell and basophil IgE, but mv mAbs still strongly suppress IgE-mediated disease. The mv mAbs can be safely administered as a single large dose to mice with typical susceptibility to anaphylaxis, while a rapid desensitization approach safely suppresses disease in mice with increased susceptibility. Our huIgG

conclusionsmv anti-FcεRIα mAbs more safely suppress IgE-mediated anaphylaxis and food allergy than divalent variants of the same mAbs do. These mv mAbs may be useful for suppression of huIgE-mediated disease.

Indexed as

AnaphylaxisAnimalsAnti-Allergic AgentsAntibodies, MonoclonalFemaleFood HypersensitivityImmunoglobulin EImmunoglobulin GMaleMast CellsMiceMice, Inbred BALB CMice, TransgenicPhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesReceptors, IgESyk KinaseAnti-Allergic AgentsAntibodies, MonoclonalImmunoglobulin EImmunoglobulin GInpp5d protein, mousePhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesReceptors, IgESyk KinaseSyk protein, mousecross-linkingdesensitizationhumanizedIgG(1)IgG(4)IL-4mast cellMouseSyk

Identifiers

PMID33326804
PMCPMC8215870
OpenAlexW3111561572

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.