Evidence map›Paper›PMID 23810240›Full record

ArticleThe Journal of allergy and clinical immunology2013

Rapid desensitization induces internalization of antigen-specific IgE on mouse mast cells.

Tatsuya Oka, Eon J Rios, Mindy Tsai, Janet Kalesnikoff, Stephen J Galli

Open access · greenAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

40 citing papers in PubMed, 95 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Temporal Modulation of Drug Desensitization Procedures.Current issues in molecular biology · 2022
    Review
  10. Desensitization for the prevention of drug hypersensitivity reactions.The Korean journal of internal medicine · 2022
    Review
  11. Review
  12. Findings ofFrontiers in allergy · 2022
    Article
  13. Review
  14. Oral Immunotherapy for Children with Cow's Milk Allergy.Pathogens (Basel, Switzerland) · 2021
    Review
  15. Article
  16. Article
  17. Mechanisms of oral immunotherapy.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2021
    Review
  18. Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Tatsuya OkaDepartment of Pathology, Stanford University School of Medicine, Stanford, Calif.
Eon J Rios
Mindy Tsai
Janet Kalesnikoff
Stephen J Galli
Stanford University · US

Funding

Role of Mast Cells in Inflammation and ImmunityR01CA072074 · NCI · STANFORD UNIVERSITY · PI GALLI, STEPHEN JOSEPH · 1996 to 2010
$4.4M
Expression and Modulation of Mast Cell Function in AsthmaR01AI070813 · NIAID · STANFORD UNIVERSITY · PI GALLI, STEPHEN JOSEPH · 2006 to 2010
$2.5M
Regulation of Mast Cell Development and FunctionR01AI023990 · NIAID · STANFORD UNIVERSITY · PI GALLI, STEPHEN JOSEPH · 1986 to 2010
$2.4M
REGULATION OF MAST CELL DEVELOPMENT &FUNCTIONR37AI023990 · NIAID · STANFORD UNIVERSITY · PI GALLI, STEPHEN J · 1996 to 2005
$2.2M
NCI NIH HHS CA072074NCI NIH HHS R01 CA072074NIAID NIH HHS AI023990NIAID NIH HHS AI070813NIAID NIH HHS AI072074NIAID NIH HHS R01 AI023990NIAID NIH HHS R01 AI070813NIAID NIH HHS R37 AI023990
6 · The paper itself

Abstract

backgroundRapid desensitization transiently prevents severe allergic reactions, allowing administration of life-saving therapies in previously sensitized patients. However, the mechanisms underlying successful rapid desensitization are not fully understood.

objectivesWe sought to investigate whether the mast cell (MC) is an important target of rapid desensitization in mice sensitized to exhibit IgE-dependent passive systemic anaphylaxis in vivo and to investigate the antigen specificity and underlying mechanisms of rapid desensitization in our mouse model.

methodsC57BL/6 mice (in vivo) or primary isolated C57BL/6 mouse peritoneal mast cells (PMCs; in vitro) were passively sensitized with antigen-specific anti-2,4-dinitrophenyl IgE, anti-ovalbumin IgE, or both. MCs were exposed over a short period of time to increasing amounts of antigen (2,4-dinitrophenyl-human serum albumin or ovalbumin) in the presence of extracellular calcium in vitro or by means of intravenous administration to sensitized mice in vivo before challenging the mice with or exposing the PMCs to optimal amounts of specific or irrelevant antigen.

resultsRapidly exposing mice or PMCs to progressively increasing amounts of specific antigen inhibited the development of antigen-induced hypothermia in sensitized mice in vivo and inhibited antigen-induced PMC degranulation and prostaglandin D2 synthesis in vitro. Such MC hyporesponsiveness was induced antigen-specifically and was associated with a significant reduction in antigen-specific IgE levels on MC surfaces.

conclusionsRapidly exposing MCs to progressively increasing amounts of antigen can both enhance the internalization of antigen-specific IgE on the MC surface and also desensitize these cells in an antigen-specific manner in vivo and in vitro.

Indexed as

2,4-DinitrophenolAnaphylaxisAnimalsAntibodies, Anti-IdiotypicAntibody SpecificityAntigensDesensitization, ImmunologicHumansHypersensitivityImmunoglobulin EMast CellsMiceMice, Inbred C57BLOvalbuminTime Factors2,4-DinitrophenolAntibodies, Anti-IdiotypicAntigensanti-IgE antibodiesImmunoglobulin EOvalbumin2,4-DinitrophenylAnaphylaxisantigenbasophilBMCMCBone marrow–derived cultured mast celldegranulationdesensitizationDNPFITCFluorescein isothiocyanateHSAHuman serum albuminIgEmast cellMast cellMast cell protease 1MCMCPT-1Mean fluorescence intensityMFIOVAOvalbuminPassive systemic anaphylaxisPeritoneal mast cellPGD(2)PMCProstaglandin D(2)PSArapid desensitizationreceptor internalizationrush desensitizationSignal transducer and activator of transcription 6STAT6

Identifiers

PMID23810240
PMCPMC3789647
OpenAlexW2018878565

What OpenQuestion holds

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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.