Evidence map›Paper›PMID 11696599›Full record

ArticleThe Journal of experimental medicine2001

Hyper immunoglobulin E response in mice with monoclonal populations of B and T lymphocytes.

M A Curotto de Lafaille, S Muriglan, M J Sunshine, Y Lei, N Kutchukhidze, G C Furtado, A K Wensky, D Olivares-Villagómez, J J Lafaille

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

39 citing papers in PubMed, 107 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Microbial symbionts regulate the primary Ig repertoire.The Journal of experimental medicine · 2018
    Article
  7. Article
  8. Article
  9. Review
  10. Regulatory T cells in allergic diseases.The Journal of allergy and clinical immunology · 2016
    Review
  11. Article
  12. Article
  13. Antiallergic Effects of Trichostatin A in a Murine Model of Allergic Rhinitis.Clinical and experimental otorhinolaryngology · 2015
    Article
  14. Article
  15. Article
  16. Polyclonal hyper-IgE mouse model reveals mechanistic insights into antibody class switch recombination.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  17. Article
  18. Activator protein 1 suppresses antitumor T-cell function via the induction of programmed death 1.Proceedings of the National Academy of Sciences of the United States of America · 2012
    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

9 authors at 2 institutions in 1 country.

M A Curotto de LafailleProgram of Molecular Pathogenesis, Skirball Institute for Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA.
S Muriglan
M J Sunshine
Y Lei
N Kutchukhidze
G C Furtado
A K Wensky
D Olivares-Villagómez
J J Lafaille
Institute for Molecular Medicine · USNew York University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A key event in the pathogenesis of allergies is the production of antibodies of the immunoglobulin (Ig)E class. In normal individuals the levels of IgE are tightly regulated, as illustrated by the low serum IgE concentration. In addition, multiple immunizations are usually required to generate detectable IgE responses in normal experimental animals. To define the parameters that regulate IgE production in vivo, we generated mice bearing monoclonal populations of B and T lymphocytes specific for influenza virus hemagglutinin (HA) and chicken ovalbumin (OVA), respectively. A single immunization of the monoclonal mice with the cross-linked OVA-HA antigen led to serum IgE levels that reached 30-200 microg/ml. This unusually high IgE response was prevented by the infusion of regulatory alpha/beta CD4(+) T cells belonging to both CD25(+) and CD25(-) subpopulations. The regulation by the infused T cells impeded the development of fully competent OVA-specific effector/memory Th2 lymphocytes without inhibiting the initial proliferative response of T cells or promoting activation-induced cell death. Our results indicate that hyper IgE responses do not occur in normal individuals due to the presence of regulatory T cells, and imply that the induction of regulatory CD4(+) T cells could be used for the prevention of atopy.

Indexed as

AnimalsAntigensB-LymphocytesChickensFemaleGerminal CenterHemagglutinin Glycoproteins, Influenza VirusImmunoglobulin EMaleMiceMice, Inbred BALB CModels, ImmunologicalOvalbuminTh2 CellsT-LymphocytesAntigensHemagglutinin Glycoproteins, Influenza VirusImmunoglobulin EOvalbumin

Identifiers

PMID11696599
PMCPMC2195981
OpenAlexW2150473534

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.