Evidence map›Paper›PMID 22143888›Full record

ArticleThe Journal of experimental medicine2011

Immature B cells preferentially switch to IgE with increased direct Sμ to Sε recombination.

Duane R Wesemann, Jennifer M Magee, Cristian Boboila, Dinis Pedro Calado, Michael P Gallagher, Andrew J Portuguese, John P Manis, Xiaolong Zhou, Mike Recher, Klaus Rajewsky and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

65 citing papers in PubMed, 105 citations in OpenAlex.

  1. Review
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  3. Review
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  7. Article
  8. Whence and wherefore IgE?Immunological reviews · 2024
    Review
  9. Review
  10. Article
  11. Induction of natural IgE by glucocorticoids.The Journal of experimental medicine · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. CtIP-mediated DNA resection is dispensable for IgH class switch recombination by alternative end-joining.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  19. Review
  20. Article

5 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Duane R WesemannProgram in Cellular and Molecular Medicine and Immune Disease Institute, Children's Hospital Boston, MA 02115, USA.
Jennifer M Magee
Cristian Boboila
Dinis Pedro Calado
Michael P Gallagher
Andrew J Portuguese
John P Manis
Xiaolong Zhou
Mike Recher
Klaus Rajewsky
Luigi D Notarangelo
Frederick W Alt
Boston Children's Hospital · USHoward Hughes Medical Institute · USHarvard University · US

Funding

Role of TACI mutations in CVIDP01AI076210 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TERHORST, CORNELIS P · 2009 to 2013
$9.0M
Mechanisms that Regulate Antibody Class Switch Recombination and Somatic HypermutationR37AI077595 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI Frederick W. Alt · 2019 to 2026
$4.6M
Molecular Mechanisms of Class Switch RecombinationR01AI077595 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI ALT, FREDERICK W. · 2009 to 2018
$4.3M
Peripheral B Cell Receptor EditingK08AI089972 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI WESEMANN, DUANE R. · 2010 to 2014
$685k
DNA Damage Responses in B Cell DevelopmentR21CA133781 · NCI · BOSTON CHILDREN'S HOSPITAL · PI MANIS, JOHN P · 2009 to 2010
$407k
Howard Hughes Medical InstituteNCI NIH HHS R21 CA133781NIAID NIH HHS 5P01AI076210-02NIAID NIH HHS AI076210NIAID NIH HHS AI077595NIAID NIH HHS K08 AI089972NIAID NIH HHS K08AI89972NIAID NIH HHS P01 AI076210NIAID NIH HHS R01 AI077595NIAID NIH HHS R37 AI077595
6 · The paper itself

Abstract

Immunoglobulin heavy chain (IgH) class-switch recombination (CSR) replaces initially expressed Cμ (IgM) constant regions (C(H)) exons with downstream C(H) exons. Stimulation of B cells with anti-CD40 plus interleukin-4 induces CSR from Cμ to Cγ1 (IgG1) and Cε (IgE), the latter of which contributes to the pathogenesis of atopic diseases. Although Cε CSR can occur directly from Cμ, most mature peripheral B cells undergo CSR to Cε indirectly, namely from Cμ to Cγ1, and subsequently to Cε. Physiological mechanisms that influence CSR to Cγ1 versus Cε are incompletely understood. In this study, we report a role for B cell developmental maturity in IgE CSR. Based in part on a novel flow cytometric IgE CSR assay, we show that immature B cells preferentially switch to IgE versus IgG1 through a mechanism involving increased direct CSR from Cμ to Cε. Our findings suggest that IgE dysregulation in certain immunodeficiencies may be related to impaired B cell maturation.

Indexed as

AnimalsB-LymphocytesCommon Variable ImmunodeficiencyImmunoglobulin Class SwitchingImmunoglobulin EImmunoglobulin epsilon-ChainsImmunoglobulin GImmunoglobulin mu-ChainsMiceMice, KnockoutRecombination, GeneticImmunoglobulin EImmunoglobulin epsilon-ChainsImmunoglobulin GImmunoglobulin mu-Chains

Identifiers

PMID22143888
PMCPMC3244039
OpenAlexW2140323047

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.