Evidence map›Paper›PMID 34216934›Full record

ReviewCurrent opinion in immunology2021

Intrinsic and extrinsic regulation of IgE B cell responses.

Adam K Wade-Vallance, Christopher D C Allen

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2021. 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
3.2field-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

23 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Whence and wherefore IgE?Immunological reviews · 2024
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. B cell receptor ligation induces IgE plasma cell elimination.The Journal of experimental medicine · 2023
    Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Features of B Cell Responses Relevant to Allergic Disease.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Review
  20. Review
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

2 authors at 1 institution in 1 country.

Adam K Wade-VallanceBiomedical Sciences Graduate Program, University of California, San Francisco, San Francisco, CA 94143, USA; Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94143, USA; Sandler Asthma Basic Research Center, University of California, San Francisco, San Francisco, CA 94143, USA.
Christopher D C AllenCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94143, USA; Sandler Asthma Basic Research Center, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Anatomy, University of California, San Francisco, San Francisco, CA 94143, USA. Electronic address: Chris.Allen@ucsf.edu.
University of California, San Francisco · US

Funding

Regulation of IgE responses by B cell receptor signalingR01AI130470 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ALLEN, CHRISTOPHER DAVID CABALLERO · 2018 to 2022
$2.0M
Molecular basis for the regulation of IgE class switch recombination by IL-21 and STAT3R21AI154335 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ALLEN, CHRISTOPHER DAVID CABALLERO · 2021 to 2022
$433k
CIHR DFD–170769NIAID NIH HHS R01 AI130470NIAID NIH HHS R21 AI154335
6 · The paper itself

Abstract

Stringent regulation of IgE antibody production is critical for constraining allergic responses. This review discusses recent advances in understanding cell-intrinsic and extrinsic mechanisms that regulate the genesis and fate of IgE B cells. B cell-intrinsic regulation of IgE is orchestrated by the IgE B Cell Receptor (BCR). Through its antigen-independent signaling and low surface expression, the IgE BCR drives IgE B cells to differentiate into short-lived plasma cells and/or undergo apoptosis, restricting IgE-expressing cells from entering long-lived compartments. The pivotal extrinsic regulators of IgE responses are T follicular helper cells (T

Indexed as

ImmunomodulationAnimalsAntibody FormationApoptosisB-LymphocytesCytokinesDisease SusceptibilityGene Expression RegulationGerminal CenterHumansHypersensitivityImmunoglobulin EImmunologic MemoryPlasma CellsReceptors, Antigen, B-CellCytokinesImmunoglobulin EReceptors, Antigen, B-Cell

Identifiers

PMID34216934
PMCPMC9262376
OpenAlexW3175388691

What OpenQuestion holds

Textmetadata
LicenceTDM
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.