Evidence map›Paper›PMID 24472603›Full record

ReviewImmunology letters2014

B cells and type 1 diabetes ...in mice and men.

Rochelle M Hinman, Mia J Smith, John C Cambier

Open access · greenAbstract readReview
In one paragraph

Review in Immunology letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Advanced Delivery Strategies for Immunotherapy in Type I Diabetes Mellitus.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Influence ofFrontiers in immunology · 2021
    Review
  10. Article
  11. Article
  12. The diabetes pandemic and associated infections: suggestions for clinical microbiology.Reviews in medical microbiology : a journal of the Pathological Society of Great Britain and Ireland · 2019
    Article
  13. Review
  14. Article
  15. Heterogeneity of B Cell Functions in Stroke-Related Risk, Prevention, Injury, and Repair.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2016
    Review
  16. Article
  17. 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

3 authors at 2 institutions in 1 country.

Rochelle M HinmanUniversity of Colorado Denver and National Jewish Health, Denver, CO, United States. Electronic address: rochelle.hinman@ucdenver.edu.
Mia J SmithUniversity of Colorado Denver and National Jewish Health, Denver, CO, United States. Electronic address: mia.smith@ucdenver.edu.
John C CambierUniversity of Colorado Denver and National Jewish Health, Denver, CO, United States; Department of Immunology, National Jewish Health, Rm 803A, Goodman Building, 1400 Jackson Street, Denver, CO 80206, United States. Electronic address: cambierj@njhealth.org.
National Jewish Health · USUniversity of Colorado Denver · US

Funding

Molecular Mechanisms of Immune ToleranceT32AI074491 · NIAID · NATIONAL JEWISH HEALTH · PI CAMBIER, JOHN C, PELANDA, ROBERTA · 2009 to 2023
$4.1M
SIGNAL TRANSDUCTION IN B CELL ACTIVATIONR01AG013983 · NIA · UNIVERSITY OF COLORADO DENVER · PI CAMBIER, JOHN C · 1996 to 2010
$3.0M
MOLECULAR BIOLOGY OF B CELL TOLERANCE AND ACTIVATIONR01AI020519 · NIAID · UNIVERSITY OF COLORADO DENVER · PI CAMBIER, JOHN C. · 1985 to 2007
$2.3M
B Cells and Type 1 DiabetesR01DK096492 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI CAMBIER, JOHN C · 2012 to 2016
$1.6M
NIAID NIH HHS R01 AI020519NIA NIH HHS R01 AG013983NIDDK NIH HHS R01 DK096492
6 · The paper itself

Abstract

Nearly 70% of newly produced B cells express autoreactive antigen receptors and must be silenced to prevent autoimmunity. Failure of silencing mechanisms is apparent in type 1 diabetes (T1D), where islet antigen-specific B cells appear critical for development of disease. Evidence for a B cell role in T1D includes success of B cell targeted anti-CD20 therapy, which delays T1D progression in both NOD mice and new onset patients. Demonstrating the importance of specificity, NOD mice whose B cell repertoire is biased toward insulin reactivity show increased disease development, while bias away from insulin reactivity largely prevents disease. Finally, though not required for illness, high affinity insulin autoantibodies are often the first harbingers of T1D. B cell cytokine production and auto-antigen presentation to self-reactive T cells are likely important in pathogenesis. Here we review B cell function, as described above, in T1D in humans and the non-obese diabetic (NOD) mouse. We will discuss recent broad-based B cell depletion studies and how they may provide the basis for refinement of future treatments for the disorder.

Indexed as

Molecular Targeted TherapyAnimalsAntibodies, Monoclonal, Murine-DerivedAntigens, CD20AutoantibodiesB-LymphocytesDiabetes Mellitus, Type 1Gene ExpressionHumansInsulinIslets of LangerhansLymphocyte DepletionMiceMice, Inbred NODReceptors, Antigen, B-CellRituximabAntibodies, Monoclonal, Murine-DerivedAntigens, CD20AutoantibodiesInsulinReceptors, Antigen, B-CellRituximabAutoimmunityB lymphocytesType 1 diabetes (T1D)

Identifiers

PMID24472603
PMCPMC5526342
OpenAlexW2071632755

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.