Evidence map›Paper›PMID 19502979›Full record

ReviewCurrent opinion in endocrinology, diabetes, and obesity2009

Change you can B(cell)eive in: recent progress confirms a critical role for B cells in type 1 diabetes.

Shannon K O'Neill, Edwin Liu, John C Cambier

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in endocrinology, diabetes, and obesity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Advances in the cellular immunological pathogenesis of type 1 diabetes.Journal of cellular and molecular medicine · 2014
    Review
  6. Article
  7. Article
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  12. Article
  13. Article
  14. Indications of rituximab in autoimmune diseases.Drug discovery today. Therapeutic strategies · 2009
    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

3 authors at 2 institutions in 1 country.

Shannon K O'NeillUniversity of Colorado Denver and National Jewish Health, 1400 Jackson Street, Denver, Colorado 80206, USA.
Edwin Liu
John C Cambier
University of Colorado Denver · USNational Jewish Health · US

Funding

THE REGULATION OF V ALPHA 7 EXPRESSING T CELLSP01AI022295 · NIAID · NATIONAL JEWISH HEALTH · PI CAMBIER, JOHN C · 1985 to 2011
$11.7M
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
NIAID NIH HHS P01 AI022295NIAID NIH HHS R01 AI020519NIA NIH HHS R01 AG013983
6 · The paper itself

Abstract

purpose of reviewHere we review extant recent findings regarding the multiple roles of B cells in type 1 diabetes (T1D) and discuss how autoreactive B cells may become activated by a breach in B cell tolerance, and thereby initiate disease. Finally, we discuss the use of B cell-targeted therapies for treatment of autoimmunity. RECENT

findingsAnti-CD20-specific depletion of B cells prevents and reverses diabetes in human CD20/non-obese diabetic (NOD) mice. Correspondingly, in nontransgenic NOD mice, B cells are effectively depleted with high dose antimouse CD20 mAbs of varying isotypes, and this also prevents diabetes in more than 60% of the mice when administered early, and significantly delays disease in 15-week-old animals. A separate study revealed that targeting B cells with anti-CD22/cal monoclonal antibody therapy delays diabetes onset in prediabetic NOD mice and restores normoglycemia in new-onset hyperglycemic NOD mice. In humans, a clinical trial of rituximab in new onset type 1 diabetics has yielded promising preliminary findings. SUMMARY: B cells are major players in T1D in humans, and clearly essential for disease development in the NOD mouse model of T1D. In this review, we discuss the silencing of autoreactive B cells and how failure of this process may contribute to autoimmunity. Further, we describe the most recent advances in studies of therapeutic effects of B cell depletion in T1D, and provide recent data indicating the diverse functions by which B cells may mediate disease.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CD20B-LymphocytesDiabetes Mellitus, Type 1HumansMiceMice, Inbred NODSialic Acid Binding Ig-like Lectin 2Antibodies, MonoclonalAntigens, CD20Sialic Acid Binding Ig-like Lectin 2

Identifiers

PMID19502979
PMCPMC2968699
OpenAlexW2072136242

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.