Evidence map›Paper›PMID 18060033›Full record

ArticleThe Journal of clinical investigation2007

Treatment with CD20-specific antibody prevents and reverses autoimmune diabetes in mice.

Chang-yun Hu, Daniel Rodriguez-Pinto, Wei Du, Anupama Ahuja, Octavian Henegariu, F Susan Wong, Mark J Shlomchik, Li Wen

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 209 papers.

0numbers the graph read from it
0cells of the map it votes in
209citing papers in PubMed
21.6field-weighted citation impact, top 1% 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

209 citing papers in PubMed, 419 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Altered B cell metabolic pathways characterize type 1 diabetes progression.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Interleukin-1 signaling and CD4Frontiers in immunology · 2025
    Article
  11. Article
  12. Article
  13. Advancing Animal Models of Human Type 1 Diabetes.Cold Spring Harbor perspectives in medicine · 2024
    Review
  14. Article
  15. The immunology of type 1 diabetes.Nature reviews. Immunology · 2024
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Chang-yun HuSection of Endocrinology, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut 06520, USA.
Daniel Rodriguez-Pinto
Wei Du
Anupama Ahuja
Octavian Henegariu
F Susan Wong
Mark J Shlomchik
Li Wen
University of Bristol · GBYale University · US

Funding

Yale Diabetes Research CenterP30DK045735 · NIDDK · YALE UNIVERSITY · PI Kevan C Herold, GERALD I SHULMAN · 1993 to 2026
$44.0M
THE ROLE OF B CELLS IN LUPUS NEPHRITIS AND VASCULITISR01AR044077 · NIAMS · YALE UNIVERSITY · PI SHLOMCHIK, MARK J · 1997 to 2016
$6.2M
NIAMS NIH HHS R01 AR044077NIAMS NIH HHS R01-AR44077NIDDK NIH HHS P30 DK045735NIDDK NIH HHS P30-DK-45735
6 · The paper itself

Abstract

The precise roles of B cells in promoting the pathogenesis of type 1 diabetes remain undefined. Here, we demonstrate that B cell depletion in mice can prevent or delay diabetes, reverse diabetes after frank hyperglycemia, and lead to the development of cells that suppress disease. To determine the efficacy and potential mechanism of therapeutic B cell depletion, we generated a transgenic NOD mouse expressing human CD20 (hCD20) on B cells. A single cycle of treatment with an antibody specific for hCD20 temporarily depleted B cells and significantly delayed and/or reduced the onset of diabetes. Furthermore, disease established to the point of clinical hyperglycemia could be reversed in over one-third of diabetic mice. Why B cell depletion is therapeutic for a variety of autoimmune diseases is unclear, although effects on antibodies, cytokines, and antigen presentation to T cells are thought to be important. In B cell-depleted NOD mice, we identified what we believe is a novel mechanism by which B cell depletion may lead to long-term remission through expansion of Tregs and regulatory B cells. Our results demonstrate clinical efficacy even in established disease and identify mechanisms for therapeutic action that will guide design and evaluation of parallel studies in patients.

Indexed as

Lymphocyte DepletionAnimalsAntibodies, MonoclonalAntigen PresentationAntigens, CD20AutoantibodiesB-LymphocytesCytokinesDiabetes Mellitus, Type 1HumansHyperglycemiaMiceMice, Inbred NODMice, SCIDMice, TransgenicT-Lymphocytes, RegulatoryAntibodies, MonoclonalAntigens, CD20AutoantibodiesCytokines

Identifiers

PMID18060033
PMCPMC2096456
OpenAlexW1997452174

What OpenQuestion holds

Textmetadata
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.