Evidence map›Paper›PMID 19156219›Full record

ArticlePloS one2009

Human cord blood stem cell-modulated regulatory T lymphocytes reverse the autoimmune-caused type 1 diabetes in nonobese diabetic (NOD) mice.

Yong Zhao, Brian Lin, Robert Darflinger, Yongkang Zhang, Mark J Holterman, Randal A Skidgel

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.6field-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.

NCT01350219 phase2unknown statusnot on this mapstarted 2010, after this paper: background citation

Phase 2 Study of Stem Cell Educator Therapy in Type 1 Diabetes

TypeinterventionalSponsorThrone Biotechnologies Inc.Ran2010 to 2019Enrolled100ConditionsType 1 DiabetesArmsStem Cell Educator
NCT01415726 phase1 / phase2completednot on this mapstarted 2011, after this paper: background citation

Stem Cell Educator Therapy in Type 2 Diabetes

TypeinterventionalSponsorUniversity of Illinois at ChicagoRan2011 to 2012Enrolled25ConditionsType 2 DiabetesArmsStem Cell Educator
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 78 citations in OpenAlex.

  1. Trial
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  6. Immunomodulation for Tissue Repair and Regeneration.Tissue engineering and regenerative medicine · 2023
    Review
  7. Article
  8. Review
  9. Further comments on the role of ACE-2 positive macrophages in human lung.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2023
    Article
  10. Review
  11. Review
  12. Therapeutic Advances in Diabetes, Autoimmune, and Neurological Diseases.International journal of molecular sciences · 2021
    Review
  13. Review
  14. Review
  15. Existence of Circulating Mitochondria in Human and Animal Peripheral Blood.International journal of molecular sciences · 2020
    Article
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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

6 authors at 1 institution in 1 country.

Yong ZhaoDepartment of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States of America. yongzhao@uic.edu
Brian Lin
Robert Darflinger
Yongkang Zhang
Mark J Holterman
Randal A Skidgel
University of Illinois Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe deficit of pancreatic islet beta cells caused by autoimmune destruction is a crucial issue in type 1 diabetes (T1D). It is essential to fundamentally control the autoimmunity for treatment of T1D. Regulatory T cells (Tregs) play a pivotal role in maintaining self-tolerance through their inhibitory impact on autoreactive effector T cells. An abnormality of Tregs is associated with initiation of progression of T1D. METHODOLOGY/PRINCIPAL

findingsHere, we report that treatment of established autoimmune-caused diabetes in NOD mice with purified autologous CD4(+)CD62L(+) Tregs co-cultured with human cord blood stem cells (CB-SC) can eliminate hyperglycemia, promote islet beta-cell regeneration to increase beta-cell mass and insulin production, and reconstitute islet architecture. Correspondingly, treatment with CB-SC-modulated CD4(+)CD62L(+) Tregs (mCD4CD62L Tregs) resulted in a marked reduction of insulitis, restored Th1/Th2 cytokine balance in blood, and induced apoptosis of infiltrated leukocytes in pancreatic islets. CONCLUSIONS/SIGNIFICANCE: These data demonstrate that treatment with mCD4CD62L Tregs can reverse overt diabetes, providing a novel strategy for the treatment of type 1 diabetes as well as other autoimmune diseases.

Indexed as

AnimalsApoptosisCD4-Positive T-LymphocytesCytokinesDiabetes Mellitus, Type 1Disease ProgressionFemaleFetal BloodHyperglycemiaIslets of LangerhansL-SelectinMiceMice, Inbred NODStem CellsT-Lymphocytes, RegulatoryCytokinesL-Selectin

Identifiers

PMID19156219
PMCPMC2627485
OpenAlexW2100481486

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.