Evidence map›Paper›PMID 20877010›Full record

ArticleThe Journal of clinical investigation2010

HLA-E-restricted regulatory CD8(+) T cells are involved in development and control of human autoimmune type 1 diabetes.

Hong Jiang, Steve M Canfield, Mary P Gallagher, Hong H Jiang, Yihua Jiang, Zongyu Zheng, Leonard Chess

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

72 citing papers in PubMed, 108 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Review
  6. CD8+ Regulatory T Cells.Annual review of immunology · 2026
    Review
  7. Donor-derived CD8bioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Article
  10. Review
  11. Cell Therapy for Type 1 Diabetes Mellitus: a Review of Clinical Trials.Bulletin of experimental biology and medicine · 2025
    Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. An angel or a devil? Current view on the role of CD8Journal of translational medicine · 2024
    Review
  17. Review
  18. Article
  19. Review
  20. Human CD8Immune network · 2023
    Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Hong JiangDepartment of Medicine, Naomi Berrie Diabetes Center (NBDC), Columbia University, College of Physicians and Surgeons, New York, New York 10032, USA. hj4@columbia.edu
Steve M Canfield
Mary P Gallagher
Hong H Jiang
Yihua Jiang
Zongyu Zheng
Leonard Chess
Columbia University · US

Funding

T cell activation and repertoire in insulin dependent diabetes / anti CD40L trialU19AI046132 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHESS, LEONARD · 1999 to 2007
$6.5M
CD8+ T cells Control Autoimmunity in EAER01AI065609 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JIANG, HONG · 2006 to 2007
$793k
NIAID NIH HHS R01 AI065609NIAID NIH HHS U19 AI046132NIAID NIH HHS U19 AI46132
6 · The paper itself

Abstract

A key feature of the immune system is its ability to discriminate self from nonself. Breakdown in any of the mechanisms that maintain unresponsiveness to self (a state known as self-tolerance) contributes to the development of autoimmune conditions. Recent studies in mice show that CD8(+) T cells specific for the unconventional MHC class I molecule Qa-1 bound to peptides derived from the signal sequence of Hsp60 (Hsp60sp) contribute to self/nonself discrimination. However, it is unclear whether they exist in humans and play a role in human autoimmune diseases. Here we have shown that CD8(+) T cells specific for Hsp60sp bound to HLA-E (the human homolog of Qa-1) exist and play an important role in maintaining peripheral self-tolerance by discriminating self from nonself in humans. Furthermore, in the majority of type 1 diabetes (T1D) patients tested, there was a specific defect in CD8(+) T cell recognition of HLA-E/Hsp60sp, which was associated with failure of self/nonself discrimination. However, the defect in the CD8(+) T cells from most of the T1D patients tested could be corrected in vitro by exposure to autologous immature DCs loaded with the Hsp60sp peptide. These data suggest that HLA-E-restricted CD8(+) T cells may play an important role in keeping self-reactive T cells in check. Thus, correction of this defect could be a potentially effective and safe approach in the therapy of T1D.

Indexed as

Amino Acid SequenceCD8-Positive T-LymphocytesCell LineChaperonin 60Diabetes Mellitus, Type 1Histocompatibility Antigens Class IHLA AntigensHLA-E AntigensHumansMolecular Sequence DataT-Lymphocytes, RegulatoryChaperonin 60Histocompatibility Antigens Class IHLA AntigensHLA-E Antigens

Identifiers

PMID20877010
PMCPMC2947239
OpenAlexW2037309674

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.