Evidence map›Paper›PMID 15520848›Full record

ReviewThe Journal of clinical investigation2004

An integrated view of suppressor T cell subsets in immunoregulation.

Hong Jiang, Leonard Chess

Abstract readReview
In one paragraph

Review in The Journal of clinical investigation, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

70 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. NY-ESO-1 DNA vaccine induces T-cell responses that are suppressed by regulatory T cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2009
    Trial
  4. Trial
  5. Article
  6. Review
  7. Review
  8. Observational
  9. Relationship between expression mRNA gene Treg, Treg, CD4Annals of medicine and surgery (2012) · 2021
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Attenuation ofGut pathogens · 2017
    Article
  18. Role of cellular events in the pathophysiology of sepsis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2016
    Review
  19. Multiple Sclerosis and T Lymphocytes: An Entangled Story.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2015
    Review
  20. Article

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

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

2 authors.

Hong JiangDepartment of Medicine and Pathology, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.
Leonard Chess

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
IMMUNE RESPONSES BY TCR VB SPECIFIC CD8 T CELLSR29AI039630 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JIANG, HONG · 1996 to 2000
$121k
SDF1 IN MESENCHYMAL ALTERATIONS OF IMMUNE INJURYP01AI039675 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHESS, LEONARD · 1996 to 1999
–
NIAID NIH HHS AI39630NIAID NIH HHS AI39675NIAID NIH HHS U19 AI046132NIAID NIH HHS U19 AI/46132
6 · The paper itself

Abstract

The immune system evolved to protect organisms from a virtually infinite variety of disease-causing agents but to avoid harmful responses to self. Because immune protective mechanisms include the elaboration of potent inflammatory molecules, antibodies, and killer cell activation--which together can not only destroy invading microorganisms, pathogenic autoreactive cells, and tumors, but also mortally injure normal cells--the immune system is inherently a "double-edged sword" and must be tightly regulated. Immune response regulation includes homeostatic mechanisms intrinsic to the activation and differentiation of antigen-triggered immunocompetent cells and extrinsic mechanisms mediated by suppressor cells. This review series will focus on recent advances indicating that distinct subsets of regulatory CD4+ and CD8+ T cells as well as NK T cells control the outgrowth of potentially pathogenic antigen-reactive T cells and will highlight the evidence that these suppressor T cells may play potentially important clinical roles in preventing and treating immune-mediated disease. Here we provide a historical overview of suppressor cells and the experimental basis for the existence of functionally and phenotypically distinct suppressor subsets. Finally, we will speculate on how the distinct suppressor cell subsets may function in concert to regulate immune responses.

Indexed as

Immune SystemAnimalsApoptosisCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesGenes, DominantHistocompatibility Antigens Class IHumansKiller Cells, NaturalLymphocyte SubsetsModels, BiologicalPhenotypeReceptors, Interleukin-2T-Lymphocytes, RegulatoryHistocompatibility Antigens Class IQ surface antigensReceptors, Interleukin-2

Identifiers

PMID15520848
PMCPMC524238

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.