Evidence map›Paper›PMID 19426214›Full record

ReviewImmunological reviews2009

Regulating the regulators: costimulatory signals control the homeostasis and function of regulatory T cells.

Hélène Bour-Jordan, Jeffrey A Bluestone

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 122 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 3% 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

122 citing papers in PubMed, 1 synthesis or guideline pooled it, 224 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Annals of surgical treatment and research · 2024
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review

62 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 at 1 institution in 1 country.

Hélène Bour-JordanUCSF Diabetes Center, University of California at San Francisco, San Francisco, CA, USA.
Jeffrey A Bluestone
University of California, San Francisco · US

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI MARK W. LINGEN · 1985 to 2026
$122.1M
Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRUMMEL, MATTHEW F · 2003 to 2019
$21.8M
Src tyrosine kinases and autoimmunity.P01AI035297 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ABBAS, ABUL K. · 1993 to 2010
$16.5M
Spontaneous Autoimmune Model of Peripheral NeuropathyR01AI050834 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLUESTONE, JEFFREY A · 2002 to 2011
$3.1M
MECHANISMS OF T CELL TOLERANCE IN CD28-DEFICIENT MICEP01AI035294 · NIAID · UNIVERSITY OF CHICAGO · PI BLUESTONE, JEFFREY A · 1993 to 2000
$750k
REGULATION OF BETA CELL DEATH IN THE PATHOGENESIS OF IDDMP01DK049799 · NIDDK · UNIVERSITY OF CHICAGO · PI SANT, ANDREA JANINE · 1995 to 1999
–
NCI NIH HHS P30 CA014599NIAID NIH HHS P01 AI035294NIAID NIH HHS P01 AI035297NIAID NIH HHS R01 AI050834NIDDK NIH HHS P01 DK049799NIDDK NIH HHS P30 DK063720
6 · The paper itself

Abstract

summaryCostimulation is a concept that goes back to the early 1980s when Lafferty and others hypothesized that cell surface and soluble molecules must exist that are essential for initiating immune responses subsequent to antigen exposure. The explosion in this field of research ensued as over a dozen molecules have been identified to function as second signals following T-cell receptor engagement. By 1994, it seemed clear that the most prominent costimulatory pathway CD28 and functionally related costimulatory molecules, such as CD154, were the major drivers of a positive immune response. Then the immunology world turned upside down. CD28 knockout mice, which were, in most cases, immunodeficient, led to increased autoimmunity when bred into the non-obese diabetic background. Another CD28 family member, cytotoxic T-lymphocyte-associated protein 4, which was presumed to be a costimulatory molecule on activated T cells, turned out to be critical in downregulating immunity. These results, coupled with the vast suppressor cell literature which had been largely rebuked, suggested that the immune system was not poised for response but controlled in such a way that regulation was dominant. Over the last decade, we have learned that these costimulatory molecules play a key role in the now classical CD4(+)CD25(+)Foxp3(+) regulatory T cells (Tregs) that provide critical control of unwanted autoimmune responses. In this review, we discuss the connections between costimulation and Tregs that have changed the costimulation paradigm.

Indexed as

AnimalsAntigens, CDB7-1 AntigenCD28 AntigensCTLA-4 AntigenForkhead Transcription FactorsHumansLymphocyte ActivationMiceSignal TransductionThymus GlandT-Lymphocytes, RegulatoryAntigens, CDB7-1 AntigenCD28 AntigensCTLA-4 AntigenCTLA4 protein, humanCtla4 protein, mouseForkhead Transcription Factors

Identifiers

PMID19426214
PMCPMC2714548
OpenAlexW2055264495

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.