Evidence map›Paper›PMID 19662679›Full record

ArticleThe Journal of clinical investigation2009

Identification of heme oxygenase-1-specific regulatory CD8+ T cells in cancer patients.

Mads Hald Andersen, Rikke Baek Sørensen, Marie K Brimnes, Inge Marie Svane, Jürgen C Becker, Per thor Straten

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

38 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
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  3. Article
  4. Review
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  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Immune Modulation by Inhibitors of the HO System.International journal of molecular sciences · 2020
    Review
  12. Article
  13. Article
  14. Heme oxygenase inhibition in cancers: possible tools and targets.Contemporary oncology (Poznan, Poland) · 2018
    Review
  15. Anti-regulatory T cells.Seminars in immunopathology · 2017
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Heme oxygenase-1: emerging target of cancer therapy.Journal of biomedical science · 2015
    Review
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 2 institutions in 2 countries.

Mads Hald AndersenCenter for Cancer Immune Therapy, Department of Hematology, Herlev University Hospital, Herlev, Denmark. mahaan01@heh.regionh.dk
Rikke Baek Sørensen
Marie K Brimnes
Inge Marie Svane
Jürgen C Becker
Per thor Straten
Herlev Hospital · DKUniversity of Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treg deficiencies are associated with autoimmunity. Conversely, CD4+ and CD8+ Tregs accumulate in the tumor microenvironment and are associated with prevention of antitumor immunity and anticancer immunotherapy. Recently, CD4+ Tregs have been much studied, but little is known about CD8+ Tregs and the antigens they recognize. Here, we describe what we believe to be the first natural target for CD8+ Tregs. Naturally occurring HLA-A2-restricted CD8+ T cells specific for the antiinflammatory molecule heme oxygenase-1 (HO-1) were able to suppress cellular immune responses with outstanding efficacy. HO-1-specific CD8+ T cells were detected ex vivo and in situ among T cells from cancer patients. HO-1-specific T cells isolated from the peripheral blood of cancer patients inhibited cytokine release, proliferation, and cytotoxicity of other immune cells. Notably, the inhibitory effect of HO-1-specific T cells was far more pronounced than that of conventional CD4+CD25+CD127- Tregs. The inhibitory activity of HO-1-specific T cells seemed at least partly to be mediated by soluble factors. Our data link the cellular stress response to the regulation of adaptive immunity, expand the role of HO-1 in T cell-mediated immunoregulation, and establish a role for peptide-specific CD8+ T cells in regulating cellular immune responses. Identification of potent antigen-specific CD8+ Tregs may open new avenues for therapeutic interventions in both autoimmune diseases and cancer.

Indexed as

CD8-Positive T-LymphocytesHeme Oxygenase-1HLA-A2 AntigenHumansImmunophenotypingInterferon-gammaInterleukin-10Lymphocyte ActivationNeoplasmsT-Lymphocytes, RegulatoryHeme Oxygenase-1HLA-A2 AntigenInterferon-gammaInterleukin-10

Identifiers

PMID19662679
PMCPMC2719937
OpenAlexW1999569754

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.