Evidence map›Paper›PMID 17346430›Full record

ArticleInternational journal of immunopathology and pharmacology

HLA-A2.1-restricted T cells react to SEREX-defined tumor antigen CML66L and are suppressed by CD4+CD25+ regulatory T cells.

Y Yan, Y Chen, F Yang, I H Chen, Z Xiong, J Wang, L B Lachman, H Wang, X-F Yang

Open access · greenAbstract read
In one paragraph

Article in International journal of immunopathology and pharmacology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Higher expression of Bax in regulatory T cells increases vascular inflammation.Frontiers in bioscience : a journal and virtual library · 2008
    Article
  12. Article
  13. Article
  14. Article
  15. Inflammasomes are differentially expressed in cardiovascular and other tissues.International journal of immunopathology and pharmacology
    Article
  16. CD25high T cells with a prolonged survival inhibit development of diabetes.International journal of immunopathology and pharmacology
    Article
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

9 authors at 2 institutions in 1 country.

Y YanDepartment of Pharmacology, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Y Chen
F Yang
I H Chen
Z Xiong
J Wang
L B Lachman
H Wang
X-F Yang
Temple University · USThe University of Texas MD Anderson Cancer Center · US

Funding

Survival of CD4+CD25+ Regulatory T CellsK08AI054514 · NIAID · TEMPLE UNIV OF THE COMMONWEALTH · PI YANG, XIAO-FENG · 2003 to 2007
$589k
NIAID NIH HHS AI054514NIAID NIH HHS K08 AI054514
6 · The paper itself

Abstract

The question of whether T cell responses to SEREX-defined tumor antigens are under regulation of naturally occurring CD4+CD25+ regulatory T cells (nTreg cells) has not been answered. To address this issue, we first identified an HLA-A2.1-restricted T cell antigen epitope of SEREX-identified tumor antigen CML66L, 66Pa. The HLA-A2.1/66Pa peptide complex in vitro stimulated the in vivo-primed T cells as shown by increased T cell proliferation, higher secretion of the T cell cytokine interferon-gamma (IFN-gamma), increased production of intracellular IFN-gamma in CD8+ T cells, and higher T cell-mediated cytotoxicities of CML66L+ human tumor cells. This suggests that CML66L elicits T cell immune responses. We also developed a novel internal reference epitope for identification of T cell epitopes by construction of chimeric CML66L containing myeloid antigen proteinase 3 epitope Pr1 as a control. Finally, we found that nTreg cells regulates T cell responses to 66Pa, and that depletion of nTreg cells via a pro-apoptotic protein Bax-dependent mechanism enhances polyclonal T cell responses to 66Pa. These findings provide new insights into the T cell participation in SEREX-defined anti-tumor immune responses and novel direction in enhancement of anti-leukemia immunotherapy by modulation of homeostasis of nTreg cells.

Indexed as

AnimalsAntigensAntigens, NeoplasmApoptosisbcl-2-Associated X ProteinCD4-Positive T-LymphocytesCell LineCloning, MolecularEpitopesHeLa CellsHLA-A2 AntigenHomeostasisHumansImmunoglobulin GInterferon-gammaInterleukin-2 Receptor alpha SubunitAntigensAntigens, Neoplasmbcl-2-Associated X ProteinEpitopesHLA-A2 AntigenImmunoglobulin GInterferon-gammaInterleukin-2 Receptor alpha SubunitNUDCD1 protein, humanPeptidesVaccines, DNA

Identifiers

PMID17346430
PMCPMC2919235
OpenAlexW2223896800

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.