Evidence map›Paper›PMID 19801511›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Cutting Edge: Tumor-specific CD8+ T cells infiltrating prostatic tumors are induced to become suppressor cells.

Kimberly A Shafer-Weaver, Michael J Anderson, Katherine Stagliano, Anatoli Malyguine, Norman M Greenberg, Arthur A Hurwitz

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

49 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. [Research Status of Tumor-associated Fibroblasts Regulating Immune Cells].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2022
    Review
  8. Targeting the spectrum of immune checkpoints in prostate cancer.Expert review of clinical pharmacology · 2021
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. [Progress on cancer associated fibroblasts in tumor immunoregulation].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2018
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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 3 institutions in 1 country.

Kimberly A Shafer-WeaverTumor Immunity and Tolerance Section, Laboratory of Molecular Immunoregulation, Cancer and Inflammation Program, National Cancer Institute-Frederick, Frederick, MD 21702, USA.
Michael J Anderson
Katherine Stagliano
Anatoli Malyguine
Norman M Greenberg
Arthur A Hurwitz
Frederick National Laboratory for Cancer Research · USFred Hutch Cancer Center · USScience Applications International Corporation (United States) · US

Funding

Tumor Growth and Microenvironment Influence T Cell Tolerance to Tumor AntigensZIABC010954 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HURWITZ, ARTHUR · 2009 to 2015
$3.4M
Modulating T cell tolerance to elicit tumor immunity and autoimmunityZ01BC010563 · NCI · BASIC SCIENCES · PI HURWITZ, ARTHUR ANDREW · 2004 to 2007
$650k
Intramural NIH HHS Z01 BC010563NCI NIH HHS N01 CO012400NCI NIH HHS N01-CO-12400
6 · The paper itself

Abstract

We previously reported that naive, tumor-specific CD8(+) (TcR-I) T cells transferred into prostate tumor-bearing mice traffic to the prostate where they become tolerized. We now report that TcR-I cells suppress the proliferation of naive T cells. This suppression is mediated at least in part by secreted factors, and the suppressive activity can be blocked by Abs directed against TGF-beta. We further report that TcR-I cells must infiltrate the prostate to acquire suppressive activity. Delivery of tumor-specific CD4(+) T cells prevents the conversion of TcR-I cells into suppressor cells. Taken together, our findings may have critical implications for sustaining T cell responsiveness during immunotherapy, as the development of suppressor cells in the tumor microenvironment may eliminate the potency of T cells primed in the periphery or delivered during adoptive immunotherapy.

Indexed as

AnimalsAntibodiesCD8-Positive T-LymphocytesImmune ToleranceImmunotherapy, AdoptiveLymphocytes, Tumor-InfiltratingMaleMiceMice, TransgenicProstatic NeoplasmsT-Lymphocytes, RegulatoryTransforming Growth Factor betaAntibodiesTransforming Growth Factor beta

Identifiers

PMID19801511
PMCPMC6948842
OpenAlexW2162204705

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.