Evidence map›Paper›PMID 15753211›Full record

ArticleThe Journal of experimental medicine2005

Intratumor depletion of CD4+ cells unmasks tumor immunogenicity leading to the rejection of late-stage tumors.

Ping Yu, Youjin Lee, Wenhua Liu, Thomas Krausz, Anita Chong, Hans Schreiber, Yang-Xin Fu

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 173 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
173citing papers in PubMed, 1 pooled it
16.2field-weighted citation impact, top 1% 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

173 citing papers in PubMed, 1 synthesis or guideline pooled it, 425 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. CD4Oncoimmunology · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Depletion of conventional CD4Journal for immunotherapy of cancer · 2024
    Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review

113 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

7 authors at 1 institution in 1 country.

Ping YuThe Committee on Immunology, University of Chicago, Chicago, IL 60637, USA. pingyu@uchicago.edu
Youjin Lee
Wenhua Liu
Thomas Krausz
Anita Chong
Hans Schreiber
Yang-Xin Fu
University of Chicago · US

Funding

Research Training in Digestive Health, Diseases, and NutritionT32DK007074 · NIDDK · UNIVERSITY OF CHICAGO · PI EUGENE B CHANG · 1986 to 2026
$11.3M
PATHOBIOLOGY OF MYELOMA AND ANTI-IDIOTYPIC IMMUNITYR01CA022677 · NCI · UNIVERSITY OF CHICAGO · PI SCHREIBER, HANS · 1985 to 2024
$6.3M
IMMUNOLOGY OF UNIQUE TUMOR-SPECIFIC ANTIGENSR01CA037156 · NCI · UNIVERSITY OF CHICAGO · PI SCHREIBER, HANS · 1985 to 2017
$3.1M
THE ROLE OF LYMPHOID MICROENVIRONMENT IN AUTOIMMUNITYR01DK058897 · NIDDK · UNIVERSITY OF CHICAGO · PI FU, YANG-XIN · 2001 to 2009
$2.9M
DEVELOPMENT AND FUNCTION OF LYMPHOID TISSUESR01HD037104 · NICHD · UNIVERSITY OF CHICAGO · PI FU, YANG-XIN · 1999 to 2003
$491k
NCI NIH HHS P01-CA09296-01NCI NIH HHS R01 CA022677NCI NIH HHS R01 CA037156NCI NIH HHS R01-CA22677NCI NIH HHS R01-CA37156NICHD NIH HHS R01 HD037104NICHD NIH HHS R01-HD37104NIDDK NIH HHS 5T32DK07074NIDDK NIH HHS R01 DK058897NIDDK NIH HHS R01-DK58897NIDDK NIH HHS T32 DK007074
6 · The paper itself

Abstract

Tumor environment can be critical for preventing the immunological destruction of antigenic tumors. We have observed a selective accumulation of CD4(+)CD25(+) T cells inside tumors. In a murine fibrosarcoma L(d)-expressing Ag104, these cells made up the majority of tumor-infiltrating lymphocytes at the late stage of tumor progression, and their depletion during the effector phase, rather than priming phase, successfully enhanced antitumor immunity. We show here that CD4(+)CD25(+) T cells suppressed the proliferation and interferon-gamma production of CD8(+) T cells in vivo at the local tumor site. Blockade of the effects of IL-10 and TGF-beta partially reversed the suppression imposed by the CD4(+) cells. Furthermore, local depletion of CD4(+) cells inside the tumor resulted in a change of cytokine milieu and led to the eradication of well-established highly aggressive tumors and the development of long-term antitumor memory. Therefore, CD4(+)CD25(+) T cells maintained an environment in the tumor that concealed the immunogenicity of tumor cells to permit progressive growth of antigenic tumors. Our study illustrates that the suppression of antitumor immunity by regulatory T cells occurs predominantly at the tumor site, and that local reversal of suppression, even at a late stage of tumor development, can be an effective treatment for well-established cancers.

Indexed as

Adoptive TransferAnimalsAntigens, NeoplasmCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell ProliferationCells, CulturedImmune ToleranceInterferon-gammaInterleukin-10MaleMiceNeoplasmsNeoplasm StagingReceptors, Interleukin-2Transforming Growth Factor betaAntigens, NeoplasmInterferon-gammaInterleukin-10Receptors, Interleukin-2Transforming Growth Factor beta

Identifiers

PMID15753211
PMCPMC2212829
OpenAlexW2132207502

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.