Evidence map›Paper›PMID 19188167›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2009

B7 blockade alters the balance between regulatory T cells and tumor-reactive T cells for immunotherapy of cancer.

Penghui Zhou, Xincheng Zheng, Huiming Zhang, Yang Liu, Pan Zheng

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. GPCR Biased Signaling in Cancer.Handbook of experimental pharmacology · 2026
    Review
  2. Article
  3. Article
  4. GPCRs: emerging targets for novel T cell immune checkpoint therapy.Cancer immunology, immunotherapy : CII · 2024
    Review
  5. The role of regulatory T cells in vitiligo and therapeutic advances: a mini-review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. 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

5 authors at 2 institutions in 1 country.

Penghui ZhouDepartment of Surgery and Pathology, University of Michigan Medical Center, Program of Molecular Mechanism of Diseases and Comprehensive Cancer Center, Ann Arbor, Michigan 48109, USA.
Xincheng Zheng
Huiming Zhang
Yang Liu
Pan Zheng
University of Michigan–Ann Arbor · USOncoImmune (United States) · US

Funding

Checkpoints of Host Response to Cellular InjuriesR01AI064350 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, YANG, ZHENG, PAN · 2006 to 2019
$5.6M
Selective Modulation of Cancer Immunity and AutoimmunityR01CA112001 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, YANG · 2006 to 2010
$1.3M
NCI NIH HHS CA12001NCI NIH HHS R01 CA112001NIAID NIH HHS AI064350NIAID NIH HHS R01 AI064350
6 · The paper itself

Abstract

purposeIn prostate cancer-bearing host, regulatory T (Treg) cells restrain activity of tumor antigen-specific T cells. Because B7:CD28 interactions are needed for both function of CD4+CD25+ Treg cells and CD8+ effective T cells, targeting this pathway may help to overcome the immunotherapy barriers. EXPERIMENTAL

designThe anti-B7-1/B7-2 monoclonal antibodies were administered to a transgenic mouse model of prostate cancer (TRAMP) ectopically expressing SV40 large T antigen in different tumor development stages for prevention and therapy of prostate cancer. The treatment was also tested in treating transplanted MC38 colon adenocarcinoma in mice.

resultsHere, we showed that short-term administration of anti-B7-1/B7-2 monoclonal antibodies in TRAMP mice leads to significant inhibited primary tumor growth and the size of metastatic lesions. The treatment is effective to inhibit MC38 colon cancer growth. Correspondingly, this treatment results in a transient reduction of Treg in both thymus and the periphery. In vivo cytotoxicity assay revealed T antigen-specific CTL effectors in anti-B7-treated but not control IgG-treated TRAMP mice.

conclusionsTransient blockade of B7-1/B7-2 alters the balance between Treg and cancer-reactive T cells to enhance cancer immunotherapy.

Indexed as

AnimalsAntibodies, Anti-IdiotypicAntibodies, MonoclonalB7-1 AntigenB7-2 AntigenDisease Models, AnimalImmunotherapyInterleukin-2 Receptor alpha SubunitLymphocyte ActivationMaleMiceMice, Inbred C57BLMice, TransgenicProstatic NeoplasmsT-Lymphocytes, CytotoxicT-Lymphocytes, Regulatory107-1A4 monoclonal antibodyAntibodies, Anti-IdiotypicAntibodies, MonoclonalB7-1 AntigenB7-2 AntigenInterleukin-2 Receptor alpha Subunit

Identifiers

PMID19188167
PMCPMC2693886
OpenAlexW2125126023

What OpenQuestion holds

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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.