Evidence map›Paper›PMID 23319803›Full record

ArticleCancer research2013

Delicate balance among three types of T cells in concurrent regulation of tumor immunity.

Liat Izhak, Elena Ambrosino, Shingo Kato, Stanley T Parish, Jessica J O'Konek, Hannah Weber, Zheng Xia, David Venzon, Jay A Berzofsky, Masaki Terabe

Abstract read
In one paragraph

Article in Cancer research, 2013. 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
3.8field-weighted citation impact, top 6% 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, 52 citations in OpenAlex.

  1. CD8Evidence-based complementary and alternative medicine : eCAM · 2023
    Article
  2. Review
  3. Japanese Kampo Medicine Juzentaihoto Improves Antiviral Cellular Immunity in Tumour-Bearing Hosts.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Innate T cells in the intensive care unit.Molecular immunology · 2019
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Tumor-infiltrating CD4Cancer cell international · 2017
    Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. 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

10 authors at 2 institutions in 1 country.

Liat IzhakVaccine Branch and Biostatistics and Data Management Section, Center for Cancer Research, National Cancer Institute/NIH, Bethesda, MD 20892, USA.
Elena Ambrosino
Shingo Kato
Stanley T Parish
Jessica J O'Konek
Hannah Weber
Zheng Xia
David Venzon
Jay A Berzofsky
Masaki Terabe
Center for Cancer Research · USNational Cancer Institute · US

Funding

Vaccine and immunotherapy strategies for cancer and viruses causing cancerZIASC004020 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI BERZOFSKY, JAY A · 2009 to 2025
$51.8M
Office of Collaborative BiostatisticsZIDSC007202 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI CHOO-WOSOBA, HYOYOUNG · 2009 to 2025
$14.5M
Intramural NIH HHS Z99 CA999999NCI NIH HHS Y99 CA999999
6 · The paper itself

Abstract

The nature of the regulatory cell types that dominate in any given tumor is not understood at present. Here, we addressed this question for regulatory T cells (Treg) and type II natural killer T (NKT) cells in syngeneic models of colorectal and renal cancer. In mice with both type I and II NKT cells, or in mice with neither type of NKT cell, Treg depletion was sufficient to protect against tumor outgrowth. Surprisingly, in mice lacking only type I NKT cells, Treg blockade was insufficient for protection. Thus, we hypothesized that type II NKT cells may be neutralized by type I NKT cells, leaving Tregs as the primary suppressor, whereas in mice lacking type I NKT cells, unopposed type II NKT cells could suppress tumor immunity even when Tregs were blocked. We confirmed this hypothesis in 3 ways by reconstituting type I NKT cells as well as selectively blocking or activating type II NKT cells with antibody or the agonist sulfatide, respectively. In this manner, we showed that blockade of both type II NKT cells and Tregs is necessary to abrogate suppression of tumor immunity, but a third cell, the type I NKT cell, determines the balance between these regulatory mechanisms. As patients with cancer often have deficient type I NKT cell function, managing this delicate balance among 3 T-cell subsets may be critical for the success of immunotherapy for human cancer.

Indexed as

AnimalsCell Line, TumorColorectal NeoplasmsFemaleKidney NeoplasmsMiceMice, Inbred BALB CNatural Killer T-CellsSulfoglycosphingolipidsT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsSulfoglycosphingolipids

Identifiers

PMID23319803
PMCPMC3622595
OpenAlexW2151401991

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.