Evidence map›Paper›PMID 16819631›Full record

ReviewCancer immunology, immunotherapy : CII2007

CD4 regulatory T cells in human cancer pathogenesis.

Keith L Knutson, Mary L Disis, Lupe G Salazar

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00726037 (A Pilot Study Evaluating the Efficacy of Regulatory T-cell), which is not on this map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
3.7field-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.

NCT00726037 phase2terminatednot on this mapstarted 2008, after this paper: background citation

A Pilot Study Evaluating the Efficacy of Regulatory T-cell (T-reg) Suppression by Denileukin Diftitox (Ontak) in Metastatic Pancreatic Cancer

TypeinterventionalSponsorLoyola UniversityRan2008 to 2012Enrolled7ConditionsMetastatic Pancreatic CancerArmsOntak
3 · Its place in the literature

Who cites it

61 citing papers in PubMed, 114 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Immune mediated support of metastasis: Implication for bone invasion.Cancer communications (London, England) · 2024
    Review
  9. Review
  10. Immune checkpoint analysis in ear cancer.Head & face medicine · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Immunological Prognostic Factors in Multiple Myeloma.International journal of molecular sciences · 2021
    Review
  16. T-Regulatory Cells In Tumor Progression And Therapy.Cancer management and research · 2019
    Review
  17. Melatonin and Hippo Pathway: Is There Existing Cross-Talk?International journal of molecular sciences · 2017
    Article
  18. Review
  19. Review
  20. Article

1 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

3 authors at 1 institution in 1 country.

Keith L KnutsonDepartment of Immunology, Mayo Clinic College of Medicine, Mayo Clinic, 342C Guggenheim, 200 First Street SW, Rochester, MN 55905, USA. knutson.keith@mayo.edu
Mary L Disis
Lupe G Salazar
Mayo Clinic in Florida · US

Funding

HLA classl complex expression in breast cancer immunityR01CA113861 · NCI · MAYO CLINIC ROCHESTER · PI KNUTSON, KEITH L. · 2005 to 2009
$1.1M
Ex vivo expansion of HER-2/neu specific T helper cellsK01CA100764 · NCI · UNIVERSITY OF WASHINGTON · PI KNUTSON, KEITH L. · 2004 to 2008
$742k
NCI NIH HHS K01 CA 100764NCI NIH HHS K01 CA100764NCI NIH HHS R01 CA 113861NCI NIH HHS R01 CA113861
6 · The paper itself

Abstract

Over the past decade, there has been an accelerated understanding of immune regulatory mechanisms. Peripheral immune regulation is linked to a collection of specialized regulatory cells of the CD4(+) T cell lineage (i.e., CD4(+) Tregs). This collection consists of Tregs that are either thymically derived (i.e., natural) or peripherally induced. Tregs are important for controlling potentially autoreactive immune effectors and immunity to foreign organisms and molecules. Their importance in maintaining immune homeostasis and the overall health of an organism is clear. However, Tregs may also be involved in the pathogenesis of malignancies as now compelling evidence shows that tumors induce or recruit CD4(+) Tregs to block immune priming and antitumor effectors. Efforts are underway to develop approaches that specifically inhibit the function of tumor-associated Tregs which could lead to an increased capability of the body's immune system to respond to tumors but without off-target immune-related pathologies (i.e., autoimmune disease). In this review, the biology of human CD4(+) Tregs is discussed along with their involvement in malignancies and emerging strategies to block their function.

Indexed as

AnimalsCD4-Positive T-LymphocytesHumansNeoplasmsT-Lymphocytes, Regulatory

Identifiers

PMID16819631
PMCPMC11030088
OpenAlexW2010748775

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.