Evidence map›Paper›PMID 19285848›Full record

ReviewCurrent opinion in immunology2009

Adoptive immunotherapy of cancer using CD4(+) T cells.

Pawel Muranski, Nicholas P Restifo

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 127 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
127citing papers in PubMed, 1 pooled it
12.8field-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

127 citing papers in PubMed, 1 synthesis or guideline pooled it, 215 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Dendritic cells loaded with mRNA encoding full-length tumor antigens prime CD4+ and CD8+ T cells in melanoma patients.Molecular therapy : the journal of the American Society of Gene Therapy · 2012
    Trial
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Specific recognition of anJournal for immunotherapy of cancer · 2023
    Article
  13. Review
  14. Article
  15. The role of CD4 T cells in rejection of solid tumors.Current opinion in immunology · 2022
    Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. CD4Frontiers in oncology · 2021
    Article

67 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

2 authors at 2 institutions in 1 country.

Pawel MuranskiNational Cancer Institute, NIH, Bethesda, MD 20892, USA. muranskp@mail.nih.gov
Nicholas P Restifo
National Cancer Institute · USNational Institutes of Health · US

Funding

Building on the success of the adoptive immunotherapy of cancerZIABC010763 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ROSENBERG, STEVEN · 2009 to 2020
$25.0M
Building on the success of the adoptive immunotherapy of cancerZ01BC010763 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RESTIFO, NICHOLAS P · 2006 to 2008
$6.4M
Developing new immunotherapies based of CD4+ T cellsZIABC011037 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RESTIFO, NICHOLAS · 2009 to 2014
$4.4M
Intramural NIH HHS Z01 BC010763
6 · The paper itself

Abstract

CD4(+) T cells are central to the function of the immune system but their role in tumor immunity remains underappreciated. It is becoming clear that there is an enormous diversity of CD4(+) T cell polarization patterns including Th1, Th2, Th17, and regulatory T cells (Tregs). These functionally divergent T cell subsets can have opposing effects -- they can trigger tumor rejection or inhibit treatment after adoptive cell transfer. Some polarized CD4(+) cells have plasticity, and their phenotypes and functions can evolve in vivo. Recent advances in understanding of polarization and differentiation of lymphocytes, as well as some intriguing developments in the clinic, indicate that the use of CD4(+) T cell subsets in the immunotherapy of cancer has unrealized potential.

Indexed as

AnimalsApoptosisAutophagyCD4-Positive T-LymphocytesHumansImmunotherapy, AdoptiveModels, ImmunologicalNeoplasmsT-Lymphocytes, Helper-InducerT-Lymphocytes, Regulatory

Identifiers

PMID19285848
PMCPMC2715842
OpenAlexW2067963142

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.