Evidence map›Paper›PMID 20156973›Full record

ArticleThe Journal of experimental medicine2010

Naive tumor-specific CD4(+) T cells differentiated in vivo eradicate established melanoma.

Ying Xie, Akgül Akpinarli, Charles Maris, Edward L Hipkiss, Malcolm Lane, Eun-Kyung M Kwon, Pawel Muranski, Nicholas P Restifo, Paul Andrew Antony

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 299 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
299citing 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

299 citing papers in PubMed, 1 synthesis or guideline pooled it, 444 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Cytotoxic CD4Signal transduction and targeted therapy · 2026
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Clonally expanded effector CD4Journal for immunotherapy of cancer · 2025
    Article
  17. Review
  18. Review
  19. bioRxiv : the preprint server for biology · 2025
    Article
  20. Article

239 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

9 authors at 5 institutions in 3 countries.

Ying XieProgram in Molecular Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Akgül Akpinarli
Charles Maris
Edward L Hipkiss
Malcolm Lane
Eun-Kyung M Kwon
Pawel Muranski
Nicholas P Restifo
Paul Andrew Antony
Center of Molecular Immunology (Cuba) · CUCenter for Cancer Research · USJohns Hopkins Medicine · USNational Institute of Allergy and Infectious Diseases · USUniversity of Maryland, Baltimore · 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
The role of antigen-specific CD4+ T cells during immunity to established tumorsK22CA125200 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI ANTONY, PAUL ANDREW · 2007 to 2009
$530k
NCI NIH HHS 5K22CA125200NCI NIH HHS K22 CA125200
6 · The paper itself

Abstract

In vitro differentiated CD8(+) T cells have been the primary focus of immunotherapy of cancer with little focus on CD4(+) T cells. Immunotherapy involving in vitro differentiated T cells given after lymphodepleting regimens significantly augments antitumor immunity in animals and human patients with cancer. However, the mechanisms by which lymphopenia augments adoptive cell therapy and the means of properly differentiating T cells in vitro are still emerging. We demonstrate that naive tumor/self-specific CD4(+) T cells naturally differentiated into T helper type 1 cytotoxic T cells in vivo and caused the regression of established tumors and depigmentation in lymphopenic hosts. Therapy was independent of vaccination, exogenous cytokine support, CD8(+), B, natural killer (NK), and NKT cells. Proper activation of CD4(+) T cells in vivo was important for tumor clearance, as naive tumor-specific CD4(+) T cells could not completely treat tumor in lymphopenic common gamma chain (gamma(c))-deficient hosts. gamma(c) signaling in the tumor-bearing host was important for survival and proper differentiation of adoptively transferred tumor-specific CD4(+) T cells. Thus, these data provide a platform for designing immunotherapies that incorporate tumor/self-reactive CD4(+) T cells.

Indexed as

Adoptive TransferAnimalsCD4 AntigensCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell DifferentiationHumansImmunotherapy, AdoptiveInterferon Type IMelanomaMelanoma, ExperimentalMicePregnancy ProteinsCD4 Antigensinterferon tauInterferon Type IPregnancy Proteins

Identifiers

PMID20156973
PMCPMC2839147
OpenAlexW2138397823

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.