Evidence map›Paper›PMID 26447332›Full record

ArticleScientific reports2015

Direct tumor recognition by a human CD4(+) T-cell subset potently mediates tumor growth inhibition and orchestrates anti-tumor immune responses.

Junko Matsuzaki, Takemasa Tsuji, Immanuel F Luescher, Hiroshi Shiku, Junichi Mineno, Sachiko Okamoto, Lloyd J Old, Protul Shrikant, Sacha Gnjatic, Kunle Odunsi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 5% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
  2. A Pilot Study of Stereotactic Body Radiation Therapy Combined with Cytoreductive Nephrectomy for Metastatic Renal Cell Carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Trial
  3. Article
  4. Review
  5. Review
  6. Article
  7. Antimelanoma Effects ofDiseases (Basel, Switzerland) · 2024
    Article
  8. Article
  9. Article
  10. Neoadjuvant Chemotherapy Is Associated with Altered Immune Cell Infiltration and an Anti-Tumorigenic Microenvironment in Resected Pancreatic Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  11. Article
  12. Bystander CD4Oncoimmunology · 2022
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Targeting Telomerase with an HLA Class II-Restricted TCR for Cancer Immunotherapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  19. Revisiting the role of CD4Cancer gene therapy · 2021
    Review
  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 6 institutions in 3 countries.

Junko MatsuzakiCenter for Immunotherapy, Roswell Park Cancer Institute, Buffalo, NY, USA.
Takemasa TsujiCenter for Immunotherapy, Roswell Park Cancer Institute, Buffalo, NY, USA.
Immanuel F LuescherLudwig Center for Cancer Research, University of Lausanne, Epalinges, Switzerland.
Hiroshi ShikuDepartment of Immuno-Gene Therapy, Mie University Graduate School of Medicine, Tsu, Mie, Japan.
Junichi MinenoTAKARA BIO INC, Otsu, Shiga, Japan.
Sachiko OkamotoTAKARA BIO INC, Otsu, Shiga, Japan.
Lloyd J OldLudwig Institute for Cancer Research, New York Branch at Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Protul ShrikantDepartment of Immunology, Roswell Park Cancer Institute, Buffalo, NY, USA.
Sacha GnjaticLudwig Institute for Cancer Research, New York Branch at Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Kunle OdunsiCenter for Immunotherapy, Roswell Park Cancer Institute, Buffalo, NY, USA.
Roswell Park Comprehensive Cancer Center · USTakara (Japan) · JPIcahn School of Medicine at Mount Sinai · USLudwig Cancer Research · CHMemorial Sloan Kettering Cancer Center · USMie University · JP

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
RPCI-UPCI Ovarian Cancer SPOREP50CA159981 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MOYSICH, KIRSTEN B. · 2013 to 2025
$19.6M
mTOR inhibition for generating memory T cells to enhance ovarian tumor immunityR01CA158318 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI ODUNSI, KUNLE, SHRIKANT, PROTUL · 2011 to 2015
$1.7M
NCI NIH HHS 1R01CA158318-01A1NCI NIH HHS P30 CA016056NCI NIH HHS P50 CA159981NCI NIH HHS P50CA159981-01A1NCI NIH HHS R01 CA158318
6 · The paper itself

Abstract

Tumor antigen-specific CD4(+) T cells generally orchestrate and regulate immune cells to provide immune surveillance against malignancy. However, activation of antigen-specific CD4(+) T cells is restricted at local tumor sites where antigen-presenting cells (APCs) are frequently dysfunctional, which can cause rapid exhaustion of anti-tumor immune responses. Herein, we characterize anti-tumor effects of a unique human CD4(+) helper T-cell subset that directly recognizes the cytoplasmic tumor antigen, NY-ESO-1, presented by MHC class II on cancer cells. Upon direct recognition of cancer cells, tumor-recognizing CD4(+) T cells (TR-CD4) potently induced IFN-γ-dependent growth arrest in cancer cells. In addition, direct recognition of cancer cells triggers TR-CD4 to provide help to NY-ESO-1-specific CD8(+) T cells by enhancing cytotoxic activity, and improving viability and proliferation in the absence of APCs. Notably, the TR-CD4 either alone or in collaboration with CD8(+) T cells significantly inhibited tumor growth in vivo in a xenograft model. Finally, retroviral gene-engineering with T cell receptor (TCR) derived from TR-CD4 produced large numbers of functional TR-CD4. These observations provide mechanistic insights into the role of TR-CD4 in tumor immunity, and suggest that approaches to utilize TR-CD4 will augment anti-tumor immune responses for durable therapeutic efficacy in cancer patients.

Indexed as

AnimalsAntigens, NeoplasmCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorCell ProliferationCells, CulturedCell SurvivalCoculture TechniquesCytotoxicity, ImmunologicFemaleHumansInterferon-gammaJurkat CellsMembrane ProteinsMice, SCIDAntigens, NeoplasmCTAG1B protein, humanInterferon-gammaMembrane ProteinsTumor Necrosis Factor-alpha

Identifiers

PMID26447332
PMCPMC4597193
OpenAlexW2345480690

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.