Evidence map›Paper›PMID 10623795›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2000

Cutting edge: CD4+ T cell control of CD8+ T cell reactivity to a model tumor antigen.

D R Surman, M E Dudley, W W Overwijk, N P Restifo

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
5.0field-weighted citation impact, top 4% 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.

NCT04212377 phase2completednot on this mapstarted 2019, after this paper: background citation

An Exploratory Study: Dendritic Cells for Immunotherapy of Metastatic Endometrial Cancer Patients

TypeinterventionalSponsorRadboud University Medical CenterRan2019 to 2021Enrolled8ConditionsEndometrial CancerArmsDendritic Cells for endometrial cancer
NCT05163080 phase2unknown statusnot on this mapstarted 2021, after this paper: background citation

Prospective Randomized Placebo-Controlled Trial of SurVaxM Plus Adjuvant Temozolomide for Newly Diagnosed Glioblastoma (SURVIVE)

TypeinterventionalSponsorMimiVax, LLCRan2021 to 2024Enrolled247ConditionsNewly Diagnosed GlioblastomaArmsSurVaxM
3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 168 citations in OpenAlex.

  1. The Impact of Targeting TRAF2 and NCK-Interacting Protein Kinase on Antitumor Effect and Tumor Immune Environment in c-MYC-High SCLC.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2026
    Article
  2. Article
  3. Review
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  6. The opposing roles of CD4Immunology · 2018
    Review
  7. CD4 and CD8 T lymphocyte interplay in controlling tumor growth.Cellular and molecular life sciences : CMLS · 2018
    Review
  8. Prognostic significance of CD4 and interleukin-22 expression in pancreatic cancer.International journal of clinical and experimental pathology · 2017
    Article
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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

4 authors at 1 institution in 1 country.

D R SurmanSurgery Branch, National Cancer Institute, Bethesda, MD 20892, USA.
M E Dudley
W W Overwijk
N P Restifo
National Cancer Institute · US

Funding

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
Intramural NIH HHS Z01 BC010763Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

Neoantigens resulting from the inherent genomic instability of tumor cells generally do not trigger immune recognition. Similarly, transfection of tumors with model Ags often fails to elicit CD8+ T cell responses or alter a tumor's growth rate or lethality. We report here that the adoptive transfer of activated Th1-type CD4+ T cells specific for a model tumor Ag results in the de novo generation of CD8+ T cells with specificity to that Ag and concomitant tumor destruction. The anti-tumor effects of the CD4+ T cells required the presence of both MHC class I and class II on host cells, as evidenced by experiments in knockout mice, suggesting that CD4+ T cells enhanced the ability of host APC to activate endogenous CD8+ T cells. These results indicate that the apparent inability of tumor cells expressing highly immunogenic epitopes to activate tumor-specific CD8+ T cells can be altered by activated CD4+ T cells.

Indexed as

Adoptive TransferAnimalsAntigens, Neoplasmbeta-GalactosidaseCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell MovementClone CellsEpitopes, T-LymphocyteHistocompatibility Antigens Class IHistocompatibility Antigens Class IILymphocyte ActivationMiceMice, Inbred C57BLModels, ImmunologicalNeoplasm TransplantationAntigens, Neoplasmbeta-GalactosidaseEpitopes, T-LymphocyteHistocompatibility Antigens Class IHistocompatibility Antigens Class II

Identifiers

PMID10623795
PMCPMC2239008
OpenAlexW2155778479

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.