Evidence map›Paper›PMID 18836718›Full record

ArticleCancer immunology, immunotherapy : CII2009

Characterization of MHC class-I restricted TCRalphabeta+ CD4- CD8- double negative T cells recognizing the gp100 antigen from a melanoma patient after gp100 vaccination.

Simon Voelkl, Tamson V Moore, Michael Rehli, Michael I Nishimura, Andreas Mackensen, Karin Fischer

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

27 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. SLAMF7 promotes TCRαβJournal of experimental & clinical cancer research : CR · 2025
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  16. Reparative T lymphocytes in organ injury.The Journal of clinical investigation · 2019
    Review
  17. Article
  18. 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

6 authors at 4 institutions in 2 countries.

Simon VoelklDepartment of Internal Medicine 5, Hematology/Oncology, University of Erlangen-Nuernberg, Krankenhausstrasse 12, Erlangen, Germany.
Tamson V Moore
Michael Rehli
Michael I Nishimura
Andreas Mackensen
Karin Fischer
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversity of Regensburg · DEMedical University of South Carolina · USUniversity of Chicago · US

Funding

TCR Affinity and Therapeutic Efficacy of T CellsR01CA104947 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI NISHIMURA, MICHAEL I. · 2007 to 2011
$1.9M
Animal Model for Her-2/neu Specific TCR Gene TransferR01CA102280 · NCI · UNIVERSITY OF CHICAGO · PI NISHIMURA, MICHAEL I · 2003 to 2007
$1.4M
Tumor Recognition by TCR Transduced CD4+ and CD8+T CellsR01CA090873 · NCI · UNIVERSITY OF CHICAGO · PI NISHIMURA, MICHAEL I · 2001 to 2004
$1.3M
NCI NIH HHS CA 102280NCI NIH HHS CA 104947NCI NIH HHS CA 90873NCI NIH HHS R01 CA090873NCI NIH HHS R01 CA102280NCI NIH HHS R01 CA104947
6 · The paper itself

Abstract

The immune attack against malignant tumors require the concerted action of CD8+ cytotoxic T lymphocytes (CTL) as well as CD4+ T helper cells. The contribution of T cell receptor (TCR) alphabeta+ CD4- CD8- double-negative (DN) T cells to anti-tumor immune responses is widely unknown. In previous studies, we have demonstrated that DN T cells with a broad TCR repertoire are present in humans in the peripheral blood and the lymph nodes of healthy individuals. Here, we characterize a human DN T cell clone (T4H2) recognizing an HLA-A2-restricted melanoma-associated antigenic gp100-peptide isolated from the peripheral blood of a melanoma patient. Antigen recognition by the T4H2 DN clone resulted in specific secretion of IFN-gamma and TNF. Although lacking the CD8 molecule the gp100-specific DN T cell clone was able to confer antigen-specific cytotoxicity against gp100-loaded target cells as well as HLA-A2+ gp100 expressing melanoma cells. The cytotoxic capacity was found to be perforin/granzymeB-dependent. Together, these data indicate that functionally active antigen-specific DN T cells recognizing MHC class I-restricted tumor-associated antigen (TAA) may contribute to anti-tumor immunity in vivo.

Indexed as

Immunotherapy, ActiveAntigen PresentationAntigens, CDAntigens, NeoplasmCancer VaccinesCell Line, TumorClone CellsCytotoxicity, Immunologicgp100 Melanoma AntigenGranzymesHLA-A2 AntigenHumansImmunophenotypingInterferon-gammaInterleukinsMelanomaAntigens, CDAntigens, NeoplasmCancer Vaccinesgp100 Melanoma AntigenGranzymesHLA-A2 AntigenInterferon-gammaInterleukinsMembrane GlycoproteinsPerforinPMEL protein, humanReceptors, Antigen, T-Cell, alpha-betaTumor Necrosis Factor-alpha

Identifiers

PMID18836718
PMCPMC2832593
OpenAlexW2052637359

What OpenQuestion holds

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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.