Evidence map›Paper›PMID 24377099›Full record

Trial reportCancer immunology research2013

Peptide vaccination in Montanide adjuvant induces and GM-CSF increases CXCR3 and cutaneous lymphocyte antigen expression by tumor antigen-specific CD8 T cells.

Eleanor Clancy-Thompson, Laura K King, Lenora D Nunnley, Irene M Mullins, Craig L Slingluff, David W Mullins

Open access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Cancer immunology research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

25 citing papers in PubMed, 31 citations in OpenAlex.

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  14. Th17 cells inhibit CD8Journal of hematology & oncology · 2020
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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 1 institution in 1 country.

Eleanor Clancy-ThompsonDepartment of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756 ; Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756.
Laura K KingDepartment of Microbiology, Immunology, and Cancer Biology, University of Virginia School of Medicine, Charlottesville, VA 22908.
Lenora D NunnleyDepartment of Microbiology, Immunology, and Cancer Biology, University of Virginia School of Medicine, Charlottesville, VA 22908.
Irene M MullinsDepartment of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756.
Craig L SlingluffDepartment of Surgery, University of Virginia School of Medicine, Charlottesville, VA 22908.
David W MullinsDepartment of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756 ; Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756.
University of Virginia · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
Cancer Research Training Program: From Molecular Mechanisms to Therapeutic StrategiesT32CA009109 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Andrew Carl Dudley, Melanie R Rutkowski · 1985 to 2026
$13.9M
IMMUNOBIOLOGY OF MYELOID AND LYMPHOID CELLST32AI007363 · NIAID · DARTMOUTH COLLEGE · PI Claudia V Jakubzick · 1990 to 2026
$9.5M
Role of CXCR3 for CD8+ T cells in cancer immunotherapyR01CA134799 · NCI · UNIVERSITY OF VIRGINIA · PI MULLINS, DAVID W. · 2009 to 2013
$1.6M
MULTI-EPITOPE MELANOMA PEPTIDE VACCINATION WITH GM-CSFR21CA103528 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI SLINGLUFF, CRAIG LEE · 2003 to 2004
$676k
NCI NIH HHS P30 CA023108NCI NIH HHS R01 CA134799NCI NIH HHS R21 CA103528NCI NIH HHS T32 CA009109NCI NIH HHS USPHS T32 CA009109NIAID NIH HHS T32 AI007363NIAID NIH HHS USPHS T32 AI007363
6 · The paper itself

Abstract

T cell infiltration of melanoma is associated with enhanced clinical efficacy and is a desirable endpoint of immunotherapeutic vaccination. Infiltration is regulated, in part, by chemokine receptors and selectin ligands on the surface of tumor-specific lymphocytes. Therefore, we investigated the expression of two homing molecules--CXCR3 and CLA - on vaccine-induced CD8 T cells, in the context of a clinical trial of a melanoma-specific peptide vaccine. Both CXCR3 and CLA have been associated with T cell infiltration of melanoma. We demonstrate that a single subcutaneous/intradermal administration of peptide vaccine in Montanide adjuvant induces tumor-specific CD8 T cells that are predominantly positive for CXCR3, with a subpopulation of CXCR3(+)CLA(+) cells. Addition of GM-CSF significantly enhances CXCR3 expression and increases the proportion of CLA-expressing cells. Concurrent with CXCR3 and CLA expression, vaccine-induced CD8 cells express high levels of Tbet, IFN-γ, and IL-12Rβ1. Collectively, these studies demonstrate that peptide vaccination in adjuvant induces CD8 T cells with a phenotype that may support infiltration of melanoma.

Indexed as

Amino Acid SequenceAntigens, NeoplasmCancer VaccinesCD8-Positive T-LymphocytesGranulocyte-Macrophage Colony-Stimulating FactorHumansMannitolMelanomaMolecular Sequence DataNeoplasm ProteinsOleic AcidsPeptidesReceptors, CXCR3Antigens, NeoplasmCancer VaccinesCXCR3 protein, humanGranulocyte-Macrophage Colony-Stimulating FactorMannitolmontanide ISA 51Neoplasm ProteinsOleic AcidsPeptidesReceptors, CXCR3adjuvantCLACXCR3GM-CSFIL-12Rmelanomapeptide vaccines

Identifiers

PMID24377099
PMCPMC3873151
OpenAlexW2124935667

What OpenQuestion holds

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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.