Evidence map›Paper›PMID 25837513›Full record

Trial reportScience (New York, N.Y.)2015

Cancer immunotherapy. A dendritic cell vaccine increases the breadth and diversity of melanoma neoantigen-specific T cells.

Beatriz M Carreno, Vincent Magrini, Michelle Becker-Hapak, Saghar Kaabinejadian, Jasreet Hundal, Allegra A Petti, Amy Ly, Wen-Rong Lie, William H Hildebrand, Elaine R Mardis and 1 more

3 registry-linked trialsOpen access · greenAbstract readClinical Trial, Phase III
In one paragraph

Trial report in Science (New York, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 801 papers.

0numbers the graph read from it
0cells of the map it votes in
801citing papers in PubMed
52.7field-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.

NCT02959905 phase1completednot on this mapstarted 2016, after this paper: background citation

Phase I Clinical Trial of TSA-CTL (Tumor Specific Antigen-Induced Cytotoxic T Lymphocytes) In the Treatment of Advanced Solid Tumors

TypeinterventionalSponsorBGI, ChinaRan2016 to 2022Enrolled11ConditionsSolid CancerArmsTSA-CTL, Cyclophosphamide, Fludarabine
NCT03185429 naunknown statusnot on this mapstarted 2017, after this paper: background citation

Study of DC Vaccine Loaded Tumor Specific Antigen in Treating Patients With Gastrointestinal Solid Tumor

TypeinterventionalSponsorBGI, ChinaRan2017 to 2019Enrolled20ConditionsTumor Gastric, Tumor, ColorectalArmsTumor Specific Antigen-loaded Dendritic Cells, Cyclophosphamide
NCT05270720 phase1unknown statusnot on this mapstarted 2022, after this paper: background citation

Dendritic Cell Vaccination for the Adult Ovarian Cancer

TypeinterventionalSponsorWest China Second University HospitalRan2022 to 2024Enrolled9ConditionsRecurrent Ovarian CancerArmsdendritic cell
3 · Its place in the literature

Who cites it

801 citing papers in PubMed, 1,271 citations in OpenAlex.

  1. Review
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  10. Automating neoantigen selection for personalized cancer vaccine design.medRxiv : the preprint server for health sciences · 2026
    Article
  11. Article
  12. Cellular immunotherapy in melanoma: the next frontier in cancer treatment.Journal of experimental & clinical cancer research : CR · 2026
    Review
  13. Review
  14. Review
  15. Article
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  18. Review
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741 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Beatriz M CarrenoDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA. bcarreno@dom.wustl.edu.
Vincent MagriniGenome Institute, Washington University School of Medicine, St. Louis, MO, USA.
Michelle Becker-HapakDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Saghar KaabinejadianDepartment of Microbiology and Immunology, University of Oklahoma Health Science Center, Oklahoma City, OK, USA.
Jasreet HundalGenome Institute, Washington University School of Medicine, St. Louis, MO, USA.
Allegra A PettiGenome Institute, Washington University School of Medicine, St. Louis, MO, USA.
Amy LyGenome Institute, Washington University School of Medicine, St. Louis, MO, USA.
Wen-Rong LieEMD Millipore Corporation, Billerica, MA, USA.
William H HildebrandDepartment of Microbiology and Immunology, University of Oklahoma Health Science Center, Oklahoma City, OK, USA.
Elaine R MardisGenome Institute, Washington University School of Medicine, St. Louis, MO, USA.
Gerald P LinetteDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Washington University in St. Louis · USUniversity of Oklahoma Health Sciences Center · US

Funding

Large Scale Genome SequencingU54HG003079 · NHGRI · WASHINGTON UNIVERSITY · PI DUTCHER, SUSAN K · 2004 to 2016
$445.7M
Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
SOMATIC NON-SYNONYMOUS MUTATIONS AS UNIQUE TUMOR ANTIGENS IN MELANOMAR21CA179695 · NCI · WASHINGTON UNIVERSITY · PI CARRENO, BEATRIZ M. · 2013 to 2014
$359k
AFFINITY PURIFICATION OF LARGE FRAGMENTS OF HUMAN DNAR01HG000307 · NHGRI · YALE UNIVERSITY · PI WARD, DAVID C · 1990 to 1992
–
NCI NIH HHS P30 CA091842NCI NIH HHS P30 CA91842NCI NIH HHS R21 CA179695NHGRI NIH HHS 5U54HG00307NHGRI NIH HHS U54 HG003079
6 · The paper itself

Abstract

T cell immunity directed against tumor-encoded amino acid substitutions occurs in some melanoma patients. This implicates missense mutations as a source of patient-specific neoantigens. However, a systematic evaluation of these putative neoantigens as targets of antitumor immunity is lacking. Moreover, it remains unknown whether vaccination can augment such responses. We found that a dendritic cell vaccine led to an increase in naturally occurring neoantigen-specific immunity and revealed previously undetected human leukocyte antigen (HLA) class I-restricted neoantigens in patients with advanced melanoma. The presentation of neoantigens by HLA-A*02:01 in human melanoma was confirmed by mass spectrometry. Vaccination promoted a diverse neoantigen-specific T cell receptor (TCR) repertoire in terms of both TCR-β usage and clonal composition. Our results demonstrate that vaccination directed at tumor-encoded amino acid substitutions broadens the antigenic breadth and clonal diversity of antitumor immunity.

Indexed as

Amino Acid SubstitutionAntigen PresentationAntigens, NeoplasmCancer VaccinesDendritic CellsHLA-A2 AntigenHumansImmunotherapy, ActiveMelanomaMonitoring, ImmunologicMutationReceptors, Antigen, T-Cell, alpha-betaSkin NeoplasmsT-LymphocytesAntigens, NeoplasmCancer VaccinesHLA-A*02:01 antigenHLA-A2 AntigenReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID25837513
PMCPMC4549796
OpenAlexW2007026865

What OpenQuestion holds

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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.