Evidence map›Paper›PMID 32385144›Full record

ArticleJournal for immunotherapy of cancer2020

MHC-restricted phosphopeptide antigens: preclinical validation and first-in-humans clinical trial in participants with high-risk melanoma.

Victor H Engelhard, Rebecca C Obeng, Kara L Cummings, Gina R Petroni, Angela L Ambakhutwala, Kimberly A Chianese-Bullock, Kelly T Smith, Amanda Lulu, Nikole Varhegyi, Mark E Smolkin and 11 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01846143 (Evaluation of the Safety and Immunogenicity of a Multi-phosphopeptide Vaccine Plus PolyICLC in Participants With High Risk and Advanced Malignancies), which is not on this map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
3.9field-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.

NCT01846143 phase1completednot on this map

Evaluation of the Safety and Immunogenicity of a Multi-phosphopeptide Vaccine Plus PolyICLC in Participants With High Risk and Advanced Malignancies (Mel59)

TypeinterventionalSponsorCraig L Slingluff, JrRan2013 to 2015Enrolled15ConditionsMelanomaArmspBCAR3-phosphopeptide, pIRS2-phosphopeptide, 2-MpP (pBCAR3-phosphopeptide + pIRS2-phosphopeptide)
3 · Its place in the literature

Who cites it

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

  1. Pooled it
  2. Trial
  3. Review
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  9. Immunoproteomics: The Evolution from Classical Methods to Emerging Techniques.Methods in molecular biology (Clifton, N.J.) · 2026
    Review
  10. Article
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  18. Article
  19. Review
  20. Tumor Antigens beyond the Human Exome.International journal of molecular sciences · 2024
    Review
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

21 authors at 3 institutions in 2 countries.

Victor H Engelhard *Beirne Carter Center for Immunology Research and Department of Microbiology, Immunology, and Cancer Biology, University of Virginia School of Medicine, Charlottesville, Virginia, USA vhe@virginia.edu.ORCID 0000-0002-1741-0925
Rebecca C Obeng *Beirne Carter Center for Immunology Research and Department of Microbiology, Immunology, and Cancer Biology, University of Virginia School of Medicine, Charlottesville, Virginia, USA.ORCID 0000-0001-8624-7108
Kara L Cummings *Beirne Carter Center for Immunology Research and Department of Microbiology, Immunology, and Cancer Biology, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Gina R Petroni *Department of Public Health Sciences, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Angela L Ambakhutwala *Beirne Carter Center for Immunology Research and Department of Microbiology, Immunology, and Cancer Biology, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Kimberly A Chianese-Bullock *Department of Surgery/Division of Surgical Oncology, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Kelly T SmithDepartment of Surgery/Division of Surgical Oncology, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Amanda LuluBeirne Carter Center for Immunology Research and Department of Microbiology, Immunology, and Cancer Biology, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Nikole VarhegyiDepartment of Public Health Sciences, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Mark E SmolkinDepartment of Public Health Sciences, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Paisley MyersDepartment of Chemistry, University of Virginia, Charlottesville, Virginia, USA.
Keira E MahoneyDepartment of Chemistry, University of Virginia, Charlottesville, Virginia, USA.
Jeffrey ShabanowitzDepartment of Chemistry, University of Virginia, Charlottesville, Virginia, USA.
Nico Buettner7Medical Research Council Centre for Immune Regulation and Clinical Immunology Service, University of Birmingham College of Medical and Dental Sciences, Birmingham, UK.
Emily H HallOffice of Clinical Research, University Virginia Cancer Center, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Kathleen HadenDepartment of Surgery/Division of Surgical Oncology, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Mark Cobbold7Medical Research Council Centre for Immune Regulation and Clinical Immunology Service, University of Birmingham College of Medical and Dental Sciences, Birmingham, UK.
Donald F HuntDepartment of Chemistry, University of Virginia, Charlottesville, Virginia, USA.
Geoffrey WeissMedicine/Division of Hematology-Oncology, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Elizabeth GaughanMedicine/Division of Hematology-Oncology, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Craig L SlingluffDepartment of Surgery/Division of Surgical Oncology, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
University of Virginia · USCarter Center · USImmune Regulation (United Kingdom) · GB

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Thomas P. Loughran · 1987 to 2026
$72.1M
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
PROCESSED ANTIGEN CHARACTERIZATION BY MASS SPECTROMETRYR01AI033993 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI HUNT, DONALD F · 1994 to 2017
$4.9M
Antigenic Determinants on HLA-B7 and -A2R01CA134060 · NCI · UNIVERSITY OF VIRGINIA · PI ENGELHARD, VICTOR H · 2008 to 2012
$2.4M
ANTIGENIC DETERMINANTS ON HLA-B7 AND -A2R01AI020963 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ENGELHARD, VICTOR H · 1985 to 2006
$1.8M
Immunity to MHC-restricted phosphopeptides in healthy donors and cancer patientsR01CA190665 · NCI · UNIVERSITY OF VIRGINIA · PI ENGELHARD, VICTOR H · 2014 to 2018
$1.8M
MINORITY PREDOCTORAL FELLOWSHIP PROGRAMF31CA119954 · NCI · UNIVERSITY OF VIRGINIA · PI OBENG, REBECCA CYNTHIA · 2006 to 2010
$154k
NCI NIH HHS F31 CA119954NCI NIH HHS P30 CA044579NCI NIH HHS R01 CA134060NCI NIH HHS R01 CA190665NCI NIH HHS T32 CA009109NIAID NIH HHS R01 AI020963NIAID NIH HHS R01 AI033993
6 · The paper itself

Abstract

backgroundPhosphorylated peptides presented by MHC molecules represent a new class of neoantigens expressed on cancer cells and recognized by CD8 T-cells. These peptides are promising targets for cancer immunotherapy. Previous work identified an HLA-A*0201-restricted phosphopeptide from insulin receptor substrate 2 (pIRS2) as one such target. The purpose of this study was to characterize a second phosphopeptide, from breast cancer antiestrogen resistance 3 (BCAR3), and to evaluate safety and immunogenicity of a novel immunotherapic vaccine comprising either or both of these phosphorylated peptides.

methodsPhosphorylated BCAR3 protein was evaluated in melanoma and breast cancer cell lines by Western blot, and recognition by T-cells specific for HLA-A*0201-restricted phosphorylated BCAR3 peptide (pBCAR3

resultspBCAR3 peptides were immunogenic in vivo in mice, and in vitro in normal human donors, and T-cells specific for pBCAR3

conclusionThis study supports the safety and immunogenicity of vaccines containing the cancer-associated phosphopeptides pBCAR3 TRIAL REGISTRATION NUMBER: NCT01846143.

Indexed as

Adaptor Proteins, Signal TransducingAdultAgedAged, 80 and overAnimalsAntigens, NeoplasmCancer VaccinesCD8-Positive T-LymphocytesCell Line, TumorFemaleGuanine Nucleotide Exchange FactorsHLA-A2 AntigenHumansImmunogenicity, VaccineImmunotherapyInsulin Receptor Substrate ProteinsAdaptor Proteins, Signal TransducingAntigens, NeoplasmBCAR3 protein, humanCancer VaccinesGuanine Nucleotide Exchange FactorsHLA-A*02:01 antigenHLA-A2 AntigenInsulin Receptor Substrate ProteinsIRS2 protein, humanPhosphopeptidesVaccines, Subunitantigensimmunogenicityimmunotherapymelanomaneoplasmvaccinationvaccine

Identifiers

PMID32385144
PMCPMC7228659
OpenAlexW3022287679

What OpenQuestion holds

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LicenceCC BY-NC
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.