Evidence map›Paper›PMID 19008459›Full record

Trial reportBlood2009

Protein disulfide isomerases are antibody targets during immune-mediated tumor destruction.

Catia Fonseca, Robert Soiffer, Vincent Ho, Matthew Vanneman, Masahisa Jinushi, Jerome Ritz, Donna Neuberg, Richard Stone, Dan DeAngelo, Glenn Dranoff

Open access · bronzeAbstract readClinical TrialClinical Trial, Phase I
In one paragraph

Trial report in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Angiogenic cytokines are antibody targets during graft-versus-leukemia reactions.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Discovery of an orally active small-molecule irreversible inhibitor of protein disulfide isomerase for ovarian cancer treatment.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  17. Article
  18. Article
  19. Article
  20. Article
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

10 authors at 4 institutions in 1 country.

Catia FonsecaDepartment of Medical Oncology and Cancer Vaccine Center, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Robert Soiffer
Vincent Ho
Matthew Vanneman
Masahisa Jinushi
Jerome Ritz
Donna Neuberg
Richard Stone
Dan DeAngelo
Glenn Dranoff
Dana-Farber Cancer Institute · USBrigham and Women's Hospital · USDana-Farber Brigham Cancer Center · USHarvard University · US

Funding

TYROSINE KINASE ONCOGENESIS IN MYELOID LEUKEMIAP01CA066996 · NCI · DANA-FARBER CANCER INSTITUTE · PI SCOTT A ARMSTRONG · 1996 to 2026
$52.5M
NCI NIH HHS P01 CA066996
6 · The paper itself

Abstract

The identification of cancer antigens that contribute to transformation and are linked with immune-mediated tumor destruction is an important goal for immunotherapy. Toward this end, we screened a murine renal cell carcinoma cDNA expression library with sera from mice vaccinated with irradiated tumor cells engineered to secrete granulocyte macrophage colony-stimulating factor (GM-CSF). Multiple nonmutated, overexpressed proteins that function in tumor cell migration, protein/nucleic acid homeostasis, metabolism, and stress responses were detected. Among these, the most frequently recognized clone was protein disulfide isomerase (PDI). High titer antibodies to human PDI were similarly induced in an acute myeloid leukemia patient who achieved a complete response after vaccination with irradiated, autologous GM-CSF-secreting tumor cells in the setting of nonmyeloablative allogeneic bone marrow transplantation. Moreover, ERp5, a closely related disulfide isomerase involved in major histocompatibility complex (MHC) class I chain-related protein A (MICA) shedding, also evoked potent humoral reactions in diverse solid and hematologic malignancy patients who responded to GM-CSF-secreting tumor cell vaccines or antibody blockade of cytotoxic T lymphocyte-associated antigen 4 (CTLA-4). Together, these findings reveal the unexpected immunogenicity of PDIs and raise the possibility that these gene products might serve as targets for therapeutic monoclonal antibodies.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CDAntigens, NeoplasmBone Marrow TransplantationCancer VaccinesCarcinoma, Renal CellCell Line, TumorCTLA-4 AntigenFemaleGene LibraryGranulocyte-Macrophage Colony-Stimulating FactorHistocompatibility Antigens Class IHumansKidney NeoplasmsLeukemia, MyeloidAntibodies, MonoclonalAntigens, CDAntigens, NeoplasmCancer VaccinesCTLA-4 AntigenCTLA4 protein, humanCtla4 protein, mouseGranulocyte-Macrophage Colony-Stimulating FactorHistocompatibility Antigens Class IPDIA6 protein, humanProtein Disulfide-Isomerases

Identifiers

PMID19008459
PMCPMC2647666
OpenAlexW2064826198

What OpenQuestion holds

Textmetadata
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.