Evidence map›Paper›PMID 32231867›Full record

ArticleOncoimmunology2020

Tumor endothelial cell up-regulation of IDO1 is an immunosuppressive feed-back mechanism that reduces the response to CD40-stimulating immunotherapy.

Maria Georganaki, Mohanraj Ramachandran, Sander Tuit, Nicolás Gonzalo Núñez, Alexandros Karampatzakis, Grammatiki Fotaki, Luuk van Hooren, Hua Huang, Roberta Lugano, Thomas Ulas and 8 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

30 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Linking tumour angiogenesis and tumour immunity.Nature reviews. Immunology · 2026
    Review
  6. Article
  7. Article
  8. Targeting Cancer: Microenvironment and Immunotherapy Innovations.International journal of molecular sciences · 2024
    Review
  9. The crossroad between tumor and endothelial cells.Clinical and experimental medicine · 2024
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Barriers to immune cell infiltration in tumors.Journal for immunotherapy of cancer · 2023
    Review
  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

18 authors at 5 institutions in 4 countries.

Maria GeorganakiDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Mohanraj RamachandranDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Sander TuitGenomics & Immunoregulation, Life and Medical Science Institute, University of Bonn, Bonn, Germany.
Nicolás Gonzalo NúñezInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
Alexandros KarampatzakisDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Grammatiki FotakiDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Luuk van HoorenDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Hua HuangDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Roberta LuganoDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Thomas UlasGenomics & Immunoregulation, Life and Medical Science Institute, University of Bonn, Bonn, Germany.ORCID 0000-0002-9785-4197
Aura KaunistoAlligator Bioscience, Medicon Village, Lund, Sweden.
Eric C HollandDivision of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Peter EllmarkAlligator Bioscience, Medicon Village, Lund, Sweden.
Sara M MangsboDepartment of Pharmaceutical Biosciences, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Joachim SchultzeGenomics & Immunoregulation, Life and Medical Science Institute, University of Bonn, Bonn, Germany.
Magnus EssandDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Sonia TuguesInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
Anna DimbergDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, The Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.ORCID 0000-0003-4422-9125
Uppsala University · SEUniversity of Bonn · DEMedicon Village · SEUniversity of Zurich · CHFred Hutch Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD40-stimulating immunotherapy can elicit potent anti-tumor responses by activating dendritic cells and enhancing T-cell priming. Tumor vessels orchestrate T-cell recruitment during immune response, but the effect of CD40-stimulating immunotherapy on tumor endothelial cells has not been evaluated. Here, we have investigated how tumor endothelial cells transcriptionally respond to CD40-stimulating immunotherapy by isolating tumor endothelial cells from agonistic CD40 mAb- or isotype-treated mice bearing B16-F10 melanoma, and performing RNA-sequencing. Gene set enrichment analysis revealed that agonistic CD40 mAb therapy increased interferon (IFN)-related responses in tumor endothelial cells, including up-regulation of the immunosuppressive enzyme Indoleamine 2, 3-Dioxygenase 1 (IDO1). IDO1 was predominantly expressed in endothelial cells within the tumor microenvironment, and its expression in tumor endothelium was positively correlated to T-cell infiltration and to increased intratumoral expression of IFNγ.

Indexed as

Indoleamine-Pyrrole 2,3,-DioxygenaseMelanoma, ExperimentalAnimalsEndothelial CellsEndotheliumImmunotherapyMiceTumor MicroenvironmentUp-RegulationIndoleamine-Pyrrole 2,3,-DioxygenaseCD40IDO1immunotherapymelanomatumor endothelial cells

Identifiers

PMID32231867
PMCPMC7094447
OpenAlexW2791050763

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.