Evidence map›Paper›PMID 26834749›Full record

ArticleFrontiers in immunology2016

Tolerogenic IDO(+) Dendritic Cells Are Induced by PD-1-Expressing Mast Cells.

Cecilia Pessoa Rodrigues, Ana Carolina Franco Ferreira, Mariana Pereira Pinho, Cristiano Jacob de Moraes, Patrícia Cruz Bergami-Santos, José Alexandre Marzagão Barbuto

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Tumor-infiltrating mast cells stimulate ICOSJournal of advanced research · 2024
    Article
  7. Article
  8. PD-1Cancer immunology, immunotherapy : CII · 2023
    Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Targeting the IDO1 pathway in cancer: from bench to bedside.Journal of hematology & oncology · 2018
    Review
  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

6 authors at 1 institution in 1 country.

Cecilia Pessoa RodriguesLaboratory of Tumor Immunology, Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo , São Paulo , Brazil.
Ana Carolina Franco FerreiraLaboratory of Tumor Immunology, Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo , São Paulo , Brazil.
Mariana Pereira PinhoLaboratory of Tumor Immunology, Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo , São Paulo , Brazil.
Cristiano Jacob de MoraesLaboratory of Tumor Immunology, Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo , São Paulo , Brazil.
Patrícia Cruz Bergami-SantosLaboratory of Tumor Immunology, Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo , São Paulo , Brazil.
José Alexandre Marzagão BarbutoLaboratory of Tumor Immunology, Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo, São Paulo, Brazil; Center for Cellular and Molecular Studies and Therapy (NETCEM), University of Sao Paulo, São Paulo, Brazil.
Universidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mast cells (MCs) are tissue resident cells, rich in inflammatory mediators, involved in allergic reactions, and with an increasingly recognized role in immunomodulation. Dendritic cells (DCs), on the other hand, are central to the determination of immune response patterns, being highly efficient antigen-presenting cells that respond promptly to changes in their microenvironment. Here, we show that direct cell contact between immature monocyte-derived DCs (iDCs) and MC bends DCs toward tolerance induction. DCs that had direct contact with MC (MC-iDC) decreased HLA-DR but increased PD-L1 expression and stimulated regulatory T lymphocytes, which expresses FoxP3(+), secrete TGF-β and IL-10, and suppress the proliferation of mitogen-stimulated naïve T lymphocytes. Furthermore, MC-iDC expressed higher levels of indoleamine-2,3-deoxigenase (IDO), a phenomenon that was blocked by treatment of MC with anti-PD-1 or by the treatment of DCs with anti-PD-L1 or anti-PD-L2, but not by blocking of H1 and H2 histamine receptors on DCs. Contact with MC also increased phosphorylated STAT-3 levels in iDCs. When a STAT-3 inhibitor, JSI-124, was added to the DCs before contact with MC, the MC-iDC recovered their ability to induce allogeneic T cell proliferation and did not increase their IDO expression.

Indexed as

IDOmast cellsSTAT-3tolerogenic DCsTregs

Identifiers

PMID26834749
PMCPMC4724729
OpenAlexW2259545109

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.