Evidence map›Paper›PMID 26539197›Full record

ReviewFrontiers in immunology2015

Role of Dendritic Cells in the Induction of Lymphocyte Tolerance.

Fabiola Osorio, Camila Fuentes, Mercedes N López, Flavio Salazar-Onfray, Fermín E González

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Medical Gas Plasma Jet Technology Targets Murine Melanoma in an Immunogenic Fashion.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    Article
  10. Targeting T cell activation in immuno-oncology.Current oncology (Toronto, Ont.) · 2020
    Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Influence of ovarian cancer type I and type II microenvironment on the phenotype and function of monocyte-derived dendritic cells.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2017
    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

5 authors.

Fabiola OsorioMillennium Institute on Immunology and Immunotherapy, Faculty of Medicine, University of Chile , Santiago , Chile ; Disciplinary Program of Immunology, Institute of Biomedical Sciences, Faculty of Medicine, University of Chile , Santiago , Chile.
Camila FuentesMillennium Institute on Immunology and Immunotherapy, Faculty of Medicine, University of Chile , Santiago , Chile ; Disciplinary Program of Immunology, Institute of Biomedical Sciences, Faculty of Medicine, University of Chile , Santiago , Chile.
Mercedes N LópezMillennium Institute on Immunology and Immunotherapy, Faculty of Medicine, University of Chile , Santiago , Chile ; Disciplinary Program of Immunology, Institute of Biomedical Sciences, Faculty of Medicine, University of Chile , Santiago , Chile ; Cell Therapy Laboratory, Blood Bank Service, University of Chile Clinical Hospital , Santiago , Chile.
Flavio Salazar-OnfrayMillennium Institute on Immunology and Immunotherapy, Faculty of Medicine, University of Chile , Santiago , Chile ; Disciplinary Program of Immunology, Institute of Biomedical Sciences, Faculty of Medicine, University of Chile , Santiago , Chile.
Fermín E GonzálezMillennium Institute on Immunology and Immunotherapy, Faculty of Medicine, University of Chile , Santiago , Chile ; Laboratory of Experimental Immunology and Cancer, Faculty of Dentistry, University of Chile , Santiago , Chile.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability of dendritic cells (DCs) to trigger tolerance or immunity is dictated by the context in which an antigen is encountered. A large body of evidence indicates that antigen presentation by steady-state DCs induces peripheral tolerance through mechanisms such as the secretion of soluble factors, the clonal deletion of autoreactive T cells, and feedback control of regulatory T cells. Moreover, recent understandings on the function of DC lineages and the advent of murine models of DC depletion have highlighted the contribution of DCs to lymphocyte tolerance. Importantly, these findings are now being applied to human research in the contexts of autoimmune diseases, allergies, and transplant rejection. Indeed, DC-based immunotherapy research has made important progress in the area of human health, particularly in regards to cancer. A better understanding of several DC-related aspects including the features of DC lineages, milieu composition, specific expression of surface molecules, the control of signaling responses, and the identification of competent stimuli able to trigger and sustain a tolerogenic outcome will contribute to the success of DC-based immunotherapy in the area of lymphocyte tolerance. This review will discuss the latest advances in the biology of DC subtypes related to the induction of regulatory T cells, in addition to presenting current ex vivo protocols for tolerogenic DC production. Particular attention will be given to the molecules and signals relevant for achieving an adequate tolerogenic response for the treatment of human pathologies.

Indexed as

DC-based immunotherapydendritic cellsFoxp3regulatory T cellstolerance

Identifiers

PMID26539197
PMCPMC4611163

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.