Evidence map›Paper›PMID 26341385›Full record

ArticleJournal of autoimmunity2016

pDC therapy induces recovery from EAE by recruiting endogenous pDC to sites of CNS inflammation.

Fernanda V Duraes, Carla Lippens, Karin Steinbach, Juan Dubrot, Dale Brighouse, Nathalie Bendriss-Vermare, Shohreh Issazadeh-Navikas, Doron Merkler, Stephanie Hugues

Open access · hybridAbstract read
In one paragraph

Article in Journal of autoimmunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

22 citing papers in PubMed, 39 citations in OpenAlex.

  1. Paradoxical Expression of Ionotropic Glutamate Receptors in Leucocytes.Clinical reviews in allergy & immunology · 2026
    Article
  2. Frontiers in cellular neuroscience · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Inhibition of the BMP Signaling Pathway Ameliorated Established Clinical Symptoms of Experimental Autoimmune Encephalomyelitis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2020
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. SLAMF9 regulates pDC homeostasis and function in health and disease.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  17. Article
  18. Autoimmunity in 2016.Clinical reviews in allergy & immunology · 2017
    Review
  19. Review
  20. Dendritic cell migration in health and disease.Nature reviews. Immunology · 2017
    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

9 authors at 3 institutions in 3 countries.

Fernanda V DuraesDepartment of Pathology and Immunology, University of Geneva, 1211 Geneva 4, Switzerland.
Carla LippensDepartment of Pathology and Immunology, University of Geneva, 1211 Geneva 4, Switzerland.
Karin SteinbachDepartment of Pathology and Immunology, University of Geneva, 1211 Geneva 4, Switzerland.
Juan DubrotDepartment of Pathology and Immunology, University of Geneva, 1211 Geneva 4, Switzerland.
Dale BrighouseDepartment of Pathology and Immunology, University of Geneva, 1211 Geneva 4, Switzerland.
Nathalie Bendriss-VermareUniversité Lyon 1, INSERM U1052, CNRS, UMR5286, Centre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, LabEx DEVweCAN, Lyon, France.
Shohreh Issazadeh-NavikasBiotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark.
Doron MerklerDepartment of Pathology and Immunology, University of Geneva, 1211 Geneva 4, Switzerland; Department of Pathology and Immunology, Division of Clinical Pathology, University & University Hospital of Geneva, Switzerland.
Stephanie HuguesDepartment of Pathology and Immunology, University of Geneva, 1211 Geneva 4, Switzerland. Electronic address: Stephanie.hugues@unige.ch.
University of Geneva · CHCentre National de la Recherche Scientifique · FRUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasmacytoid dendritic cells (pDCs) exhibit both innate and adaptive functions. In particular they are the main source of type I IFNs and directly impact T cell responses through antigen presentation. We have previously demonstrated that during experimental autoimmune encephalomyelitis (EAE) initiation, myelin-antigen presentation by pDCs is associated with suppressive Treg development and results in attenuated EAE. Here, we show that pDCs transferred during acute disease phase confer recovery from EAE. Clinical improvement is associated with migration of injected pDCs into inflamed CNS and is dependent on the subsequent and selective chemerin-mediated recruitment of endogenous pDCs to the CNS. The protective effect requires pDC pre-loading with myelin antigen, and is associated with the modulation of CNS-infiltrating pDC phenotype and inhibition of CNS encephalitogenic T cells. This study may pave the way for novel pDC-based cell therapies in autoimmune diseases, aiming at specifically modulating pathogenic cells that induce and sustain autoimmune inflammation.

Indexed as

Adoptive TransferAnimalsAutoantigensCell- and Tissue-Based TherapyChemokinesChemotaxisDendritic CellsDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalIntercellular Signaling Peptides and ProteinsMiceMice, KnockoutMyelin SheathReceptors, ChemokineReceptors, G-Protein-CoupledSpinal CordAutoantigenschemerin protein, mouseChemokinesCMKLR1 protein, mouseIntercellular Signaling Peptides and ProteinsReceptors, ChemokineReceptors, G-Protein-CoupledCell therapyCentral nervous systemExperimental autoimmune encephalomyelitisPlasmacytoid dendritic cells

Identifiers

PMID26341385
PMCPMC4758828
OpenAlexW1519413674

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.