Evidence map›Paper›PMID 23298832›Full record

ArticleThe Journal of clinical investigation2013

Specialized role of migratory dendritic cells in peripheral tolerance induction.

Juliana Idoyaga, Christopher Fiorese, Lori Zbytnuik, Ashira Lubkin, Jennifer Miller, Bernard Malissen, Daniel Mucida, Miriam Merad, Ralph M Steinman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 185 papers.

0numbers the graph read from it
0cells of the map it votes in
185citing papers in PubMed
15.3field-weighted citation impact, top 1% 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

185 citing papers in PubMed, 300 citations in OpenAlex.

  1. Review
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  6. Review
  7. Multiple sclerosis: molecular pathogenesis and therapeutic intervention.Signal transduction and targeted therapy · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Monocytes give rise to Langerhans cells that preferentially migrate to lymph nodes at steady state.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  18. Dendritic cells in food allergy, treatment, and tolerance.The Journal of allergy and clinical immunology · 2024
    Review
  19. Aire in Autoimmunity.Annual review of immunology · 2024
    Review
  20. Article

125 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

Juliana IdoyagaLaboratory of Cellular Physiology and Immunology and Chris Browne Center for Immunology and Immune Diseases, The Rockefeller University, New York, New York, USA. ijuliana@rockefeller.edu.
Christopher Fiorese
Lori Zbytnuik
Ashira Lubkin
Jennifer Miller
Bernard Malissen
Daniel Mucida
Miriam Merad
Ralph M Steinman
Rockefeller University · USInserm · FR

Funding

Properties of Mouse of Dendritic Cells and MacrophagesR01AI013013 · NIAID · ROCKEFELLER UNIVERSITY · PI MOJSOV, SVETLANA · 1985 to 2015
$8.9M
Mechanisms used by skin dendritic cells to induce regulatory T cellsK99AR062595 · NIAMS · ROCKEFELLER UNIVERSITY · PI IDOYAGA, JULIANA · 2012 to 2013
$191k
PROPERTIES OF MOUSE DENDRITIC CELLS AND MACROPHAGESR37AI013013 · NIAID · ROCKEFELLER UNIVERSITY · PI STEINMAN, RALPH M. · 1986 to 1995
–
NIAID NIH HHS AI13013NIAID NIH HHS R01 AI013013NIAMS NIH HHS 1K99AR062595NIAMS NIH HHS K99 AR062595
6 · The paper itself

Abstract

Harnessing DCs for immunotherapies in vivo requires the elucidation of the physiological role of distinct DC populations. Migratory DCs traffic from peripheral tissues to draining lymph nodes charged with tissue self antigens. We hypothesized that these DC populations have a specialized role in the maintenance of peripheral tolerance, specifically, to generate suppressive Foxp3+ Tregs. To examine the differential capacity of migratory DCs versus blood-derived lymphoid-resident DCs for Treg generation in vivo, we targeted a self antigen, myelin oligodendrocyte glycoprotein, using antibodies against cell surface receptors differentially expressed in these DC populations. Using this approach together with mouse models that lack specific DC populations, we found that migratory DCs have a superior ability to generate Tregs in vivo, which in turn drastically improve the outcome of experimental autoimmune encephalomyelitis. These results provide a rationale for the development of novel therapies targeting migratory DCs for the treatment of autoimmune diseases.

Indexed as

AnimalsAntigens, CDAntigens, SurfaceAutoantigensCell MovementDendritic CellsEncephalomyelitis, Autoimmune, ExperimentalForkhead Transcription FactorsLangerhans CellsLectins, C-TypeMannose-Binding LectinsMiceMice, KnockoutMinor Histocompatibility AntigensMyelin-Oligodendrocyte GlycoproteinPeripheral ToleranceAntigens, CDAntigens, SurfaceAutoantigensCd207 protein, mouseDcir protein, mouseDEC-205 receptorForkhead Transcription FactorsFoxp3 protein, mouseLectins, C-TypeMannose-Binding LectinsMinor Histocompatibility AntigensMog protein, mouseMyelin-Oligodendrocyte GlycoproteinReceptors, Cell SurfaceReceptors, ImmunologicTreml4 protein, mouse

Identifiers

PMID23298832
PMCPMC3561796
OpenAlexW2029771914

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.