Evidence map›Paper›PMID 23587571›Full record

ArticleImmunobiology2013

Intravenous transfer of apoptotic cell-treated dendritic cells leads to immune tolerance by blocking Th17 cell activity.

Fang Zhou, Elisabetta Lauretti, Antonio di Meco, Bogoljub Ciric, Patricia Gonnella, Guang-Xian Zhang, Abdolmohamad Rostami

Open access · greenAbstract read
In one paragraph

Article in Immunobiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
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  8. Selective depletion of CD11cEuropean journal of immunology · 2016
    Article
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  10. Review
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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

7 authors at 1 institution in 1 country.

Fang ZhouDepartment of Neurology, Thomas Jefferson University, 900 Walnut Street, Philadelphia, PA 19107, USA. fang.zhou@uqconnect.edu.au
Elisabetta Lauretti
Antonio di Meco
Bogoljub Ciric
Patricia Gonnella
Guang-Xian Zhang
Abdolmohamad Rostami
Thomas Jefferson University · US

Funding

The Role of Dendritic Cells in Intravenous ToleranceR01NS048435 · NINDS · THOMAS JEFFERSON UNIVERSITY · PI ROSTAMI, A.M. · 2004 to 2013
$2.9M
The Role of the TH17 cells in the pathogenesis of EAER01NS046782 · NINDS · THOMAS JEFFERSON UNIVERSITY · PI ROSTAMI, A.M. · 2003 to 2013
$2.7M
NINDS NIH HHS R01 NS046782NINDS NIH HHS R01 NS048435
6 · The paper itself

Abstract

Apoptotic cell-induced tolerogenic dendritic cells (DCs) play an important role in induction of peripheral tolerance in vivo; however, the mechanisms of immune tolerance induced by these DCs are poorly understood. Here we show that treatment of apoptotic cells modulates expression of inflammation- and tolerance-associated molecules including Gr-1, B220, CD205 and galectin-1 on bone marrow-derived DCs. In addition, apoptotic cell-treated DCs suppress secretion of cytokines produced by Th17 cells. Our data also demonstrate that i.v. transfer of apoptotic cell-treated DCs blocks EAE development and down-regulates production of inflammatory cytokines such as IL-17A and IL-17F in CD4+ T cells. These results suggest that apoptotic cell-treated DCs may inhibit activity of Th17 cells via down-regulation of inflammatory cytokine production, thereby affecting EAE development in vivo. Our results reveal a potential mechanism of immune tolerance mediated by apoptotic cell-treated DCs and the possible use of apoptotic cell-treated DCs to treat autoimmune diseases such as MS/EAE.

Indexed as

AnimalsAntigens, CDApoptosisBone Marrow CellsCell DifferentiationCells, CulturedCytokinesDendritic CellsEncephalomyelitis, Autoimmune, ExperimentalFemaleGalectin 1Immune ToleranceImmunotherapyLectins, C-TypeLeukocyte Common AntigensMiceAntigens, CDCytokinesDEC-205 receptorGalectin 1Gr-1 protein, mouseLectins, C-TypeLeukocyte Common AntigensMinor Histocompatibility AntigensMyelin-Oligodendrocyte Glycoproteinmyelin oligodendrocyte glycoprotein (35-55)Peptide FragmentsReceptors, Cell SurfaceReceptors, Chemokine

Identifiers

PMID23587571
PMCPMC3715992
OpenAlexW1996573718

What OpenQuestion holds

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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.