Evidence map›Paper›PMID 31655796›Full record

ArticleAging2019

Immature dendritic cells derived exosomes promotes immune tolerance by regulating T cell differentiation in renal transplantation.

Xin-Lu Pang, Zhi-Gang Wang, Lei Liu, Yong-Hua Feng, Jun-Xiang Wang, Hong-Chang Xie, Xian-Lei Yang, Jin-Feng Li, Gui-Wen Feng

Open access · greenAbstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

46 citing papers in PubMed, 77 citations in OpenAlex.

  1. Review
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  3. Pathogens (Basel, Switzerland) · 2026
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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

9 authors at 1 institution in 1 country.

Xin-Lu PangDepartment of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Zhi-Gang WangDepartment of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Lei LiuDepartment of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Yong-Hua FengDepartment of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Jun-Xiang WangDepartment of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Hong-Chang XieDepartment of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Xian-Lei YangDepartment of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Jin-Feng LiDepartment of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Gui-Wen FengDepartment of Kidney Transplantation, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
First Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the mechanism of immature dendritic cells-derived exosomes (imDECs) in the regulation of T cell differentiation and immune tolerance in renal allograft model mice.

resultsimDECs significantly improved the percent of survival, relieved inflammatory response, and reduced CD4+T cell infiltration. In addition, imDECs reduced the rejection associated cytokines in allograft mice, and increased the percentage of Foxp3+CD4+T cells in spleen and kidney tissues. imDECs suppressed the IL17+CD4+T cells and promoted the Foxp3+CD4+T cells under Th17 polarization condition. Moreover, miR-682 was found to be highly expressed in imDECs which suppressed the IL17+CD4+T cells and promoted the Foxp3+CD4+T cells. Luciferase reporter assay showed ROCK2 was a target of miR-682, and ROCK mRNA level was negative correlated with miR-682 mRNA level.

conclusionmiR-682 was highly expressed in imDECs, and imDECs-secreted miR-682 promoted Treg cell differentiation by negatively regulating ROCK2 to promote immune tolerance in renal allograft model mice.

methodsRenal allograft model mice were established, and imDECs or mature dendritic cells-derived exosomes (mDECs) were injected into model mice. Rejection associated cytokines IFN-γ, IL-2, IL-17 levels in plasma were detected by ELISA. IL-17A, Foxp3, miR-682, ROCK2, p-STAT3, p-STAT5 expressions were measured by qRT-PCR or western blot.

Indexed as

Kidney TransplantationAnimalsCD4-Positive T-LymphocytesCell DifferentiationCytokinesDendritic CellsExosomesFemaleGene Expression RegulationGraft RejectionLymphocyte ActivationMaleMiceMice, Inbred BALB CMice, Inbred C57BLMicroRNAsCytokinesMicroRNAsexosomeimmature dendritic cellsmiR-682ROCK2T cell differentiation

Identifiers

PMID31655796
PMCPMC6834404
OpenAlexW2981955556

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.