Evidence map›Paper›PMID 30800002›Full record

ArticleMediators of inflammation2019

Interleukin 10 Gene-Modified Bone Marrow-Derived Dendritic Cells Attenuate Liver Fibrosis in Mice by Inducing Regulatory T Cells and Inhibiting the TGF-

Yejin Xu, Xinyue Tang, Min Yang, Shengguo Zhang, Shanshan Li, Yukai Chen, Minhui Liu, Yuxiang Guo, Mingqin Lu

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2019. 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
2.1field-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

22 citing papers in PubMed, 41 citations in OpenAlex.

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  15. Article
  16. Pathogenesis from Inflammation to Cancer in NASH-Derived HCC.Journal of hepatocellular carcinoma · 2022
    Review
  17. Indole-3-propionic Acid-aggravated CClJournal of clinical and translational hepatology · 2021
    Article
  18. Article
  19. Review
  20. 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 1 country.

Yejin XuDepartment of Infectious Diseases, Jinhua Municipal Central Hospital, Jinhua, Zhejiang, China.
Xinyue TangDepartment of Gastroenterology, the First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.
Min YangDepartment of Infectious Disease, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou Key Laboratory of Hepatology, Institute of Hepatology, Wenzhou Medical University, Wenzhou, 325000 Zhejiang, China.
Shengguo ZhangDepartment of Infectious Disease, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou Key Laboratory of Hepatology, Institute of Hepatology, Wenzhou Medical University, Wenzhou, 325000 Zhejiang, China.
Shanshan LiDepartment of Infectious Disease, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou Key Laboratory of Hepatology, Institute of Hepatology, Wenzhou Medical University, Wenzhou, 325000 Zhejiang, China.
Yukai ChenDepartment of Infectious Disease, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou Key Laboratory of Hepatology, Institute of Hepatology, Wenzhou Medical University, Wenzhou, 325000 Zhejiang, China.
Minhui LiuDepartment of Infectious Diseases, Jinhua Municipal Central Hospital, Jinhua, Zhejiang, China.
Yuxiang GuoDepartment of Infectious Diseases, Jinhua Municipal Central Hospital, Jinhua, Zhejiang, China.
Mingqin LuDepartment of Infectious Disease, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou Key Laboratory of Hepatology, Institute of Hepatology, Wenzhou Medical University, Wenzhou, 325000 Zhejiang, China.ORCID 0000-0002-8331-5862
Wenzhou Medical University · CNJinhua Central Hospital · CNFirst Affiliated Hospital of Gannan Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo explore the therapeutic effects and mechanisms of interleukin 10 gene-modified bone marrow-derived dendritic cells (DC-IL10) on liver fibrosis.

methodsIn vitro, BMDCs were transfected with lentiviral-interleukin 10-GFP (LV-IL10-GFP) at the MOI of 1 : 40. Then, the phenotype (MHCII, CD80, and CD86) and allo-stimulatory ability of DC-IL10 were identified by flow cytometry, and the levels of IL-10 and IL-12 (p70) secreted into the culture supernatants were quantified by ELISA. In vivo, DC-IL10 was injected into mice with CCl4-induced liver fibrosis through the tail vein. Lymphocytes were isolated to investigate the differentiation of T cells, and serum and liver tissue were collected for biochemical, cytokine, histopathologic, immune-histochemical, and Western blot analyzes.

resultsIn vitro, the expressions of MHCII, CD80, and CD86 in DC-IL10 were significantly suppressed, allogeneic CD4

conclusionIL-10 genetic modification of BMDCs may maintain DC in the state of tolerance and allow DC to induce T cell hyporesponsiveness or tolerance. DC-IL10 suppressed liver fibrosis by inducing Treg production and inhibiting the TGF-

Indexed as

AnimalsBone Marrow CellsCell DifferentiationDendritic CellsInterleukin-10Liver CirrhosisMaleMiceMice, Inbred BALB CMice, Inbred C57BLSmad ProteinsT-Lymphocytes, RegulatoryTransforming Growth Factor betaInterleukin-10Smad ProteinsTransforming Growth Factor beta

Identifiers

PMID30800002
PMCPMC6360045
OpenAlexW2910070149

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.