Evidence map›Paper›PMID 28356164›Full record

ArticleArthritis research & therapy2017

Excessive activation of the TLR9/TGF-β1/PDGF-B pathway in the peripheral blood of patients with systemic lupus erythematosus.

Yi Yuan, Mingyue Yang, Kuo Wang, Jing Sun, Lili Song, Xue Diao, Zhenyu Jiang, Genhong Cheng, Xiaosong Wang

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 11% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
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  5. Molecular and Cellular Mediators of Renal Fibrosis in Lupus Nephritis.International journal of molecular sciences · 2025
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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 3 institutions in 2 countries.

Yi YuanInstitute of Translational Medicine, the First Hospital, Jilin University, Changchun, 130061, China.
Mingyue YangInstitute of Translational Medicine, the First Hospital, Jilin University, Changchun, 130061, China.
Kuo WangInstitute of Translational Medicine, the First Hospital, Jilin University, Changchun, 130061, China.
Jing SunShanghai Wisdom Chemical Research Co. Ltd., Shanghai, 201203, China.
Lili SongInstitute of Translational Medicine, the First Hospital, Jilin University, Changchun, 130061, China.
Xue DiaoInstitute of Translational Medicine, the First Hospital, Jilin University, Changchun, 130061, China.
Zhenyu JiangDepartment of Rheumatology and Immunology, the First Hospital, Jilin University, Changchun, 130021, China. jlujzy@aliyun.com.
Genhong ChengInstitute of Translational Medicine, the First Hospital, Jilin University, Changchun, 130061, China. gcheng@mednet.ucla.edu.
Xiaosong WangInstitute of Translational Medicine, the First Hospital, Jilin University, Changchun, 130061, China. zhuanhuawang@163.com.
Jilin University · CNFirst Hospital of Jilin University · CNUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOur aim is to study the existence of the TLR9/TGF-β1/PDGF-B pathway in healthy humans and patients with systemic lupus erythematosus (SLE), and to explore its possible involvement in the pathogenesis of lupus nephritis (LN).

methodsProtein levels of the cytokines were detected by ELISA. mRNA levels of the cytokines were analyzed by real-time PCR. MTT assay was used to test the proliferation of mesangial cells under different treatments.

resultsCompared to healthy controls (N

conclusionsThe TLR9/TGF-β1/PDGF-B pathway exists in humans and can be excessively activated in SLE patients. High levels of PDGF-B may result in overproliferation of mesangial cells in the kidney that are involved in the development of glomerulonephritis and LN. Further studies are necessary to identify TLR9, TGF-β1, and PDGF-B as new therapeutic targets to prevent the development of glomerulonephritis and LN.

Indexed as

Enzyme-Linked Immunosorbent AssayFemaleFlow CytometryHumansLupus Erythematosus, SystemicLupus NephritisMaleMesangial CellsMiddle AgedProto-Oncogene Proteins c-sisReal-Time Polymerase Chain ReactionSignal TransductionToll-Like Receptor 9Transforming Growth Factor beta1Proto-Oncogene Proteins c-sisTLR9 protein, humanToll-Like Receptor 9Transforming Growth Factor beta1Lupus nephritisSystemic lupus erythematosusToll-like receptor 9

Identifiers

PMID28356164
PMCPMC5372299
OpenAlexW2599514030

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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.