Evidence map›Paper›PMID 27558022›Full record

ArticleStem cell research & therapy2016

Establishing a tree shrew model of systemic lupus erythematosus and cell transplantation treatment.

Guang-Ping Ruan, Xiang Yao, Ju-Fen Liu, Jie He, Zi-An Li, Jian-Yong Yang, Rong-Qing Pang, Xing-Hua Pan

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Cross-sectional atlas of the tree shrew (Frontiers in veterinary science · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Tree shrew (Zoological research · 2017
    Review
  10. Article
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

8 authors at 1 institution in 1 country.

Guang-Ping RuanThe Cell Biological Therapy Center, Kunming General Hospital of Chengdu Military Command, Kunming, 650032, People's Republic of China. ruangp@126.com.
Xiang YaoThe Cell Biological Therapy Center, Kunming General Hospital of Chengdu Military Command, Kunming, 650032, People's Republic of China.
Ju-Fen LiuThe Cell Biological Therapy Center, Kunming General Hospital of Chengdu Military Command, Kunming, 650032, People's Republic of China.
Jie HeThe Cell Biological Therapy Center, Kunming General Hospital of Chengdu Military Command, Kunming, 650032, People's Republic of China.
Zi-An LiThe Cell Biological Therapy Center, Kunming General Hospital of Chengdu Military Command, Kunming, 650032, People's Republic of China.
Jian-Yong YangThe Cell Biological Therapy Center, Kunming General Hospital of Chengdu Military Command, Kunming, 650032, People's Republic of China.
Rong-Qing PangThe Cell Biological Therapy Center, Kunming General Hospital of Chengdu Military Command, Kunming, 650032, People's Republic of China.
Xing-Hua PanThe Cell Biological Therapy Center, Kunming General Hospital of Chengdu Military Command, Kunming, 650032, People's Republic of China. ynkmry@163.com.
Kunming General Hospital of Chengdu Military Command · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe establishment of a tree shrew model for systemic lupus erythematosus (SLE) provides a new method to evaluate the pathogenesis of autoimmune diseases.

methodsEighty tree shrews were randomly divided into four groups receiving either an intraperitoneal injection of pristane, lipopolysaccharide (LPS), or pristane and LPS, or no injection. Three weeks after injection, the SLE model tree shrews were divided into the model group and the treatment group. Tree shrews in the treatment group and the normal control group were infused with umbilical cord mesenchymal stem cells (UC-MSCs). The cells were labeled with DiR. Two weeks after transplantation, three groups of tree shrews were analyzed for urine protein, serum antinuclear antibodies and antiphospholipid, and inflammatory cytokine antibody microarray detection. The heart, liver, spleen, lung, and kidney were collected from the three groups and subjected to hematoxylin and eosin (HE) staining and detection of renal immune complex deposition.

resultsHE staining indicated pathology in the model group. Red fluorescence revealed immune complex deposition in the kidneys from the model group.

conclusionsThe combined intraperitoneal injection of pristane and LPS is the best way to induce SLE pathological changes. The pathological changes improved after UC-MSC treatment.

Indexed as

AnimalsDisease Models, AnimalInflammationLipopolysaccharidesLupus Erythematosus, SystemicMesenchymal Stem CellsMesenchymal Stem Cell TransplantationTerpenesTupaiidaeUmbilical CordLipopolysaccharidespristaneTerpenesAnimal modelsSystemic lupus erythematosusTransplantationTree shrewsUmbilical cord mesenchymal stem cells

Identifiers

PMID27558022
PMCPMC4995612
OpenAlexW2510331026

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.