Evidence map›Paper›PMID 31488076›Full record

ArticleBMC nephrology2019

Vasoactive intestinal peptide ameliorates renal injury in a pristane-induced lupus mouse model by modulating Th17/Treg balance.

Dongdong Fu, Soulixay Senouthai, Junjie Wang, Yanwu You

Open access · goldAbstract read
In one paragraph

Article in BMC nephrology, 2019. 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
2.2field-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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Lactobacillus plantarum CQPC02 intervenes in mouse lupus nephritis by regulating the NF-κB signaling pathway.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Effects ofDrug design, development and therapy · 2022
    Article
  9. Article
  10. 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

4 authors at 1 institution in 1 country.

Dongdong FuDepartment of Nephrology, Affiliated Hospital of Youjiang Medical University for Nationalities, No. 18 Zhongshan Road II, Baise, 533000, Guangxi Zhuang Autonomous Region, China.
Soulixay SenouthaiDepartment of Nephrology, Affiliated Hospital of Youjiang Medical University for Nationalities, No. 18 Zhongshan Road II, Baise, 533000, Guangxi Zhuang Autonomous Region, China.
Junjie WangDepartment of Nephrology, Affiliated Hospital of Youjiang Medical University for Nationalities, No. 18 Zhongshan Road II, Baise, 533000, Guangxi Zhuang Autonomous Region, China.
Yanwu YouDepartment of Nephrology, Affiliated Hospital of Youjiang Medical University for Nationalities, No. 18 Zhongshan Road II, Baise, 533000, Guangxi Zhuang Autonomous Region, China. youyanwu@163.com.ORCID 0000-0002-2612-5317
Affiliated Hospital of Youjiang Medical University for Nationalities · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLupus nephritis (LN) is an inflammation of the kidneys and is a major cause of mortality in systemic lupus erythaematosus (SLE) patients. In addition, Th17/Treg balance is one of the most important factors that can promote the development of LN. It has been reported that vasoactive intestinal peptide (VIP) is associated with the downregulation of both inflammatory and autoimmune diseases through regulating T lymphocyte balance. Therefore, the aim of this study was to determine the role of VIP in modulating Th17/Treg balance in LN.

methodsLN was induced in BALB/c female mice by injection pristane. After 3 months, mice were randomly divided into four groups: control, VIP + control, LN and VIP + LN. Autoantibody levels were tested by ELISA. The distribution of Th17/Treg cells in vivo and in vitro was detected by FC. Renal tissues were examined by PASM and DIF for pathology and Foxp3

resultsVIP can improve renal injury by regulating Th17/Treg imbalance in LN mice. Proteinuria, renal function defects and autoantibodies were significantly decreased, and Th17/Treg cell balance was restored in VIP compared with LN mice. In addition, VIP improved renal lesions by promoting the expression of Foxp3

conclusionsVIP reduced LN proteinuria and renal function defects and restored the Th17/Treg cell balance. Furthermore, VIP also downregulated autoantibody and inflammatory cytokine expression and upregulated Foxp3 and IL-10 expression.

Indexed as

AnimalsDisease Models, AnimalFemaleLupus NephritisMiceMice, Inbred BALB CTerpenesTh17 CellsT-Lymphocytes, RegulatoryVasoactive Intestinal PeptidepristaneTerpenesVasoactive Intestinal PeptideLupus nephritisTh17/Treg balanceVasoactive intestinal peptide

Identifiers

PMID31488076
PMCPMC6728947
OpenAlexW2972042927

What OpenQuestion holds

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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.