Evidence map›Paper›PMID 33206750›Full record

ArticleClinics (Sao Paulo, Brazil)2020

Inhibition of lipopolysaccharide-induced inflammation via the protective role of T regulatory cells in the fetal liver in a late-pregnancy preterm mouse model.

Muhammad Siddiq, Fan Wang, Mi Xiao, Xiao Jie Lin, Nazira Fatima, Sara Iqbal, Umar Iqbal, Xian-Hua Piao, Li Liu

Open access · goldAbstract read
In one paragraph

Article in Clinics (Sao Paulo, Brazil), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 82% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. 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 4 institutions in 3 countries.

Muhammad SiddiqDepartment of Neonatology, The First Affiliated Hospital of Xi'an Jiaotong University College of Medicine, Xi'an, Shaanxi, China.ORCID 0000-0002-9891-9837
Fan WangDepartment of Neonatology, The First Affiliated Hospital of Xi'an Jiaotong University College of Medicine, Xi'an, Shaanxi, China.ORCID 0000-0001-7374-3567
Mi XiaoDepartment of Neonatology, The First Affiliated Hospital of Xi'an Jiaotong University College of Medicine, Xi'an, Shaanxi, China.ORCID 0000-0001-6474-2458
Xiao Jie LinDepartment of Neonatology, The First Affiliated Hospital of Xi'an Jiaotong University College of Medicine, Xi'an, Shaanxi, China.ORCID 0000-0001-6730-9342
Nazira FatimaDepartment of Biotechnology, Mirpur University of Science & Technology Pakistan, Pakistan and Laboratory Animal Center Xian Jiaotong University Health Science Centre, Xian Shaanxi, China.ORCID 0000-0002-7571-0440
Sara IqbalAkhtar Saeed Medical & Dental College, Akhtar Saeed Trust Hospital & Farooq Hospital Lahore, Akhtar Saeed Medical & Dental CollegeAkhtar Saeed Trust Hospital & Farooq Hospital LahorePakistanPakistan.ORCID 0000-0003-4027-1190
Umar IqbalAkhtar Saeed Medical & Dental College, Akhtar Saeed Trust Hospital & Farooq Hospital Lahore, Akhtar Saeed Medical & Dental CollegeAkhtar Saeed Trust Hospital & Farooq Hospital LahorePakistanPakistan.ORCID 0000-0003-2802-9238
Xian-Hua PiaoThe Division of Newborn Medicine, Boston Children's Hospital of Harvard Medical School, Boston, Massachusetts, U.S.A.ORCID 0000-0003-0412-517X
Li LiuDepartment of Neonatology, The First Affiliated Hospital of Xi'an Jiaotong University College of Medicine, Xi'an, Shaanxi, China.ORCID 0000-0003-1200-3068
First Affiliated Hospital of Xi'an Jiaotong University · CNFarooq Hospital · PKBoston Children's Hospital · USMirpur University of Science and Technology · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis study intended to explore the effect of T regulatory cells (Tregs) in the perinatal liver against LPS-induced inflammation in a preterm birth mouse model. Moreover, the role of adoptive Tregs on the inflammatory response induced by LPS was also studied.

methodsFemale BALB/C mice were injected intraperitoneally (IP) with LPS dissolved in normal saline solution at a dose of 50 µg/kg. Spleens from pregnant mice were used to obtain Tregs. The expression of Forkhead family transcription factor-3 (Foxp3), Interleukin-6 (IL-6), Toll-like receptor-4 (TLR-4), and Heme oxygenase-1 (HO-1) were assessed from fetal liver tissues by polymerase chain reaction and western blotting.

resultsLPS administered to mice induced an inflammatory response in the perinatal liver, and this inflammatory response was negatively regulated by Tregs in the experimental group. Maternal-fetal tolerance was maintained by Tregs. Transmission of Tregs was estimated in different experimental groups based on the mRNA expression of TLR-4, IL-6, HO-1, and Foxp3.

conclusionsAfter analysis of the experimental data, it was determined that Tregs exhibited regulatory potential against LPS-induced inflammatory response. Further, it was concluded that the transmission of Tregs improved the mother's immune tolerance against LPS-induced inflammation in the fetal liver.

Indexed as

LipopolysaccharidesPremature BirthAnimalsFemaleForkhead Transcription FactorsInflammationLiverMiceMice, Inbred BALB CPregnancyT-Lymphocytes, RegulatoryForkhead Transcription FactorsLipopolysaccharides

Identifiers

PMID33206750
PMCPMC7603294
OpenAlexW3103330800

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.