Evidence map›Paper›PMID 31221818›Full record

ArticleBioscience reports2019

Mechanism of gut microbiota and Axl/SOCS3 in experimental autoimmune encephalomyelitis.

Xiao-Ling Li, Bo Zhang, Meng-Jiao Sun, Cai-Cai Bao, Bo-Yao Yuan, Qin-Fang Xie, Li-Juan Wang, Man-Xia Wang

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Xiao-Ling LiDepartment of Neurology, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Bo ZhangDepartment of Cardiovascular Medicine, The First Hospital of Lanzhou University, Lanzhou 730000, China.
Meng-Jiao SunDepartment of Neurology, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Cai-Cai BaoDepartment of Neurology, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Bo-Yao YuanDepartment of Neurology, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Qin-Fang XieDepartment of Neurology, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Li-Juan WangDepartment of Neurology, The Second Hospital of Lanzhou University, Lanzhou 730030, China.
Man-Xia WangDepartment of Neurology, The Second Hospital of Lanzhou University, Lanzhou 730030, China wmx322_med@126.com.ORCID 0000-0002-3501-5427
Lanzhou University Second Hospital · CNFirst Hospital of Lanzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is an immune-mediated disease of the central nervous system (CNS). The present study explored the role of intestinal microbiota in the initiation and propagation of mice induced by experimental autoimmune encephalomyelitis (EAE), an animal model of multiple sclerosis. 48 C57BL/6 were randomly divided into control group and EAE group. The changes of body weight and the scores of neurological function were recorded. The mRNA expression of the receptor tyrosine kinase subfamily (AXL) was detected by real-time quantitative PCR. The levels of IL-17 and IFN-γ in blood samples were examined by ELISA. The intestinal microbial composition of mice at different time points during the EAE induction was analyzed by 16S rRNA gene-based sequencing. In EAE group, the body weight began to reduce at day 3 and neurological symptoms began to appear at day 7 after EAE induction. The levels of IL-17 and IFN-γ in EAE group reached the peak at day 21 and then decreased gradually. However, the expression of Axl and SOCS3 reached the lowest level at day 21 and then increased gradually. The microbiome analyses revealed that the abundances of

Indexed as

AnimalsAxl Receptor Tyrosine KinaseCentral Nervous SystemCytokinesDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalEnzyme-Linked Immunosorbent AssayGastrointestinal MicrobiomeHumansInterleukin-17IntestinesMiceMultiple SclerosisProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesRNA, Ribosomal, 16SAxl Receptor Tyrosine KinaseCytokinesInterleukin-17Proto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesRNA, Ribosomal, 16SSocs3 protein, mouseSuppressor of Cytokine Signaling 3 Proteinexperimental autoimmune encephalomyelitisGut microbiotaInflammatory inhibitorsReceptor tyrosine kinase subfamily

Identifiers

PMID31221818
PMCPMC6603274
OpenAlexW2951045519

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.