Evidence map›Paper›PMID 31730485›Full record

ArticleStem cell research & therapy2019

Treatment of the bone marrow stromal stem cell supernatant by nasal administration-a new approach to EAE therapy.

Xi Wang, Wantong Zhai, Jiahui Zhu, Wei Zhao, Xiaoyi Zou, Siying Qu, Shenyue Wang, Zhongze He, Zhaoying Li, Lingyang Wang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Article
  5. Article
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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

12 authors at 2 institutions in 1 country.

Xi WangDepartment of Neurobiology, Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Wantong ZhaiDepartment of Neurobiology, Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Jiahui ZhuDepartment of Neurobiology, Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Wei ZhaoDepartment of Neurobiology, Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Xiaoyi ZouDepartment of Neurobiology, Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Siying QuDepartment of Neurobiology, Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Shenyue WangDepartment of Neurobiology, Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Zhongze HeDepartment of Neurobiology, Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Zhaoying LiThe Key Laboratory of Myocardial Ischemia, Harbin Medical University, Ministry of Education, Harbin, 150086, Heilongjiang, China.
Lingyang WangDepartment of Neurobiology, Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Bo SunDepartment of Neurobiology, Harbin Medical University, Harbin, 150086, Heilongjiang, China. sunbo@hrbmu.edu.cn.
Hulun LiDepartment of Neurobiology, Harbin Medical University, Harbin, 150086, Heilongjiang, China. lihl@hrbmu.edu.cn.
Harbin Medical University · CNSecond Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMultiple sclerosis (MS) is one of the most common autoimmune diseases of the central nervous system (CNS). CNS has its own unique structural and functional features, while the lack of precision regulatory element with high specificity as therapeutic targets makes the development of disease treatment in the bottleneck. Recently, the immunomodulation and neuroprotection capabilities of bone marrow stromal stem cells (BMSCs) were shown in experimental autoimmune encephalomyelitis (EAE). However, the administration route and the safety evaluation limit the application of BMSC. In this study, we investigated the therapeutic effect of BMSC supernatant by nasal administration.

methodsIn the basis of the establishment of the EAE model, the BMSC supernatant were treated by nasal administration. The clinical score and weight were used to determine the therapeutic effect. The demyelination of the spinal cord was detected by LFB staining. ELISA was used to detect the expression of inflammatory factors in serum of peripheral blood. Flow cytometry was performed to detect pro-inflammatory cells in the spleen and draining lymph nodes.

resultsBMSC supernatant by nasal administration can alleviate B cell-mediated clinical symptoms of EAE, decrease the degree of demyelination, and reduce the inflammatory cells infiltrated into the central nervous system; lessen the antibody titer in peripheral bloods; and significantly lower the expression of inflammatory factors. As a new, non-invasive treatment, there are no differences in the therapeutic effects between BMSC supernatant treated by nasal route and the conventional applications, i.e. intraperitoneal or intravenous injection.

conclusionsBMSC supernatant administered via the nasal cavity provide new sights and new ways for the EAE therapy.

Indexed as

Mesenchymal Stem Cell TransplantationAdministration, IntranasalAnimalsB-LymphocytesBrainDemyelinating DiseasesEncephalomyelitis, Autoimmune, ExperimentalFemaleInflammation MediatorsMesenchymal Stem CellsMice, Inbred C57BLSpinal CordT-LymphocytesInflammation MediatorsB cellsBMSCsEAENasal administration

Identifiers

PMID31730485
PMCPMC6858701
OpenAlexW2986367121

What OpenQuestion holds

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LicenceCC BY
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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.