Evidence map›Paper›PMID 28084640›Full record

ReviewJournal of neuroscience research2017

Diversity of immune cell types in multiple sclerosis and its animal model: Pathological and therapeutic implications.

Yun Cheng, Li Sun, Zhongxiang Xie, Xueli Fan, Qingqing Cao, Jinming Han, Jie Zhu, Tao Jin

Abstract readReview
In one paragraph

Review in Journal of neuroscience research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

21 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Loss of ADAP1/CentA1 Protects Against Autoimmune Demyelination.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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  5. 1,25(OH)International journal of molecular sciences · 2023
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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.

Yun ChengDepartment of Neurology and Neuroscience Center, First Hospital of Jilin University, Changchun, China.
Li SunDepartment of Neurology and Neuroscience Center, First Hospital of Jilin University, Changchun, China.
Zhongxiang XieDepartment of Neurology and Neuroscience Center, First Hospital of Jilin University, Changchun, China.
Xueli FanDepartment of Neurology and Neuroscience Center, First Hospital of Jilin University, Changchun, China.
Qingqing CaoDepartment of Neurology and Neuroscience Center, First Hospital of Jilin University, Changchun, China.
Jinming HanDepartment of Neurology and Neuroscience Center, First Hospital of Jilin University, Changchun, China.
Jie ZhuDepartment of Neurology and Neuroscience Center, First Hospital of Jilin University, Changchun, China.
Tao JinDepartment of Neurology and Neuroscience Center, First Hospital of Jilin University, Changchun, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is an inflammatory, demyelinating disease of the central nervous system with an autoimmune attack on the components of the myelin sheath and axons. The etiology of the disease remains largely unknown, but it is commonly acknowledged that the development of MS probably results from the interaction of environmental factors in conjunction with a genetic predisposition. Current therapeutic approaches can only ameliorate the clinical symptoms or reduce the frequency of relapse in MS. Most drugs used in this disease broadly suppress the functions of immune effector cells, which can result in serious side effects. Thus, new therapeutic methods resulting in greater efficacy and lower toxicity are needed. Toward this end, cell-based therapies are of increasing interest in the treatment of MS. Several immunoregulatory cell types, including regulatory T cells, regulatory B cells, M2 macrophages, tolerogenic dendritic cells, and stem cells, have been developed as novel therapeutic tools for the treatment of MS. In this Review, we summarize studies on the application of these cell populations for the treatment of MS and its animal model, experimental autoimmune encephalomyelitis, and call for further research on applications and mechanisms by which these cells act in the treatment of MS. © 2017 The Authors Journal of Neuroscience Research Published by Wiley Periodicals, Inc.

Indexed as

AnimalsEncephalomyelitis, Autoimmune, ExperimentalHumansMiceMultiple SclerosisB cellsEAEmacrophagemultiple sclerosisstem cellsT cellstolerogenic dendritic cells

Identifiers

PMID28084640
PMCPMC5573979

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.