Evidence map›Paper›PMID 26823763›Full record

ArticleInternational journal of clinical and experimental pathology2015

Development of an improved animal model of experimental autoimmune myositis.

Juan Kang, Hong-Ya Zhang, Guo-Dong Feng, Dong-Yun Feng, Hong-Ge Jia

Open access · greenAbstract readComparative Study
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  9. Expression of a constitutively active humanLife science alliance · 2019
    Article
  10. Interleukin-37 (IL-37) Suppresses Pertussis Toxin-Induced Inflammatory Myopathy in a Rat Model.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  11. Article
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

5 authors at 1 institution in 1 country.

Juan KangDepartment of Neurology, Xijing Hospital, The Fourth Military Medical University Xi'an, Shaanxi, China.
Hong-Ya ZhangDepartment of Neurology, Xijing Hospital, The Fourth Military Medical University Xi'an, Shaanxi, China.
Guo-Dong FengDepartment of Neurology, Xijing Hospital, The Fourth Military Medical University Xi'an, Shaanxi, China.
Dong-Yun FengDepartment of Neurology, Xijing Hospital, The Fourth Military Medical University Xi'an, Shaanxi, China.
Hong-Ge JiaDepartment of Neurology, Xijing Hospital, The Fourth Military Medical University Xi'an, Shaanxi, China.
Xijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple animal models of experimental autoimmune myositis (EAM) have been developed. However, these models vary greatly in the severity of disease and reproducibility. The goal of this study was to test whether vaccination twice with increased dose of rat myosin and pertussis toxin (PT) could induce EAM with severer disease in mice. BALB/c mice were injected with 1 mg rat myosin in 50% complete Freund's adjuvant (CFA) weekly for four times and one time of PT (EAM) or twice with 1.5 mg myosin in CFA and PT (M-EAM). In comparison with that in the CFA and PT injected controls, vaccination with rat myosin and injection PT significantly reduced the muscle strength and EMG duration, elevated serum creatine kinase levels, promoted inflammatory infiltration in the muscle tissues, leading to pathological changes in the muscle tissues, demonstrating to induce EAM. Interestingly, we found that vaccination twice with the high dose of myosin and PT prevented EAM-related gain in body weights and caused significantly less muscle strength in mice. More importantly, all of the mice receiving high dose of myosin and PT survived while 3 out of 16 mice with four times of low dose of myosin died. Finally, vaccination with high dose of myosin promoted CD4(+) and CD8(+) T cell infiltration in the muscle tissues and up-regulated MHC-I expression in the muscle tissues of mice. Hence, the new model of EAM is a time-saving, efficient and easily replicable tool for studying autoimmune myositis.

Indexed as

MyosinsPertussis ToxinAnimalsBiomarkersCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChemotaxis, LeukocyteCreatine Kinase, MM FormDisease ProgressionFemaleGuinea PigsMice, Inbred BALB CMuscle, SkeletalMuscle StrengthNervous System Autoimmune Disease, ExperimentalPhenotypeBiomarkersCreatine Kinase, MM FormMyosinsPertussis Toxinanimal modelsExperimental autoimmune myositis (EAM)idiopathic inflammatory myopathies (IIM)immunosuppressive

Identifiers

PMID26823763
PMCPMC4713549
OpenAlexW2416380622

What OpenQuestion holds

Textmetadata
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.