Evidence map›Paper›PMID 24603865›Full record

ArticlePloS one2014

Erythropoietin-derived nonerythropoietic peptide ameliorates experimental autoimmune neuritis by inflammation suppression and tissue protection.

Yuqi Liu, Bangwei Luo, Fuyu Han, Xiaoming Li, Jian Xiong, Man Jiang, Xioafeng Yang, Yuzhang Wu, Zhiren Zhang

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Painful Diabetic Peripheral Neuropathy: Practical Guidance and Challenges for Clinical Management.Diabetes, metabolic syndrome and obesity : targets and therapy · 2023
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
4 · The record

Corrections and comments

  • Erratum issued
    Dosage error in article text
5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Yuqi LiuInstitute of Immunology, Third Military Medical University of People's Liberation Army, Chongqing, China.
Bangwei LuoInstitute of Immunology, Third Military Medical University of People's Liberation Army, Chongqing, China.
Fuyu HanInstitute of Immunology, Third Military Medical University of People's Liberation Army, Chongqing, China.
Xiaoming LiInstitute of Immunology, Third Military Medical University of People's Liberation Army, Chongqing, China.
Jian XiongInstitute of Immunology, Third Military Medical University of People's Liberation Army, Chongqing, China.
Man JiangInstitute of Immunology, Third Military Medical University of People's Liberation Army, Chongqing, China.
Xioafeng YangInstitute of Immunology, Third Military Medical University of People's Liberation Army, Chongqing, China.
Yuzhang WuInstitute of Immunology, Third Military Medical University of People's Liberation Army, Chongqing, China.
Zhiren ZhangInstitute of Immunology, Third Military Medical University of People's Liberation Army, Chongqing, China.
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Experimental autoimmune neuritis (EAN) is an autoantigen-specific T-cell-mediated disease model for human demyelinating inflammatory disease of the peripheral nervous system. Erythropoietin (EPO) has been known to promote EAN recovery but its haematopoiesis stimulating effects may limit its clinic application. Here we investigated the effects and potential mechanisms of an EPO-derived nonerythropoietic peptide, ARA 290, in EAN. Exogenous ARA 290 intervention greatly improved EAN recovery, improved nerve regeneration and remyelination, and suppressed nerve inflammation. Furthermore, haematopoiesis was not induced by ARA 290 during EAN treatment. ARA 290 intervention suppressed lymphocyte proliferation and altered helper T cell differentiation by inducing increase of Foxp3+/CD4+ regulatory T cells and IL-4+/CD4+ Th2 cells and decrease of IFN-γ+/CD4+ Th1 cells in EAN. In addition, ARA 290 inhibited inflammatory macrophage activation and promoted its phagocytic activity. In vitro, ARA 290 was shown to promote Schwann cell proliferation and inhibit its inflammatory activation. In summary, our data demonstrated that ARA 290 could effectively suppress EAN by attenuating inflammation and exerting direct cell protection, indicating that ARA 290 could be a potent candidate for treatment of autoimmune neuropathies.

Indexed as

AnimalsCell DifferentiationCell ProliferationErythropoietinInflammationInjections, IntraperitonealInjections, SubcutaneousMaleNerve RegenerationNeuritis, Autoimmune, ExperimentalNeuropeptidesNeuroprotective AgentsOligopeptidesRatsRats, Inbred LewSciatic NervecibinetideErythropoietinNeuropeptidesNeuroprotective AgentsOligopeptides

Identifiers

PMID24603865
PMCPMC3946253
OpenAlexW2034368875

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.