Evidence map›Paper›PMID 29570934›Full record

ArticleJournal of cellular and molecular medicine2018

Non-erythropoietic erythropoietin-derived peptide protects mice from systemic lupus erythematosus.

Bo Huang, Juntao Jiang, Bangwei Luo, Wen Zhu, Yuqi Liu, Zhishang Wang, Zhiren Zhang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Roles of macrophages in lupus nephritis.Frontiers in pharmacology · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. 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

7 authors at 1 institution in 1 country.

Bo HuangInstitute of Immunology, Army Medical University, Chongqing, China.
Juntao JiangInstitute of Immunology, Army Medical University, Chongqing, China.
Bangwei LuoInstitute of Immunology, Army Medical University, Chongqing, China.
Wen ZhuInstitute of Immunology, Army Medical University, Chongqing, China.
Yuqi LiuInstitute of Immunology, Army Medical University, Chongqing, China.
Zhishang WangInstitute of Immunology, Army Medical University, Chongqing, China.
Zhiren ZhangInstitute of Immunology, Army Medical University, Chongqing, China.ORCID 0000-0002-5238-2835
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is an autoimmune disease, which results in various organ pathologies. However, current treatment towards SLE is suboptimal. Erythropoietin (EPO) has been shown to promote SLE recovery, but clinical application can be limited by its haematopoiesis-stimulating effects. EPO-derived helix-B peptide (ARA290) is non-erythrogenic but has been reported to retain the anti-inflammatory and tissue-protective functions of EPO. Therefore, here we investigated the effects and potential mechanisms of ARA290 on SLE. The administration of ARA290 to pristane-induced SLE and MRL/lpr mice significantly suppressed the level of serum antinuclear autoantibodies (ANAs) and anti-dsDNA autoantibodies, reduced the deposition of IgG and C3, and ameliorated the nephritis symptoms. Moreover, the serum concentrations of inflammatory cytokine IL-6, MCP-1 and TNF-α in SLE mice were reduced by ARA290. Further, ARA290 decreased the number of apoptotic cells in kidney. In vitro experiment revealed that ARA290 inhibited the inflammatory activation of macrophages and promoted the phagocytotic function of macrophages to apoptotic cells. Finally, ARA290 did not induce haematopoiesis during treatment. In conclusion, ARA290 ameliorated SLE, which at least could be partly due to its anti-inflammatory and apoptotic cell clearance promoting effects, without stimulating haematopoiesis, suggesting that ARA290 could be a hopeful candidate for SLE treatment.

Indexed as

AnimalsCytokinesDisease Models, AnimalErythropoietinFemaleHematopoiesisInflammationKidneyLupus Erythematosus, SystemicMacrophage ActivationMiceMice, Inbred C57BLMice, Inbred MRL lprOligopeptidesPhagocytosisRAW 264.7 CellscibinetideCytokinesErythropoietinOligopeptidespristaneTerpeneserythropoietininflammationmacrophagesystemic lupus erythematosus

Identifiers

PMID29570934
PMCPMC6010693
OpenAlexW2793109157

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.