Evidence map›Paper›PMID 26271954›Full record

ReviewNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2015

A Distinct Region in Erythropoietin that Induces Immuno/Inflammatory Modulation and Tissue Protection.

RuiRong Yuan, Bo Wang, Wei Lu, Yasuhiro Maeda, Peter Dowling

Open access · bronzeAbstract readReview
In one paragraph

Review in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Frontiers in aging neuroscience · 2019
    Article
  15. Review
  16. Article
  17. Article
  18. Erythropoietin Pathway: A Potential Target for the Treatment of Depression.International journal of molecular sciences · 2016
    Review
  19. Beneficial Effect of Erythropoietin Short Peptide on Acute Traumatic Brain Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2016
    Article
  20. 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 2 institutions in 1 country.

RuiRong YuanNeurology Service, VA Medical Center of East Orange, East Orange, NJ, USA.
Bo WangNeurology Service, VA Medical Center of East Orange, East Orange, NJ, USA.
Wei LuNeurology Service, VA Medical Center of East Orange, East Orange, NJ, USA.
Yasuhiro MaedaNeurology Service, VA Medical Center of East Orange, East Orange, NJ, USA.
Peter DowlingNeurology Service, VA Medical Center of East Orange, East Orange, NJ, USA. dowlinpc@njms.rutgers.edu.
Rutgers, The State University of New Jersey · USEast Orange VA Medical Center · US

Funding

New generation EPO peptides with enhanced safety for acute TBII01RX000220 · VA · VA NEW JERSEY HEALTH CARE SYSTEM · PI DOWLING, PETER C · 2009 to 2015
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Novel EPO peptide therapy for a new mouse model of dementiaI01RX001305 · VA · VA NEW JERSEY HEALTH CARE SYSTEM · PI DOWLING, PETER C · 2015 to 2019
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NINDS NIH HHS 1 X01 NS0073526-01A1RRD VA I01 RX000220RRD VA I01 RX001305
6 · The paper itself

Abstract

Beneficial effects of short-term whole-molecule erythropoietin (EPO) therapy have been demonstrated on several animal models of diverse central nervous system pathology. However, the increased hematocrit induced by EPO-driven marrow stimulation greatly limits its potential for side effect-free therapy. We created a library of EPO-derived fragments based on the hypothesis that 2 distinct functions, erythropoiesis and tissue protection, reside in different regions of the molecule. Several small EPO-derived peptides within the Aβ loop of whole EPO molecule were screened for tissue protection in EAE mice. The 19-mer JM-4 peptide that contains 2 cysteine molecules consistently demonstrated the most potent clinical beneficial effects without producing hematocrit alterations in animal models of EAE. The JM-4-induced tissue protection was associated with modulation of the immunoregulatory process that drives inflammation and provokes subsequent autoimmune damage. Like the whole EPO molecule, JM-4 effectively modulated immune/inflammatory reaction within both the peripheral lymphatic tissue and central nervous system. The major effects induced by JM-4 include blocked expansion of monocyte/dendritic antigen presenting cell and T helper 17 cell populations, decreased proinflammatory cytokine production, and sharply enhanced expansion of the regulatory T-cell population. JM-4 shows promise for treatment of a broad spectrum of neural and non-neural conditions associated with inflammation.

Indexed as

AnimalsAnti-Inflammatory AgentsApoptosisCytokinesDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalErythropoietinHumansLymph NodesLymphocytesMice, Inbred C57BLPC12 CellsRatsSpinal CordAnti-Inflammatory AgentsCytokinesErythropoietinErythropoietinExperimental autoimmune encephalomyelitisImmunomodulationMultiple sclerosisPeptide

Identifiers

PMID26271954
PMCPMC4604189
OpenAlexW1464504309

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.