Evidence map›Paper›PMID 24433027›Full record

ArticleMolecular pharmaceutics2014

Treatment of experimental autoimmune encephalomyelitis by codelivery of disease associated Peptide and dexamethasone in acetalated dextran microparticles.

Kevin J Peine, Mireia Guerau-de-Arellano, Priscilla Lee, Naveen Kanthamneni, Mary Severin, G Duane Probst, Haiyan Peng, Yuhong Yang, Zachary Vangundy, Tracey L Papenfuss and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 72 citations in OpenAlex.

  1. Review
  2. Article
  3. Multiple sclerosis: molecular pathogenesis and therapeutic intervention.Signal transduction and targeted therapy · 2025
    Review
  4. Harnessing mRNA-lipid nanoparticles as innovative therapies for autoimmune diseases.Molecular therapy. Methods & clinical development · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Vaccines for immune tolerance against autoimmune disease.Advanced drug delivery reviews · 2023
    Review
  12. Review
  13. A predictive mechanistic model of drug release from surface eroding polymeric nanoparticles.Journal of controlled release : official journal of the Controlled Release Society · 2022
    Article
  14. Review
  15. Review
  16. Review
  17. PEGylation enables subcutaneously administered nanoparticles to induce antigen-specific immune tolerance.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Article
  18. Review
  19. Article
  20. Review
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

13 authors at 2 institutions in 1 country.

Kevin J PeineMolecular, Cellular and Developmental Biology Graduate Program, The Ohio State University , Columbus, Ohio, 43210, United States.
Mireia Guerau-de-Arellano
Priscilla Lee
Naveen Kanthamneni
Mary Severin
G Duane Probst
Haiyan Peng
Yuhong Yang
Zachary Vangundy
Tracey L Papenfuss
Amy E Lovett-Racke
Eric M Bachelder
Kristy M Ainslie
The Ohio State University · USThe Ohio State University Wexner Medical Center · US

Funding

Encapsulated Active Vitamin D Vaccine for the Treatment of Multiple SclerosisR21NS072813 · NINDS · OHIO STATE UNIVERSITY · PI AINSLIE, KRISTY M · 2011 to 2012
$419k
NINDS NIH HHS NIH R21 NS072813-01NINDS NIH HHS R21 NS072813
6 · The paper itself

Abstract

Multiple sclerosis (MS) is an autoimmune, demyelinating disease of the central nervous system that can cause loss of motor function and is thought to result, in part, from chronic inflammation due to an antigen-specific T cell immune response. Current treatments suppress the immune system without antigen specificity, increasing the risks of cancer, chronic infection, and other long-term side effects. In this study, we show treatment of experimental autoimmune encephalomyelitis (EAE), a model of MS, by coencapsulating the immunodominant peptide of myelin oligodendrocyte glycoprotein (MOG) with dexamethasone (DXM) into acetalated dextran (Ac-DEX) microparticles (DXM/MOG/MPs) and administering the microparticles subcutaneously. The clinical score of the mice was reduced from 3.4 to 1.6 after 3 injections 3 days apart with the coencapsulated microparticulate formulation (MOG 17.6 μg and DXM 8 μg). This change in clinical score was significantly greater than observed with phosphate-buffered saline (PBS), empty MPs, free DXM and MOG, DXM/MPs, and MOG/MPs. Additionally, treatment with DXM/MOG/MPs significantly inhibited disease-associated cytokine (e.g., IL-17, GM-CSF) expression in splenocytes isolated in treated mice. Here we show a promising approach for the therapeutic treatment of MS using a polymer-based microparticle delivery platform.

Indexed as

Drug Delivery SystemsAnimalsCell ProliferationCombined Modality TherapyCytokinesDexamethasoneDextransEncephalomyelitis, Autoimmune, ExperimentalFemaleFlow CytometryMiceMice, Inbred C57BLMyelin-Oligodendrocyte GlycoproteinNitric OxidePeptide FragmentsPolymersCytokinesDexamethasoneDextransMog protein, mouseMyelin-Oligodendrocyte GlycoproteinNitric OxidePeptide FragmentsPolymers

Identifiers

PMID24433027
PMCPMC3993881
OpenAlexW2080753451

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.