Evidence map›Paper›PMID 20224990›Full record

ArticlePharmaceutical research2010

Release of plasmid DNA-encoding IL-10 from PLGA microparticles facilitates long-term reversal of neuropathic pain following a single intrathecal administration.

Ryan Gene Soderquist, Evan M Sloane, Lisa C Loram, Jacqueline A Harrison, Ellen C Dengler, Scott M Johnson, Luke D Amer, Courtney S Young, Makenzie T Lewis, Stephen Poole and 4 more

Open access · greenAbstract read
In one paragraph

Article in Pharmaceutical research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 89 citations in OpenAlex.

  1. Intrathecal drug delivery in the era of nanomedicine.Advanced drug delivery reviews · 2020
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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

14 authors at 3 institutions in 2 countries.

Ryan Gene SoderquistDepartment of Chemical & Biological Engineering, University of Colorado at Boulder, 424 UCB, Boulder, Colorado, 80309, USA.
Evan M Sloane
Lisa C Loram
Jacqueline A Harrison
Ellen C Dengler
Scott M Johnson
Luke D Amer
Courtney S Young
Makenzie T Lewis
Stephen Poole
Matthew G Frank
Linda R Watkins
Erin D Milligan
Melissa J Mahoney
University of Colorado Boulder · USUniversity of New Mexico · USNational Institute for Biological Standards and Control · GB

Funding

Spinal Neuroimmune Mechanisms Underlying IL-10 Gene Therapy for Pain ControlR01DA018156 · NIDA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI MILLIGAN, ERIN DAMITA · 2004 to 2014
$3.3M
LEADERSHIP TRAINING IN PHARMACEUTICAL BIOTECHNOLOGYT32GM008732 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI RANDOLPH, THEODORE W · 2001 to 2015
$2.7M
NIDA NIH HHS DA018156NIDA NIH HHS R01 DA018156NIGMS NIH HHS T32 GM008732
6 · The paper itself

Abstract

purposeInterleukin-10 (IL-10) is an anti-inflammatory molecule that has achieved interest as a therapeutic for neuropathic pain. In this work, the potential of plasmid DNA-encoding IL-10 (pDNA-IL-10) slowly released from biodegradable microparticles to provide long-term pain relief in an animal model of neuropathic pain was investigated.

methodsPLGA microparticles encapsulating pDNA-IL-10 were developed and assessed both in vitro and in vivo.

resultsIn vitro, pDNA containing microparticles activated macrophages, enhanced the production of nitric oxide, and increased the production of IL-10 protein relative to levels achieved with unencapsulated pDNA-IL-10. In vivo, intrathecally administered microparticles embedded in meningeal tissue, induced phagocytic cell recruitment to the cerebrospinal fluid, and relieved neuropathic pain for greater than 74 days following a single intrathecal administration, a feat not achieved with unencapsulated pDNA. Therapeutic effects of microparticle-delivered pDNA-IL-10 were blocked in the presence of IL-10-neutralizing antibody, and elevated levels of plasmid-derived IL-10 were detected in tissues for a prolonged time period post-injection (>28 days), demonstrating that therapeutic effects are dependent on IL-10 protein production.

conclusionsThese studies demonstrate that microparticle encapsulation significantly enhances the potency of intrathecally administered pDNA, which may be extended to treat other disorders that require intrathecal gene therapy.

Indexed as

Gene Transfer TechniquesAnimalsBehavior, AnimalCells, CulturedDNAGenetic TherapyImmunohistochemistryInjections, SpinalInterleukin-10Lactic AcidMacrophagesMaleNanoparticlesNitric OxideParticle SizePeripheral Nervous System DiseasesDNAInterleukin-10Lactic AcidNitric OxidePolyglycolic AcidPolylactic Acid-Polyglycolic Acid Copolymer

Identifiers

PMID20224990
PMCPMC3583569
OpenAlexW1981233223

What OpenQuestion holds

Textmetadata
LicenceTDM
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.