Evidence map›Paper›PMID 19262611›Full record

ReviewGene therapy2009

Long-term control of neuropathic pain in a non-viral gene therapy paradigm.

E M Sloane, R G Soderquist, S F Maier, M J Mahoney, L R Watkins, E D Milligan

Open access · bronzeAbstract readReview
In one paragraph

Review in Gene therapy, 2009. 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
1.4field-weighted citation impact, top 24% 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, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Neuroimmune modulation of pain and regenerative pain medicine.The Journal of clinical investigation · 2020
    Review
  5. Article
  6. Article
  7. AAV-Mediated Gene Transfer to Dorsal Root Ganglion.Methods in molecular biology (Clifton, N.J.) · 2016
    Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Mesoporous silica-supported lipid bilayers (protocells) for DNA cargo delivery to the spinal cord.Journal of controlled release : official journal of the Controlled Release Society · 2013
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

6 authors at 2 institutions in 1 country.

E M SloaneDepartment of Psychology and Center for Neuroscience, University of Colorado, Boulder, CO, USA.
R G Soderquist
S F Maier
M J Mahoney
L R Watkins
E D Milligan
University of Colorado Boulder · USUniversity of New Mexico · US

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
Immune and Gilia Regulation of Pain & Analgesic ActionsK05DA024044 · NIDA · UNIVERSITY OF COLORADO · PI WATKINS, LINDA · 2008 to 2012
$616k
Immune/Glial Mediation of Exaggerated Pain StatesK02DA015642 · NIDA · UNIVERSITY OF COLORADO AT BOULDER · PI WATKINS, LINDA · 2003 to 2007
$600k
Pain control via spinal interleukin-10 gene therapyR21DA015656 · NIDA · UNIVERSITY OF COLORADO AT BOULDER · PI WATKINS, LINDA · 2002 to 2003
$296k
NIDA NIH HHS DA015642NIDA NIH HHS DA015656NIDA NIH HHS DA018156NIDA NIH HHS DA024044NIDA NIH HHS K02 DA015642NIDA NIH HHS K05 DA024044NIDA NIH HHS R01 DA018156NIDA NIH HHS R21 DA015656NIGMS NIH HHS T32 GM008732
6 · The paper itself

Abstract

Traditional approaches to treating chronic neuropathic pain largely focus on manipulations directly altering neuronal activity or neuron-to-neuron communication. Recently, however, it has become clear that glial cells (including microglia and astroglia) play a significant role in pain expression in a variety of neuropathic pain models. Multiple aspects of the inflammatory response of glial cells, commonly observed in neuropathic pain conditions, have been implicated in pain expression. Thus, glial cell inflammation has emerged as a potential therapeutic target in neuropathic pain. Our laboratory has been exploring the use of an anti-inflammatory cytokine, interleukin-10 (IL-10), to control glial inflammatory activation thereby controlling neuropathic pain. IL-10 protein delivery is limited by a short half-life and an inability to cross into the central nervous system from the periphery, making a centrally delivered gene therapy approach attractive. We have recently characterized a non-viral gene therapy approach using two injections of naked DNA to achieve long-term (>3 months) control of neuropathic pain in a peripheral nerve injury model. Timing and dose requirements leading to long-term pain control are discussed in this review, as is recent work using microparticle-encapsulated DNA to achieve long-term therapeutic efficacy with a single injection.

Indexed as

Pain ManagementAnimalsChronic DiseaseDNAGenetic TherapyGene Transfer TechniquesInterleukin-10NeurogliaDNAInterleukin-10

Identifiers

PMID19262611
PMCPMC2756299
OpenAlexW1991900761

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.