Evidence map›Paper›PMID 18841093›Full record

ReviewMolecular therapy : the journal of the American Society of Gene Therapy2009

Herpes vector-mediated gene transfer in the treatment of chronic pain.

Joseph C Glorioso, David J Fink

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Molecular therapy : the journal of the American Society of Gene Therapy, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00804076 (Gene Transfer for Intractable Pain), which is not on this map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
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.

NCT00804076 phase1completednot on this map

Gene Transfer for Intractable Pain: A Phase I Clinical Trial to Determine the Maximum Tolerable Dose of a Replication-Defective Herpes Simplex Virus Type I (HSV-1) Vector Expressing Human Preproenkephalin (NP2) in Patients With Malignancies

TypeinterventionalSponsorDiamyd IncRan2008 to 2013Enrolled10ConditionsCancer PainArmsNP2
3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Review
  3. Gene therapy then and now: A look back at changes in the field over the past 25 years.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
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  5. Review
  6. Review
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  14. Gene therapy and peripheral nerve repair: a perspective.Frontiers in molecular neuroscience · 2015
    Article
  15. Article
  16. Review
  17. Review
  18. 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

2 authors at 2 institutions in 1 country.

Joseph C Glorioso1Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
David J Fink
University of Pittsburgh · USVA Ann Arbor Healthcare System · US

Funding

Vector delivery to modify the brain tumor and its microenvironmentP01NS040923 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GLORIOSO, JOSEPH C · 2002 to 2012
$12.7M
PRE-CLINICAL VECTOR PRODUCTIONP01DK044935 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GLORIOSO, JOSEPH C · 1993 to 2010
$11.8M
Preclinical Gene Therapy in a Large Animal Model of DMDU54AR050733 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GLORIOSO, JOSEPH C · 2003 to 2008
$7.7M
GENE TRANSFER FOR PREVENTION OF DIABETIC NEUROPATHYR01NS038850 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FINK, DAVID J. · 1999 to 2012
$3.3M
Glioma Therapy Using Targeted Oncolytic HSV VectorsR01CA119298 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GLORIOSO, JOSEPH C · 2006 to 2010
$1.8M
Sox11 and Functional Recovery of Sensory NeuronsR01NS059003 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ALBERS, KATHRYN MARIE · 2008 to 2012
$1.6M
NCI NIH HHS CA119298NCI NIH HHS R01 CA119298NIAMS NIH HHS U54 AR050733NIAMS NIH HHS U54AR050733NIDDK NIH HHS DK044935NIDDK NIH HHS P01 DK044935NINDS NIH HHS NS038850NINDS NIH HHS NS059003NINDS NIH HHS NS40923NINDS NIH HHS P01 NS040923NINDS NIH HHS R01 NS038850NINDS NIH HHS R01 NS059003
6 · The paper itself

Abstract

Chronic pain is a major health concern with up to 50% of patients finding little if any relief following traditional pharmacotherapy. This review describes the treatment of chronic pain using herpes simplex virus type 1 (HSV)-based vectors. HSV can be effectively used to deliver pain-modulating transgenes to sensory neurons in vivo following intradermal inoculation. The vector genome persists in peripheral nerve bodies in an episomal state and serves as a platform for expression of natural pain-relieving molecules that access endogenous antinociceptive circuitry. The vectors are mutated to prevent reactivation from latency or spread to the central nervous system. Dermatome selection for administration of HSV vectors provides targeted delivery of pain gene therapy to primary afferent neurons. This novel approach alleviates pain without systemic side effects or the induction of tolerance and can be used in combination with standard pain treatments.

Indexed as

Pain ManagementChronic DiseaseGenetic TherapyGenetic VectorsHerpesvirus 1, HumanHumans

Identifiers

PMID18841093
PMCPMC2613169
OpenAlexW2378042990

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.