Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Gene transfer to neurons using herpes simplex virus-based vectors

D J Fink1, N A DeLuca, W F Goins

  • 1Department of Neurology University of Pittsburgh, Pennsylvania 15261, USA.

Annual Review of Neuroscience
|January 1, 1996
PubMed
Summary

Herpes simplex virus type 1 (HSV-1) shows promise as a gene therapy vector for the nervous system. Researchers are developing safe and efficient HSV-1 vectors for direct in vivo gene transfer to neurons.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

A Novel Oncolytic Herpes Simplex Virus Design based on the Common Overexpression of microRNA-21 in Tumors.

Journal of gene therapy·2018
Same author

Rotational Energy as Mass in H_{3}^{+} and Lower Limits on the Atomic Masses of D and ^{3}He.

Physical review letters·2018
Same author

Effects of herpes simplex virus vectors encoding poreless TRPV1 or protein phosphatase 1α in a rat cystitis model induced by hydrogen peroxide.

Gene therapy·2017
Same author

Gene therapy-from small beginnings to where we are now.

Gene therapy·2017
Same author

MnSOD mediated by HSV vectors in the periaqueductal gray suppresses morphine withdrawal in rats.

Gene therapy·2017
Same author

Development of an oncolytic HSV vector fully retargeted specifically to cellular EpCAM for virus entry and cell-to-cell spread.

Gene therapy·2016

Area of Science:

  • Molecular Medicine
  • Neuroscience
  • Gene Therapy

Background:

  • Gene transfer technologies are crucial for molecular medicine and clinical practice.
  • Developing safe and efficient gene delivery vectors for specific tissues, especially postmitotic neurons, remains a challenge.
  • Herpes simplex virus type 1 (HSV-1) is a neurotropic virus that naturally infects neurons and establishes latency, suggesting its potential as a gene transfer vector.

Purpose of the Study:

  • To review the suitability of HSV-1 as a gene transfer vector for the nervous system.
  • To discuss strategies for modifying HSV-1 to reduce pathogenesis and enhance transgene expression.
  • To evaluate the efficiency and safety of HSV-1-based vectors in gene transfer experiments.

Main Methods:

  • Review of HSV-1 molecular biology.

Related Experiment Videos

  • Description of strategies for recombinant vector safety enhancement.
  • Methods for expressing transgenes from engineered HSV-1 genomes.
  • Evaluation of gene transfer experiments using recombinant and amplicon HSV-1 vectors.
  • Main Results:

    • HSV-1 possesses unique characteristics making it a viable candidate for neural gene delivery.
    • Recombinant and defective HSV-1 vectors have been developed and tested for gene transfer.
    • The efficiency and safety of these HSV-1-based vectors in gene transfer applications have been assessed.

    Conclusions:

    • HSV-1-based vectors offer a promising approach for gene therapy in the nervous system.
    • Further development is needed to optimize safety and efficiency for clinical applications.
    • HSV-1 vectors hold potential for revolutionizing experimental neuroscience and clinical medicine.