HSV Amplicons in Gene Therapy

Niza Frenkel, Ronit Sarid

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

Abstract

Herpes simplex virus (HSV) amplicons are defective virus vectors capable of introducing amplified foreign genes into variable types of eukaryotic cells, such as fibroblasts, macrophages, glia, and neurons in different organisms including rodents, monkeys, and human (refs. 1–3; reviewed in ref. 4). The defective viruses follow their nondefective counterparts in the ability to infect mitotic, as well as postmitotic cells. This makes them potentially useful vectors for use in nondividing cells, such as in nerve cells. Available retrovirus vectors employed to date for gene therapy require cell division and therefore cannot be used to target neurons.
Original languageAmerican English
Title of host publicationHerpes Simplex Virus Protocols
EditorsS. Moira Brown, Alasdair R. MacLean
PublisherHumana Press
Pages227-235
StatePublished - 1998

Publication series

NameMethods in Molecular Medicine
Volume10

Fingerprint

Dive into the research topics of 'HSV Amplicons in Gene Therapy'. Together they form a unique fingerprint.

Cite this