Molecular targets for interference with viral replication. NLM AIDSLINE Important note: Information in this article was accurate in 1993. The state of the art may have changed since the publication date.

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Molecular targets for interference with viral replication.

Int Conf AIDS. 1993 Jun 6-11;9(1):10 (abstract no. PS-03-1). Unique Identifier : AIDSLINE MED/93333217
Wong-Staal F; Dept. of Medicine, UCSD, La Jolla 92093.


Abstract: Therapeutic intervention of HIV-1 replication can be achieved by interfering with key steps in the virus life cycle, including entry, reverse transcription, transcription, translation, packaging, and virus release. In addition, inhibition of the early, essential regulatory genes, tat and rev, would pre-empt possibility of virus production and spread. Tat and Rev directly bind to their respective RNA targets, TAR and RRE. Cellular proteins also bind to these viral proteins and RNA elements. These components form large functional complexes, the disruption of which should halt virus production. The use of RNA decoys, transdominant proteins and anti-sense/catalytic RNAs all aim at interfering such complex formation. As the technology of gene therapy is refined, the prospects of treatment of AIDS using these approaches would also improve. Finally, the vif, nef, vpu/vpx and vpr genes are also potential targets as they contribute to replication efficiency and pathogenicity in vivo.
Keywords: *Acquired Immunodeficiency Syndrome/THERAPY *HIV-1/PHYSIOLOGY *Virus ReplicationKWDacquiredimmunodeficiencysyndrome/therapyKWDhiv-1/physiologyKWDvirusreplication
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Copyright © 1993 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

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