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Dideoxynucleosides are less inhibitory in vitro against human immunodeficiency virus type 2 (HIV-2) than against HIV-1.

Abstract
The antiviral activities of various dideoxynucleosides against LAV strains of human immunodeficiency viruses type 1 (HIV-1) and type 2 (HIV-2) were evaluated. Significantly more 3'-azido-3'-deoxythymidine was required to inhibit the replication of HIV-2 than HIV-1 in three human cell lines. HIV-2 also appeared more resistant than HIV-1 to other dideoxynucleosides. These results suggest that dideoxynucleosides may be less effective in vivo for HIV-2 infection and that a broader range of clinical isolates of human retroviruses should be examined for drug susceptibility in vitro.
AuthorsD D Richman
JournalAntimicrobial agents and chemotherapy (Antimicrob Agents Chemother) Vol. 31 Issue 12 Pg. 1879-81 (Dec 1987) ISSN: 0066-4804 [Print] UNITED STATES
PMID3501941 (Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antiviral Agents
  • Zidovudine
  • Thymidine
Topics
  • Antiviral Agents (pharmacology)
  • Cell Line
  • Drug Resistance, Microbial
  • HIV (drug effects, physiology)
  • Humans
  • T-Lymphocytes (drug effects)
  • Thymidine (analogs & derivatives, pharmacology)
  • Virus Replication (drug effects)
  • Zidovudine

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