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Inhibitory effect of 2',3'-didehydro-2',3'-dideoxynucleosides on infectivity, cytopathic effects, and replication of human immunodeficiency virus.

Abstract
It is generally accepted that human immunodeficiency virus (HIV) is the etiologic agent of the acquired immunodeficiency syndrome and related diseases. In this report, we demonstrate the antiviral effect of nucleoside analogs 2',3'-didehydro-2',3'-dideoxythymidine (DHT) and 2',3'-didehydro-2',3'-dideoxycytidine (DHC) by using human T-cell lymphotropic virus type I-carrying MT-4 cells, which are extremely susceptible to HIV infection. These agents efficiently inhibited the cytopathic effects and expression of HIV-specific antigens in MT-4 cells after infection of the virus. Both DHT and DHC also strongly blocked viral replication as determined by our quantitative bioassay system using a plaque-forming assay. These antiviral effects were obtained at concentrations at which the drugs produced little or no toxicity and were comparable to those with 3'-azido-3'-deoxythymidine and 2',3'-dideoxynucleosides. These findings warrant further investigation of the use of DHT and DHC for the treatment of the acquired immunodeficiency syndrome and related diseases.
AuthorsY Hamamoto, H Nakashima, T Matsui, A Matsuda, T Ueda, N Yamamoto
JournalAntimicrobial agents and chemotherapy (Antimicrob Agents Chemother) Vol. 31 Issue 6 Pg. 907-10 (Jun 1987) ISSN: 0066-4804 [Print] United States
PMID3039911 (Publication Type: Journal Article)
Chemical References
  • Antigens, Viral
  • Antiviral Agents
  • Dideoxynucleosides
  • 2',3'-dideoxythymidine
  • Zidovudine
  • Zalcitabine
  • Stavudine
  • 2',3'-dideoxycytidinene
  • Thymidine
Topics
  • Antigens, Viral (immunology)
  • Antiviral Agents (pharmacology)
  • Cells, Cultured
  • Cytopathogenic Effect, Viral (drug effects)
  • Dideoxynucleosides
  • HIV (drug effects, immunology, pathogenicity)
  • Humans
  • Stavudine
  • Thymidine (analogs & derivatives, pharmacology)
  • Viral Plaque Assay
  • Virus Replication (drug effects)
  • Zalcitabine (analogs & derivatives, pharmacology)
  • Zidovudine

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