Oxophenarsine, an antisyphilis drug inhibits HIV-1-specific protein synthesis in acutely and persistently infected lymphocytes

  • AIDS Res Hum Retroviruses. 1990 Dec;6(12):1417-23. doi: 10.1089/aid.1990.6.1417.
P Gupta  1 R Balachandran P Thampatty C Rinaldo M Ho
Affiliations
  • 1. Department of Infectious Diseases and Microbiology, Graduate School of Public Health, University of Pittsburgh School of Medicine, PA.
Abstract

The development of drugs that can inhibit both acute and persistent anti-human immunodeficiency virus type 1 (HIV-1) Infection is a major goal in the treatment of patients with acquired immunodeficiency syndrome (AIDS). Most of the anti-HIV-1 drugs reported thus far, such as azidothymidine (AZT), inhibit acute HIV-1 Infection but have no Antiviral effect against persistent Infection. We report here that oxophenarsine (3-amino-4 hydroxyphenylarsineoxide hydrochloride), an antisyphilus drug inhibits HIV-1 production in acutely infected peripheral blood lymphocytes (PBL) and persistently infected T cells. In acutely infected PBL and H9 T cells, the drug is effective at concentrations as low as 0.07-0.15 micrograms/ml with no significant cytotoxicity at concentrations of 6.0 micrograms/ml or below. It does not inhibit HIV-1 Reverse Transcriptase at doses up to 60 micrograms/ml. The drug has no effect on HIV-1-specific DNA and RNA synthesis. However, it inhibits HIV-1 protein synthesis in both acutely and persistently infected cells.

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