Seattle Treatment Education Project: STEP Perspective - Volume 4, Number 3 - October 1992
Lori Panther, M.D.
An effective form of protease inhibitor, Abbott 80987, was found to be active against HIV-infected cells in the laboratory, and oral absorption was good as measured in laboratory animals (Norbeck, USA, ThA1507). Another protease inhibitor, U-75875 (Upjohn) was found to be effective in suppression of HIV replication in chronically infected cells called macrophages; these cells serve as a reservoir of HIV (Perno, USA, ThA15604). However, one group found certain laboratory-adapted strains of HIV which were resistant to protease inhibitors (Patterson, USA, ThA1506).
Preliminary findings on new agents. Several new compounds with anti-HIV activity tested only in the laboratory were reported. Quinobene, a sulfonated dye compound, was found to be effective against HIV-1 and HIV-2 as well as AZT-resistant isolates (Bader, USA, PoA2297). BRL 47923 is a nucleoside RT inhibitor found to have in vitro anti-HIV activity (Kenig,UK,PoA2311). A sulfated derivative of a drug called chitosan has been found to have similar properties (Kornilaveva, Russia, PoA2312). Another non- nucleoside RT inhibitor from a class of drugs called thiazolo-iso- indolinones (the compound tested was numbered BM21.1298) was noted to be effective against HIV-1 only (Maas, Germany, PoA2314). An in vitro study of the immunotherapeutic agent RFT5-dgA, which is selectively toxic for HIV-infected CD4 cells, showed suppression of viral production in HIV-infected cell culture (Bell, USA, PoB3438).
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