Relay-Version: version B 2.10 5/3/83; site utzoo.UUCP Posting-Version: version B 2.10.2 9/18/84; site bbncc5.UUCP Path: utzoo!watmath!clyde!cbosgd!ihnp4!qantel!dual!lll-crg!seismo!harvard!bbnccv!bbncc5!sdyer From: sdyer@bbncc5.UUCP (Steve Dyer) Newsgroups: net.bio Subject: Re: anti RNA reverse transcriptase as HTLV therapy Message-ID: <622@bbncc5.UUCP> Date: Wed, 9-Oct-85 10:09:28 EDT Article-I.D.: bbncc5.622 Posted: Wed Oct 9 10:09:28 1985 Date-Received: Sat, 12-Oct-85 19:33:50 EDT References: <17@mit-amt.MIT.EDU> Organization: Bolt Beranek and Newman, Cambridge, MA Lines: 21 > Can someone say whether a human needs to have any RNA > reverse-transciptase? If not, could one not design an enzyme specially > made to disable it, and inhibit HTLV by placing large amounts of said > enzyme in one's body? I suppose you'd need to have some "friendly" > infectious organism in order to synthesize the quantities needed. Is > recombinant technology anywhere near able to do this? A number of new drugs (and some old ones--e.g., suramin, long used in the treatment of trypanosomiasis) inhibit RNA reverse-transscriptase and are presently undergoing clinical trials. Enzymes aren't necessarily needed; lots of simple (well, simple compared to enzymes) compounds bind to enzymes and render them inactive. One problem with such treatments, at least at the stage of the disease where they are being administered now, is that although HTLV-III might no longer be isolated from the patient, the T-cell situation does not seem to improve. -- /Steve Dyer {harvard,seismo}!bbnccv!bbncc5!sdyer sdyer@bbncc5.ARPA