Long-term Suppression of HIV-1 by Hydroxyurea and Didanosine
- 14 May 1997
- journal article
- research article
- Published by American Medical Association (AMA)
- Vol. 277 (18) , 1437-1438
- https://doi.org/10.1001/jama.1997.03540420033024
Abstract
To the Editor. —The use of hydroxyurea has been brought rapidly from laboratory studies to clinical implementation. After our initial demonstration of the potential use of hydroxyurea to inhibit human immunodeficiency virus (HIV)-1 replication,1other laboratories have shown that hydroxyurea and didanosine appear to be a powerful combination and lead to synergistic effects.2 In this study, 6 consecutive patients (Table) were treated with a combination of hydroxyurea (250-mg dose, 4 times per day) and didanosine (200-mg dose, 2 times per day). The group represented a heterogeneous population. Three patients had acquired immunodeficiency syndrome (AIDS), and 1 (patient 4) was enrolled following an episode of acute mononucleosis-like HIV syndrome 8 weeks after documented seroconversion. The response to treatment revealed a consistent pattern independent of previous exposure to antiretroviral treatment and disease stage. An initial sharp decrease in viremia (average, 84.5%) was observed in all patients 2 to 6 weeks afterKeywords
This publication has 2 references indexed in Scilit:
- Synergistic anti-human immunodeficiency virus type 1 effect of hydroxamate compounds with 2',3'-dideoxyinosine in infected resting human lymphocytes.Proceedings of the National Academy of Sciences, 1994
- Low levels of deoxynucleotides in peripheral blood lymphocytes: a strategy to inhibit human immunodeficiency virus type 1 replication.Proceedings of the National Academy of Sciences, 1993