Lamivudine or stavudine in two- and three-drug combinations against human immunodeficiency virus type 1 replication in vitro
- PMID: 8568296
- DOI: 10.1093/infdis/173.2.355
Lamivudine or stavudine in two- and three-drug combinations against human immunodeficiency virus type 1 replication in vitro
Abstract
Two- and three-drug combinations of lamivudine or stavudine with other antiretroviral drugs were evaluated for activity against human immunodeficiency virus type 1 (HIV-1) activity in peripheral blood mononuclear cells. Other agents included zidovudine, didanosine, nevirapine, and saquinavir. Paired zidovudine-sensitive and -resistant clinical HIV-1 isolates were used. Additive or synergistic interactions were observed against the zidovudine-sensitive isolate with the following combinations: lamivudine-zidovudine, lamivudine-stavudine, lamivudine-saquinavir, lamivudine-nevirapine, stavudine-zidovudine, stavudine-didanosine, stavudine-saquinavir, stavudine-nevirapine, lamivudine-zidovudine-saquinavir, lamivudine-zidovudine-stavudine, stavudine-zidovudine-nevirapine, lamivudine-zidovudine-nevirapine, and stavudine-zidovudine-saquinavir. Against the zidovudine-resistant isolate, additive or synergistic interactions were seen with most two- and three-drug combinations, but the combination of stavudine-zidovudine was antagonistic. The clinical implications of these in vitro observations should be explored.
Similar articles
-
The M184V mutation in HIV-1 reverse transcriptase (RT) conferring lamivudine resistance does not result in broad cross-resistance to nucleoside analogue RT inhibitors.AIDS. 1998 May 7;12(7):705-12. doi: 10.1097/00002030-199807000-00006. AIDS. 1998. PMID: 9619801
-
In vitro anti-HIV potency of stampidine alone and in combination with standard anti-HIV drugs.Arzneimittelforschung. 2005;55(4):223-31. doi: 10.1055/s-0031-1296849. Arzneimittelforschung. 2005. PMID: 15901046
-
In vitro comparison of selected triple-drug combinations for suppression of HIV-1 replication: the Inter-Company Collaboration Protocol.J Acquir Immune Defic Syndr Hum Retrovirol. 1995;10 Suppl 2:S83-91. J Acquir Immune Defic Syndr Hum Retrovirol. 1995. PMID: 7552518
-
Prevalence and incidence of resistance to zidovudine and other antiretroviral drugs.Am J Med. 1997 May 19;102(5B):70-5. doi: 10.1016/s0002-9343(97)00067-3. Am J Med. 1997. PMID: 9845501 Review.
-
Didanosine: an updated review of its use in HIV infection.Drugs. 1999 Dec;58(6):1099-135. doi: 10.2165/00003495-199958060-00009. Drugs. 1999. PMID: 10651392 Review.
Cited by
-
Population pharmacokinetics of nevirapine, zidovudine, and didanosine in human immunodeficiency virus-infected patients. The National Institute of Allergy and Infectious Diseases AIDS Clinical Trials Group Protocol 241 Investigators.Antimicrob Agents Chemother. 1999 Jan;43(1):121-8. doi: 10.1128/AAC.43.1.121. Antimicrob Agents Chemother. 1999. PMID: 9869576 Free PMC article. Clinical Trial.
-
Nevirapine: a review of its use in the prevention and treatment of paediatric HIV infection.Paediatr Drugs. 2000 Sep-Oct;2(5):373-407. doi: 10.2165/00128072-200002050-00005. Paediatr Drugs. 2000. PMID: 11022799 Review.
-
Lamivudine. A review of its antiviral activity, pharmacokinetic properties and therapeutic efficacy in the management of HIV infection.Drugs. 1997 Apr;53(4):657-80. doi: 10.2165/00003495-199753040-00008. Drugs. 1997. PMID: 9098665 Review.
-
Activities of the human immunodeficiency virus type 1 (HIV-1) protease inhibitor nelfinavir mesylate in combination with reverse transcriptase and protease inhibitors against acute HIV-1 infection in vitro.Antimicrob Agents Chemother. 1997 Oct;41(10):2159-64. doi: 10.1128/AAC.41.10.2159. Antimicrob Agents Chemother. 1997. PMID: 9333041 Free PMC article.
-
Interferon alpha antagonizes the anti-hepatoma activity of the oncolytic virus M1 by stimulating anti-viral immunity.Oncotarget. 2017 Apr 11;8(15):24694-24705. doi: 10.18632/oncotarget.15788. Oncotarget. 2017. PMID: 28445966 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources