Mutagenic outcome of combined antiviral drug treatment during human immunodeficiency virus type 1 replication

被引:24
作者
Mansky, LM
机构
[1] Ohio State Univ, Med Ctr, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[2] Ohio State Univ, Med Ctr, Ctr Comprehens Canc, Columbus, OH 43210 USA
[3] Ohio State Univ, Med Ctr, Ctr Retrovirus Res, Columbus, OH 43210 USA
关键词
nucleoside; polymerase; evolution; drug; mutagenesis;
D O I
10.1016/S0042-6822(02)00069-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The development of antiviral drug resistance is an important problem in the treatment of human immunodeficiency virus type 1 (HIV-1) infection. Potent antiretroviral therapy (ART) is currently used for treatment, and typically consists of at least two reverse transcriptase (RT) inhibitors. To assess the impact of combination therapy on HIV-1 mutagenesis, the mutagenic outcome of combined drug treatment was determined with several different RT drug combinations. Significant increases in HIV-1 mutant frequencies were observed with combinations of nucleoside RT inhibitors as well as in combinations where nucleoside inhibitors were used along with hydroxyurea, a drug known to deplete nucleotide pools in cells. This indicates that combinations of RT drugs can act together to further increase HIV-1 mutant frequencies, which could have important implications for virus population dynamics and could compromise drug therapy regimens. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:116 / 121
页数:6
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