Mechanisms of early virologic failure in antiretroviral-naive patients starting protease inhibitor-containing regimens:: The APROVIR study

被引:25
|
作者
Masquelier, B
Peytavin, G
Leport, C
Droz, C
Duran, S
Verdon, R
Besnier, JM
Chêne, G
Raffi, F
Brun-Vézinet, F
机构
[1] CHU Bordeaux, Hop Pellegrin, Virol Lab, F-33076 Bordeaux, France
[2] Univ Bordeaux 2, INSERM, U330, F-33076 Bordeaux, France
[3] Hop Bichat Claude Bernard, Pharmacol Lab, F-75877 Paris, France
[4] Hop Bichat Claude Bernard, Serv Malad Infect & Trop, F-75877 Paris 18, France
[5] Hop Bichat Claude Bernard, Virol Lab, F-75877 Paris 18, France
[6] INSERM, U379, F-13258 Marseille, France
[7] CHU Cote Nacre, Serv Malad Infect, Caen, France
[8] Hop Bretonneau, Serv Malad Infect, Tours, France
[9] Hotel Dieu Nantes, Serv Malad Infect & Trop, Nantes, France
来源
JOURNAL OF INFECTIOUS DISEASES | 2002年 / 186卷 / 10期
关键词
D O I
10.1086/344358
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The virologic and pharmacologic mechanisms of virologic failure (VF) were studied in 243 antiretroviral-naive patients starting first-line protease inhibitor (PI)-containing therapy (nelfinavir in 66% and indinavir in 19%). Among the 220 patients with follow-up data, VF occurred in 35 (16%) during the first year of follow-up. A higher baseline virus load and poorer adherence to therapy were associated with VF. At the time of VF, key PI-resistance mutations were detected in 11 (48%) of 23 patients who started on nelfinavir but were absent in 6 patients with indinavir treatment failure. PI plasma levels were more often below the range of active concentrations in VF with wild-type viruses (74%) than in VF with PI-resistant viruses (25%; P = .02). The mechanisms of early VF and of selection of PI-resistant viruses differed by type of PI and were dependent on PI plasma levels.
引用
收藏
页码:1503 / 1507
页数:5
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