Persistence of mutidrug-resistant HIV-1 in primary infection leading to superinfection

被引:96
作者
Brenner, B
Routy, J
Quan, YD
Moisi, D
Oliveira, M
Turner, D
Wainberg, MA
Baril, JG
Bélanger, M
Côté, P
Dufresne, S
Leplante, F
Lebel, J
Boissonnault, M
Lavoie, H
Lessard, B
Olivier, C
Trottier, RB
Vézina, S
Gilmore, N
Klein, M
Lalonde, P
MacLeod, J
Smith, G
Cholette, P
Laponte, N
Samson, J
Frenette, C
Valois, C
Bélanger, M
机构
[1] McGill Univ, Jewish Gen Hosp, McGill AIDS Ctr, Montreal, PQ H3T 1E2, Canada
[2] McGill Univ, Ctr Hlth, Montreal, PQ, Canada
关键词
HIV transmission; viral load; drug resistance; M184v mutation;
D O I
10.1097/01.aids.0000131377.28694.04
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: The authors previous studies documented persistence of multidrug resistance (MDR) acquired in five primary HIV-1 infection (PHI) cases for 1-2 years in the absence of antiretroviral treatment. This study characterizes the evolution of transmitted wild-type (WT) (n = 15), resistant (n = 10), and MDR (n = 6) infections. Longterm persistence of MDR infections (2-7 years), leading to one observed MDR superinfection is documented. Methods: Genotypic changes in circulating viral quasi-species were evaluated over 1.5-7 years in patients (n = 31) enrolled in the PHI study. Sequencing of reverse transcriptase and protease regions identified nucleotide substitutions in the viral quasi-species and mutations at sites implicated in resistance to antiretroviral drugs. Phylogenetic and clonal analysis were performed to confirm one observed superinfection. Results: Patients acquiring WT, drug-resistant and MDR infections showed little quasi-species evolution (> 99.6% homology) for more than 1.5 years, regardless of route of transmission. Transmitted resistance mutations (other than 184 V) persisted for 2-7 years. MDR persistence in two PHI cases contrasted with the corresponding rapid reversion of MDR infections to WT in their partners following treatment interruption. One MDR transmission eliciting low-level viremia resulted in clearance of the original MDR infection followed by re-infection with a second heterologous MDR strain from a different partner. Phylogenetic and clonal analysis of source and index partner confirmed the superinfection. Both MDR species showed approximately 13-fold reductions in replication capacity relative to the homologous WT strain isolated from the source partner. Conclusions: Genotypic analysis in PHI may identify superinfection and MDR infections that represent important determinants of virological and treatment outcome. (C) 2004 Lippincott Williams Wilkins.
引用
收藏
页码:1653 / 1660
页数:8
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