HIV-1 drug resistance mutations emerging on darunavir therapy in PI-naive and -experienced patients in the UK

被引:21
作者
El Bouzidi, Kate [1 ,2 ]
White, Ellen [3 ]
Mbisa, Jean L. [4 ]
Sabin, Caroline A. [1 ]
Phillips, Andrew N. [1 ]
Mackie, Nicola [5 ]
Pozniak, Anton L. [6 ]
Tostevin, Anna [3 ]
Pillay, Deenan [2 ,7 ]
Dunn, David T. [3 ]
机构
[1] UCL, Res Dept Infect & Populat Hlth, London, England
[2] UCL, Res Dept Infect, Div Infect & Immun, London, England
[3] MRC Clin Trials Unit UCL, London, England
[4] Publ Hlth England, Virus Reference Dept, Ctr Infect, London, England
[5] Imperial Coll Healthcare NHS Trust, Dept HIV Med, London, England
[6] Chelsea & Westminster Hosp NHS Fdn Trust, Dept Med, London, England
[7] Univ KwaZulu Natal, Wellcome Trust Africa Ctr Hlth & Populat Sci, Mtubatuba, South Africa
基金
英国医学研究理事会; 英国惠康基金;
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; PROTEASE INHIBITOR; INFECTED PATIENTS; SUBTYPE B; GAG; SUSCEPTIBILITY; SELECTION; DARUNAVIR/RITONAVIR; LOPINAVIR/RITONAVIR; SEQUENCES;
D O I
10.1093/jac/dkw343
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Darunavir is considered to have a high genetic barrier to resistance. Most darunavir-associated drug resistance mutations (DRMs) have been identified through correlation of baseline genotype with virological response in clinical trials. However, there is little information on DRMs that are directly selected by darunavir in clinical settings. Objectives: We examined darunavir DRMs emerging in clinical practice in the UK. Patients and methods: Baseline and post-exposure protease genotypes were compared for individuals in the UK Collaborative HIV Cohort Study who had received darunavir; analyses were stratified for PI history. A selection analysis was used to compare the evolution of subtype B proteases in darunavir recipients and matched PI-naive controls. Results: Of 6918 people who had received darunavir, 386 had resistance tests pre- and post-exposure. Overall, 2.8% (11/386) of these participants developed emergent darunavir DRMs. The prevalence of baseline DRMs was 1.0% (2/198) among PI-naive participants and 13.8% (26/188) among PI-experienced participants. Emergent DRMs developed in 2.0% of the PI-naive group (4 mutations) and 3.7% of the PI-experienced group (12 mutations). Codon 77 was positively selected in the PI-naive darunavir cases, but not in the control group. Conclusions: Our findings suggest that although emergent darunavir resistance is rare, it may be more common among PI-experienced patients than those who are PI-naive. Further investigation is required to explore whether codon 77 is a novel site involved in darunavir susceptibility.
引用
收藏
页码:3487 / 3494
页数:8
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