Pharmacovirological analyses of blood and male genital compartment in patients receiving dolutegravir plus lamivudine dual therapy as a switch strategy (ANRS 167 LAMIDOL trial)

被引:13
作者
Charpentier, Charlotte [1 ,2 ]
Peytavin, Gilles [1 ,3 ]
Raffi, Francois [4 ,5 ]
Burdet, Charles [1 ,6 ]
Landman, Roland [1 ,7 ]
Le, Minh P. [1 ,3 ]
Katlama, Christine [8 ]
Collin, Gilles [1 ,2 ]
Benalycherif, Aida [9 ]
Cabie, Andre [10 ,11 ]
Mentre, France [1 ,6 ]
Yazdanpanah, Yazdan [1 ,7 ]
Descamps, Diane [1 ,2 ]
Joly, Veronique [1 ,7 ]
机构
[1] Univ Paris, INSERM, UMR 1137, IAME, F-75018 Paris, France
[2] Hop Bichat Claude Bernard, AP HP, Lab Virol, F-75018 Paris, France
[3] Hop Bichat Claude Bernard, Lab Pharmacol Toxicol, F-75018 Paris, France
[4] CHU Hotel Dieu, Infect Dis Dept, Nantes, France
[5] Nantes Univ, INSERM UIC 1413, Nantes, France
[6] Hop Bichat Claude Bernard, Dept Epidemiol Biostat & Rech Clin, F-75018 Paris, France
[7] Hop Bichat Claude Bernard, Serv Malad Infect & Trop, F-75018 Paris, France
[8] Hop La Pitie Salpetriere, AP HP, Serv Malad Infect & Trop, Paris, France
[9] Fdn Leon Mba, IMEA, Paris, France
[10] Univ Antilles, Fort De France, Martinique, France
[11] CHU Martinique, Serv Malad Infect & Trop, Fort De France, Martinique, France
关键词
UNDETECTABLE HIV-1 RNA; SEMINAL PLASMA SAMPLES; ANTIRETROVIRAL DRUGS; TREATED PATIENTS; SEMEN; ADULTS; MEN; SEX; RILPIVIRINE; INFECTION;
D O I
10.1093/jac/dkaa035
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To describe plasma residual HIV viraemia, cellular HIV reservoir size, blood plasma drug concentrations and their male genital tract penetration during the maintenance dual therapy dolutegravir+lamivudine. Patients and methods: ANRS167 LAMIDOL enrolled 104 virologically suppressed patients to switch to dolutegravir+lamivudine. In this pharmacovirological substudy, ultrasensitive plasma viral load (USpVL) and plasma drug concentrations were measured at Day 0 (D0), Week 24 (W24) and W48 of dolutegravir+lamivudine, and HIV-DNA was measured at W-8 and W48. Semen samples were collected at D0 and W24 from 18 participants. Total and unbound blood and seminal plasma drug concentrations were measured using UPLC-MS/MS. Results: Median HIV-DNA was 2.5log(10)copies/10(6) PBMC (IQR=2.2-3.0, n=100) at W-8 and 2.4log(10)copies/10(6) PBMC (IQR=2.1-2.9, n=100) at W48 (P=0.17). The proportion of patients with undetected USpVL was 38% (n=98), 43% (n=98) and 49% (n=97) at D0, W24 and W48, respectively (P=0.08). Total and unbound plasma dolutegravir concentrations were stable between timepoints (P=0.13) and all total plasma dolutegravir concentrations except one were adequate. Median free fraction of dolutegravir in plasma was 0.21%. Median blood plasma and seminal plasma concentrations of total dolutegravir at 24h were 1812ng/mL and 206ng/mL, respectively. Median seminal plasma/blood plasma total concentration ratios were 11.6% and 2478% for dolutegravir and lamivudine, respectively. HIV-RNA (365 to 475copies/mL) was detected in seminal plasma of one patient at D0 (5.9%) and of two patients at W24 (11.8%). Conclusions: These findings add further important information regarding the effectiveness of dolutegravir+lamivudine maintenance dual therapy in terms of plasma residual viraemia, cellular reservoir size and drug penetration in the male genital tract.
引用
收藏
页码:1611 / 1617
页数:7
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