Impact of 48 week lopinavir/ritonavir monotherapy on blood cell-associated HIV-1-DNA in the MONARK trial

被引:24
作者
Avettand-Fenoel, Veronique [1 ,2 ]
Flandre, Philippe [3 ,4 ]
Chaix, Marie-Laure [2 ]
Ghosn, Jade [2 ,5 ]
Delaugerre, Constance [2 ]
Raffi, Francois [6 ]
NgoVan, Philippe
Cohen-Codar, Isabelle
Delfraissy, Jean-Francois [5 ]
Rouzioux, Christine [2 ]
机构
[1] Hop Necker Enfants Malad, Virol Lab, CHU Necker Enfants Malad, AP HP, F-75015 Paris, France
[2] Univ Paris 05, EA3620, Paris, France
[3] INSERM, UMR S 943, Paris, France
[4] Univ Paris 06, Paris, France
[5] CHU Kremlin Bicetre, Le Kremlin Bicetre, France
[6] CHU Nantes, Nantes, France
关键词
HIV reservoirs; protease inhibitors; antiretroviral-naive patients; ACTIVE ANTIRETROVIRAL THERAPY; DNA; INFECTION; LOAD;
D O I
10.1093/jac/dkq084
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
To study the impact of protease inhibitor monotherapy on the HIV-1 blood reservoir in 72 antiretroviral-naive patients. This was evaluated for 72 antiretroviral-naive patients included in the on-treatment analysis of the MONARK trial; 46 patients receiving lopinavir/ritonavir monotherapy and 26 patients receiving a triple therapy. HIV-DNA was quantified in whole blood, using real-time PCR. The decrease in HIV-DNA after 48 weeks of lopinavir/ritonavir monotherapy was similar to the decrease observed with triple therapy including lopinavir/ritonavir (-0.77 versus -0.69 log copies/10(6) leucocytes, respectively; P = 0.91). The HIV-DNA decrease was also similar in patients with a virological response in both arms (-0.69 versus -0.69 log copies/10(6) leucocytes, respectively). Interestingly, non-responders had a significantly higher baseline HIV-DNA load than responders in the monotherapy arm; 3.16 versus 2.86 log copies/10(6) leucocytes, respectively (P = 0.05). The MONARK data indicate that a lopinavir/ritonavir monotherapy regimen is potent against HIV blood reservoirs in antiretroviral-naive patients after 1 year of treatment, in comparison with a standard-of-care highly active antiretroviral therapy. This impact should be evaluated with other boosted protease inhibitor monotherapies.
引用
收藏
页码:1005 / 1007
页数:3
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