Lopinavir/ritonavir: a protease inhibitor for HIV-1 treatment

被引:19
|
作者
Barragan, Patricia [1 ]
Podzamczer, Daniel [1 ]
机构
[1] Hosp Univ Bellvitge, Barcelona 08907, Spain
关键词
HIV-1; treatment; lopinavir/ritonavir; protease inhibitor;
D O I
10.1517/14656566.9.13.2363
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Lopinavir is a protease inhibitor with high specificity for HIV-1 protease formulated with ritonavir. Numerous clinical trials have shown that lopinavir/ritonavir (LPV/r) is highly effective as a component of highly active antiretroviral therapy (HAART) regimens for HIV-1 infection. Objective: In this article we provide an overview of the properties of LPV/r and the experience with its use in HIV-infected adults and adolescents. Methods: We reviewed the literature and selected the most important published articles on LPV/r and the latest posters/communications presented in conferences, with particular attention to the clinical efficacy and tolerability of LPV/r in HIV-1 infected patients. Conclusion: LPV/r is highly effective as a component of HAART regimens for HIV-1 infection. There is considerable experience with the drug in both treatment-naive and treatment-experienced patients. In general, LPV/r is well tolerated and its high genetic barrier to resistance favours long-term efficacy.
引用
收藏
页码:2363 / 2375
页数:13
相关论文
共 50 条
  • [21] Lopinavir/Ritonavir A Review of its Use in the Management of HIV-1 Infection
    Croxtall, Jamie D.
    Perry, Caroline M.
    DRUGS, 2010, 70 (14) : 1885 - 1915
  • [22] The protease inhibitor lopinavir, boosted with ritonavir, as treatment for COVID-19: a rapid review
    Dorward, Jienchi
    Gbinigie, Oghenekome
    Cai, Ting
    Roberts, Nia W.
    Garrett, Nigel
    Hayward, Gail
    Butler, Christopher C.
    ANTIVIRAL THERAPY, 2020, 25 (07) : 365 - 376
  • [23] Characterization of extracellular vesicles (exosomes) from HIV-1 infected macrophages treated with HIV-1 protease inhibitor, Ritonavir.
    Deshmane, Satish
    Sheffield, Joel
    Khalili, Kamel
    Datta, Prasun
    JOURNAL OF NEUROVIROLOGY, 2015, 21 : S17 - S17
  • [25] Amprenavir - A protease inhibitor for the treatment of patients with HIV-1 infection
    Reddy, P
    Ross, J
    FORMULARY, 1999, 34 (07) : 567 - +
  • [26] A folding inhibitor of the HIV-1 protease
    Broglia, RA
    Provasi, D
    Vasile, F
    Ottolina, G
    Longhi, R
    Tiana, G
    PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2006, 62 (04) : 928 - 933
  • [27] Cerebrospinal fluid and plasma HIV-1 RNA levels and lopinavir concentrations following lopinavir/ritonavir regimen
    Yilmaz, A
    Ståhle, L
    Hagberg, L
    Svennerholm, B
    Fuchs, D
    Gisslén, M
    SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 2004, 36 (11-12) : 823 - 828
  • [28] A SHORT-TERM STUDY OF THE SAFETY, PHARMACOKINETICS, AND EFFICACY OF RITONAVIR, AN INHIBITOR OF HIV-1 PROTEASE
    DANNER, SA
    CARR, A
    LEONARD, JM
    LEHMAN, LM
    GUDIOL, F
    GONZALES, J
    RAVENTOS, A
    RUBIO, R
    BOUZA, E
    PINTADO, V
    AGUADO, AG
    DELOMAS, JG
    DELGADO, R
    BORLEFFS, JCC
    HSU, A
    VALDES, JM
    BOUCHER, CAB
    COOPER, DA
    GIMENO, C
    CLOTET, B
    TOR, J
    FERRER, E
    MARTINEZ, PL
    MORENO, S
    ZANCADA, G
    ALCAMI, J
    NORIEGA, AR
    PULIDO, F
    GLASSMAN, HN
    NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (23): : 1528 - 1533
  • [29] The HIV protease inhibitor lopinavir/ritonavir (Kaletra) alters the growth, differentiation and proliferation of primary gingival epithelium
    Israr, M.
    Mitchell, D.
    Alam, S.
    Dinello, D.
    Kishel, J. J.
    Meyers, C.
    HIV MEDICINE, 2011, 12 (03) : 145 - 156
  • [30] Farnesyltransferase inhibitors prevent HIV protease inhibitor (lopinavir/ritonavir)-induced lipodystrophy and metabolic syndrome in mice
    Tanaka, Tomokazu
    Nakazawa, Harumasa
    Kuriyama, Naohide
    Kaneki, Masao
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2018, 15 (02) : 1314 - 1320