Literature DB >> 17933723

CCR5 antagonists in the treatment of treatment-experienced patients infected with CCR5 tropic HIV-1.

Thore Lorenzen1, Albrecht Stoehr, Irene Walther, Andreas Plettenberg.   

Abstract

CCR5 antagonists are a newly developed class of antiretroviral drugs which inhibit viral entry into the host cell by binding to the predominant HIV coreceptor. Data on the use of these new drugs in treatment-experienced HIV patients are emerging. Clinical trials on maraviroc and vicriviroc in pretreated patients recruited more than 1300 individuals. Interim results of these studies indicate that pretreated patients infected with CCR5-tropic viruses benefit from their use in optimized combination regimens. Maraviroc reduces the HIV-1 viral load in patients with previous triple-class failure by 1.96 log10 copies/ml versus 0.99 log10 copies/ml in placebo; vicriviroc shows potency by dose depending viral decrease of 1.51-1.68 log10 copies/ml compared to 0.29 log10 in placebo. As expected, CCR5 antagonists do not reduce viral load in patients harbouring CXCR4-tropic or dual/mixed tropic viruses. Nevertheless, since a considerable percentage of late-stage HIV patients still bear CCR5-tropic viruses, the use of CCR5 antagonists appears promising in properly selected treatment-experienced patients.

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Year:  2007        PMID: 17933723

Source DB:  PubMed          Journal:  Eur J Med Res        ISSN: 0949-2321            Impact factor:   2.175


  3 in total

Review 1.  Pharmacologic aspects of new antiretroviral drugs.

Authors:  Mary C Long; Jennifer R King; Edward P Acosta
Journal:  Curr HIV/AIDS Rep       Date:  2009-02       Impact factor: 5.495

2.  Pharmacologic aspects of new antiretroviral drugs.

Authors:  Mary C Long; Jennifer R King; Edward P Acosta
Journal:  Curr Infect Dis Rep       Date:  2008-11       Impact factor: 3.663

Review 3.  Pharmacogenetic testing and therapeutic drug monitoring are complementary tools for optimal individualization of drug therapy.

Authors:  Guillermo Gervasini; Julio Benítez; Juan Antonio Carrillo
Journal:  Eur J Clin Pharmacol       Date:  2010-06-27       Impact factor: 3.064

  3 in total

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