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Updated: Jul 5, 2026

07:06
Prediction of HIV-1 Coreceptor Usage (Tropism) by Sequence Analysis using a Genotypic Approach
Published on: December 1, 2011
[Maraviroc: clinical trials results]
1Service de Maladies Infectieuses et Tropicales, Hôpital de la Croix Rousse, Lyon cedex 04, France. christian.chidiac@chu-lyon.fr
Medecine Et Maladies Infectieuses
|December 17, 2008
Summary
Maraviroc, a new CCR5 antagonist, is approved for HIV treatment in adults with CCR5-tropic virus. This entry inhibitor blocks viral entry into cells, showing efficacy and a similar safety profile to placebo in trials.
Area of Science:
- Virology
- Immunology
- Pharmacology
Background:
- Chemokine receptors CCR5 and CXCR4 are coreceptors for HIV.
- Maraviroc is the first CCR5 antagonist approved for HIV treatment.
- Entry inhibitors, like maraviroc, block viral cell entry, unlike traditional antiretrovirals.
Purpose of the Study:
- To review the efficacy and safety of maraviroc, a CCR5 antagonist.
- To discuss the role of viral tropism testing in maraviroc therapy.
- To explore the potential future applications of maraviroc in HIV treatment.
Main Methods:
- Clinical efficacy and safety data from large phase III trials were assessed.
- The mechanism of action of CCR5 antagonists was reviewed.
- Viral tropism testing requirements for maraviroc use were highlighted.
Main Results:
- Maraviroc demonstrated clinical efficacy in patients with treatment-experienced HIV.
- Its safety profile in trials was comparable to placebo.
- CCR5 antagonists are ineffective against CXCR4-tropic HIV, necessitating tropism testing.
Conclusions:
- Maraviroc represents a novel therapeutic option for specific HIV-1 infections.
- Further assessment of hepatic and immunologic safety is warranted for CCR5 antagonists.
- Future research may expand maraviroc's use beyond treatment-experienced patients.
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