Maturation Inhibitors: a New Therapeutic Class Targets the Virus Structure

Maturation Inhibitors: a New Therapeutic Class Targets the Virus Structure

Karl Salzwedel 1, David E. Martin 1, Michael Sakalian 1

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*Correspondence: David E. Martin, Email not available

Abstract

The current standard of care for HIV/AIDS in the developed world is HAART therapy, usually a combinationof two reverse transcriptase inhibitors and a protease inhibitor. Despite the success of this regimen,there is a continuing need for new drug options to overcome problems with tolerability and the emergenceof viral resistance. In this review we discuss the discovery of a potential new class of antiretroviraltherapeutics, known as maturation inhibitors, and the development of the first-in-class compound, bevirimat.Bevirimat is distinguished from the currently available antiretrovirals by its unique target andmode of action. While the specific interactions responsible for activity have yet to be fully characterized,it is clear that the target for bevirimat is the Gag polyprotein precursor, the main structural protein responsiblefor assembly and budding of virion particles. As basic research continues on the precisemechanism of action of bevirimat, clinical development is progressing, with demonstration of bothsafety and efficacy in early-stage trials. These encouraging results, coupled with the discovery and developmentof future generations of maturation inhibitors, suggest that maturation inhibitors may beadded to the growing set of tools available to control HIV/AIDS.

Keywords: HIV. Inhibitor. Virus assembly. Gag protein. Drug development.

Contents

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