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BMC Med. 2012; 10: 34.
Published online Apr 12, 2012. doi:  10.1186/1741-7015-10-34
PMCID: PMC3348091
Novel therapeutic strategies targeting HIV integrase
Peter K Quashie,1,2 Richard D Sloan,1 and Mark A Wainbergcorresponding author1,2,3
1McGill University AIDS Centre, Lady Davis Institute, Montreal, Canada
2Division of Experimental Medicine, McGill University, Montreal, Canada
3Department of Microbiology and Immunology, McGill University, Montreal, Canada
corresponding authorCorresponding author.
Peter K Quashie: peter.quashie/at/mail.mcgill.ca; Richard D Sloan: Richard.sloan/at/mail.mcgill.ca; Mark A Wainberg: mark.wainberg/at/mcgill.ca
Received December 5, 2011; Accepted April 12, 2012.
Abstract
Integration of the viral genome into host cell chromatin is a pivotal and unique step in the replication cycle of retroviruses, including HIV. Inhibiting HIV replication by specifically blocking the viral integrase enzyme that mediates this step is an obvious and attractive therapeutic strategy. After concerted efforts, the first viable integrase inhibitors were developed in the early 2000s, ultimately leading to the clinical licensure of the first integrase strand transfer inhibitor, raltegravir. Similarly structured compounds and derivative second generation integrase strand transfer inhibitors, such as elvitegravir and dolutegravir, are now in various stages of clinical development. Furthermore, other mechanisms aimed at the inhibition of viral integration are being explored in numerous preclinical studies, which include inhibition of 3' processing and chromatin targeting. The development of new clinically useful compounds will be aided by the characterization of the retroviral intasome crystal structure. This review considers the history of the clinical development of HIV integrase inhibitors, the development of antiviral drug resistance and the need for new antiviral compounds.
Keywords: crystal structure, dolutegravir, HIV integrase, mutations, new drugs, raltegravir, resistance
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