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HIV-1 integrase inhibitor resistance and its clinical implications.

ABSTRACT: With the approval in 2007 of the first integrase inhibitor (INI), raltegravir, clinicians became better able to suppress virus replication in patients infected with human immunodeficiency virus type 1 (HIV-1) who were harboring many of the most highly drug-resistant viruses. Raltegravir also provided clinicians with additional options for first-line therapy and for the simplification of regimens in patients with stable virological suppression. Two additional INIs in advanced clinical development-elvitegravir and S/GSK1349572-may prove equally versatile. However, the INIs have a relatively low genetic barrier to resistance in that 1 or 2 mutations are capable of causing marked reductions in susceptibility to raltegravir and elvitegravir, the most well-studied INIs. This perspective reviews the genetic mechanisms of INI resistance and their implications for initial INI therapy, the treatment of antiretroviral-experienced patients, and regimen simplification.

SUBMITTER: Blanco JL

PROVIDER: S-EPMC3069732 | biostudies-literature | 2011 May

REPOSITORIES: biostudies-literature

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HIV-1 integrase inhibitor resistance and its clinical implications.

Blanco Jose-Luis JL Varghese Vici V Rhee Soo-Yon SY Gatell Jose M JM Shafer Robert W RW

The Journal of infectious diseases 20110501 9

With the approval in 2007 of the first integrase inhibitor (INI), raltegravir, clinicians became better able to suppress virus replication in patients infected with human immunodeficiency virus type 1 (HIV-1) who were harboring many of the most highly drug-resistant viruses. Raltegravir also provided clinicians with additional options for first-line therapy and for the simplification of regimens in patients with stable virological suppression. Two additional INIs in advanced clinical development ...[more]

PMID: 21459813

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