Overcoming resistance to existing therapies in HIV‐infected patients: The role of new antiretroviral drugs
- 22 February 2008
- journal article
- review article
- Published by Wiley in Journal of Medical Virology
- Vol. 80 (4) , 565-576
- https://doi.org/10.1002/jmv.21034
Abstract
Resistance to available antiretroviral (ARV) agents is of increasing concern, and development of novel agents that address this problem has been identified as a major public health priority. As ARV resistance becomes more prevalent with extended use of existing agents, individuals with HIV infection resistant to all three traditional classes of ARVs, nucleoside reverse transcriptase inhibitors (NRTIs), non‐nucleoside reverse transcriptase inhibitors (NNRTIs) and protease inhibitors (PIs), find themselves increasingly limited with regard to effective treatment options. The need for tolerable new drug regimens that effectively suppress viral replication while being simple to adhere to is increasingly pressing. This article reviews the epidemiology of antiretroviral drug resistance, the factors that contribute to the emergence of resistance, and presents data that support the need for early detection of resistance and maximal virologic suppression in order to delay treatment failure and reduce mortality. Healthcare providers are encouraged to optimize therapy through the use of new agents from existing drug classes, which can minimize cross‐resistance, as well as agents with novel mechanisms of action, in order to realize the potential for greater viral containment and to forestall development of resistance mutations. This article evaluates several emerging therapies that are in late‐stage clinical development and promise to expand treatment options for highly treatment‐experienced patients with the goal of improving outcomes for HIV‐infected individuals whose options for sustained antiviral efficacy are increasingly limited. J. Med. Virol. 80:565–576, 2008.Keywords
This publication has 51 references indexed in Scilit:
- Relative antiviral efficacy of ritonavir-boosted darunavir and ritonavir-boosted tipranavir vs. control protease inhibitor in the POWER and RESIST trialsHIV Medicine, 2007
- Interruption of combination antiretroviral therapy and risk of clinical disease progression to AIDS or deathHIV Medicine, 2007
- High Prevalence of the K65R Mutation in Human Immunodeficiency Virus Type 1 Subtype C Isolates from Infected Patients in Botswana Treated with Didanosine-Based RegimensAntimicrobial Agents and Chemotherapy, 2006
- Specific mutations in HIV-1 gp41 are associated with immunological success in HIV-1-infected patients receiving enfuvirtide treatmentJournal of Antimicrobial Chemotherapy, 2006
- Concomitant Use of an Active Boosted Protease Inhibitor with Enfuvirtide in Treatment-Experienced, HIV-Infected Individuals: Recent Data and Consensus RecommendationsHIV Research & Clinical Practice, 2006
- Prevalence of resistance-associated mutations in newly diagnosed HIV-1 patients in GreeceVirus Research, 2005
- Safety, Pharmacokinetics, and Efficacy of (+/−)-β-2′,3′-Dideoxy-5-Fluoro-3′-Thiacytidine with Efavirenz and Stavudine in Antiretroviral-Naïve Human Immunodeficiency Virus-Infected PatientsAntimicrobial Agents and Chemotherapy, 2005
- Relationship between drug resistance mutations, plasma viremia, and CD4+T-cell counts in patients with chronic HIV infectionJournal of Medical Virology, 2005
- How Does Expert Advice Impact Genotypic Resistance Testing in Clinical Practice?Clinical Infectious Diseases, 2003
- HIV-1 Dynamics in Vivo: Virion Clearance Rate, Infected Cell Life-Span, and Viral Generation TimeScience, 1996