Preventing and managing antiretroviral drug resistance
- PMID: 15186710
- DOI: 10.1089/108729104323076007
Preventing and managing antiretroviral drug resistance
Abstract
Development of resistance to antiretroviral drugs (ARVs) is a major impediment to optimum treatment of HIV-1 infection. Although resistance testing can help to select subsequent regimens when virologic failure occurs, cross-resistance, which affects all classes of ARVs, may make it more difficult to achieve optimum control of HIV. We have known for some time that our first choice of antiretroviral therapy offers the best chance to control HIV replication and that initial therapy should be selected with an eye on future options. Potency is the first line of defense against the development of resistance. Other factors that affect resistance development include: tolerability, potential for optimum adherence, and genetic and pharmacologic barriers to development of resistance. If resistance emerges, only a single drug may be affected initially, and a rapid change in ARVs may preserve the efficacy of other components. One cautionary note is that we can no longer assume that a patient's HIV is fully susceptible to all ARVs even in the initial regimen. Transmission of drug-resistant HIV means that the genetic composition may be that of an "experienced" virus with reduced susceptibility to ARVs. Resistance testing at the time of transmission is most likely to reveal this resistance, but over time the dominant genetic pattern may revert to wild-type, and be missed by resistance testing. Because "archived" resistant HIV may emerge quickly once treatment is initiated, we need to keep this in mind when selecting initial therapy.
Similar articles
-
Study of the impact of HIV genotypic drug resistance testing on therapy efficacy.Verh K Acad Geneeskd Belg. 2001;63(5):447-73. Verh K Acad Geneeskd Belg. 2001. PMID: 11813503 Review.
-
High level of HIV-1 resistance in patients failing long-term first-line antiretroviral therapy in Mali.J Antimicrob Chemother. 2014 Sep;69(9):2531-5. doi: 10.1093/jac/dku153. Epub 2014 May 22. J Antimicrob Chemother. 2014. PMID: 24855120
-
Assessing resistance costs of antiretroviral therapies via measures of future drug options.J Infect Dis. 2003 Oct 1;188(7):1001-8. doi: 10.1086/378355. Epub 2003 Sep 23. J Infect Dis. 2003. PMID: 14513420
-
Persistence of HIV-1 drug resistance mutations and emergence during antiretroviral treatment interruption: considerations from a clinical case.Med Sci Monit. 2003 Apr;9(4):CS16-9. Med Sci Monit. 2003. PMID: 12709675
-
Antiretroviral therapy for HIV: drug resistance and sequencing.J Assoc Nurses AIDS Care. 2002 Jan-Feb;13(1):76-80. doi: 10.1016/S1055-3290(06)60243-4. J Assoc Nurses AIDS Care. 2002. PMID: 11828862 Review. No abstract available.
Cited by
-
Development and Characterization of Printlets of Lamivudine for Pediatric Patients Using Selective Laser Sintering.Pharmaceuticals (Basel). 2025 Mar 1;18(3):356. doi: 10.3390/ph18030356. Pharmaceuticals (Basel). 2025. PMID: 40143133 Free PMC article.
-
Polymorphisms and drug resistance analysis of HIV-1 isolates from patients on first line antiretroviral therapy (ART) in South-eastern Nigeria.PLoS One. 2020 Apr 8;15(4):e0231031. doi: 10.1371/journal.pone.0231031. eCollection 2020. PLoS One. 2020. PMID: 32267869 Free PMC article.
-
Medication Adherence and HIV Symptom Distress in Relation to Panic Disorder Among HIV-Positive Adults Managing Opioid Dependence.Cognit Ther Res. 2014 Aug;38(4):458-464. doi: 10.1007/s10608-014-9608-x. Cognit Ther Res. 2014. PMID: 26146476 Free PMC article.
-
Laboratory monitoring to guide switching antiretroviral therapy in resource-limited settings: clinical benefits and cost-effectiveness.J Acquir Immune Defic Syndr. 2010 Jul;54(3):258-68. doi: 10.1097/QAI.0b013e3181d0db97. J Acquir Immune Defic Syndr. 2010. PMID: 20404739 Free PMC article.
-
Treatment exhaustion of highly active antiretroviral therapy (HAART) among individuals infected with HIV in the United Kingdom: multicentre cohort study.BMJ. 2005 Mar 26;330(7493):695. doi: 10.1136/bmj.38369.669850.8F. Epub 2005 Mar 4. BMJ. 2005. PMID: 15749728 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical