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JAC Advance Access originally published online on August 13, 2003
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Journal of Antimicrobial Chemotherapy (2003) 52, 319-323
© 2003 The British Society for Antimicrobial Chemotherapy


Leading Article

Differentiation of genotypic resistance profiles for amprenavir and lopinavir, a valuable aid for choice of therapy in protease inhibitor-experienced HIV-1-infected subjects

Denise Paulsen1, Robert Elston2, Wendy Snowden2,*, Margaret Tisdale2 and Lisa Ross1,§

Department of International Clinical Virology, 1 GlaxoSmithKline Inc., 5 Moore Drive, Research Triangle Park, NC 27709, USA; 2 GlaxoSmithKline Research and Development, Stevenage, Hertfordshire SG1 2NY, UK

Keywords: amprenavir, lopinavir, genotype, resistance, HIV

The first 150 words of the full text of this article appear below.


    Introduction
 
One of the major challenges to the successful long-term treatment of HIV-1 infection is overcoming the development of increasing levels of antiretroviral resistance that often accompany the failure of successive treatment regimens. In order to meet this challenge a good understanding of genotypic resistance profiles and the potential for cross-resistance within each class of antiretrovirals is essential. For the protease inhibitors (PIs), cross-resistance is complex, as a result of the large number of mutations involved. Amprenavir and lopinavir are potent PIs used in ritonavir-boosted regimens, often in patients who have already experienced treatment with other PIs. The resistance profiles of these two PIs overlap to a certain extent but also contain some important differences that can be exploited in the choice of optimal treatment for PI-experienced patients. This article reviews our own research and that of others, in order to clarify the similarities and the differences between the genotypic resistance . . . [Full Text of this Article]


    In vitro and in vivo resistance profiles for amprenavir and lopinavir
 

    The impact of specific mutations on cross-resistance and response to amprenavir and lopinavir in PI-experienced subjects
 

    Cross-resistance between amprenavir and lopinavir
 

    Conclusions
 

    Acknowledgements
 

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