JAC Advance Access originally published online on August 13, 2003
Journal of Antimicrobial Chemotherapy (2003) 52, 319-323
© 2003 The British Society for Antimicrobial Chemotherapy
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
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Introduction
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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
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In vitro and in vivo resistance profiles for amprenavir and lopinavir
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The impact of specific mutations on cross-resistance and response to amprenavir and lopinavir in PI-experienced subjects
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Cross-resistance between amprenavir and lopinavir
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Conclusions
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Acknowledgements
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