Abstract
The success of first-line antiretroviral therapy can be challenged by the acquisition of primary drug resistance. Here we report a case where baseline genotypic resistance testing detected resistance conferring nucleoside/ nucleotide reverse transcriptase inhibitor (NRTI)-associated mutations, but no primary mutations for protease inhibitor (PI). Subsequent PI-based HAART with boosted saquinavir led to virological treatment success with persistently undetectable viral load. After treatment simplification from saquinavir to an atazanavir based PI-therapy and no change in backbone therapy rapid virological breakthrough occurred. Retrospective analysis displayed preexisting gag cleavage site mutations which may have reduced the genetic barrier in a clinical relevant manner in combination with the already existing NRTI resistance mutations. Alternatively, this effect could be explained with a different antiviral potency for the respective PIs used. © I. Holzapfel Publishers 2010.
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Anadol, E., Kaiser, R., Verheyen, J., Schülter, E., Emmelkamp, J., Schwarze-Zander, C., … Rockstroh, J. K. (2010). Transmission of human immunodeficiency virus I drug resistance - A case report. What are the clinical implications? European Journal of Medical Research, 15(5), 225–230. https://doi.org/10.1186/2047-783x-15-5-225
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