HIV protease genotype and viral sensitivity to HIV protease inhibitors following saquinavir therapy. NLM AIDSLINE Important note: Information in this article was accurate in 1999. The state of the art may have changed since the publication date.

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HIV protease genotype and viral sensitivity to HIV protease inhibitors following saquinavir therapy.

AIDS. 1998 Sep 10;12(13):1611-8. Unique Identifier : AIDSLINE MED/98435808
Craig C; Race E; Sheldon J; Whittaker L; Gilbert S; Moffatt A; Rose J; Dissanayeke S; Chirn GW; Duncan IB; Cammack N; Roche Discovery Welwyn, Welwyn Garden City, Herts, UK.


Abstract: OBJECTIVE: To examine the relationship between HIV protease genotype and altered protease inhibitor sensitivity of isolates from patients after therapy with saquinavir (SQV) in its hard gelatin formulation. DESIGN: Forty-one post-therapy isolates and corresponding baseline samples were obtained from 37 patients in four different clinical trials after therapy with SQV for 16-147 weeks. Post-therapy isolates were selected on the basis of preliminary sequence or drug sensitivity data. RESULTS: Fifteen out of 17 isolates without detectable Val-48 or Met-90 mutations retained sensitivity to SQV. (The remaining isolates showed only a marginal increase in median inhibitory concentration.) In addition, three out of 15 isolates with Met-90 retained sensitivity to all other protease inhibitors tested (indinavir, ritonavir, amprenavir, nelfinavir). Of the isolates showing reduced sensitivity to SQV, six out of 22 retained sensitivity to all other protease inhibitors, whereas only four out of 22 showed broad cross-resistance to all protease inhibitors tested. The reduction in sensitivity correlated closely with the presence of Val-48 or Met-90. Subsequent accessory substitutions were also linked to reduced sensitivity. However, significant linkage was observed only between mutations at residues 48 and 82 and between those at residues 82 and 74. CONCLUSIONS: Recruitment of Val-48/Met-90 mutations was not found to be synonymous with cross-resistance. Indeed, the majority of isolates with these mutations retained sensitivity to at least one protease inhibitor (Val-48, 86%; Met-90, 77%). The recruitment of accessory mutations may occur only after the selection of key resistance mutations. Furthermore, Met-90 was found to be a poor marker of cross-resistance in SQV-treated patients.
Keywords: JOURNAL ARTICLE Amino Acid Substitution Clinical Trials Databases, Factual DNA, Viral/CHEMISTRY Genotype Human HIV Infections/*DRUG THERAPY HIV Protease/DRUG EFFECTS/*GENETICS HIV Protease Inhibitors/*THERAPEUTIC USE Indinavir/THERAPEUTIC USE Linkage (Genetics) Methionine/ANALYSIS Nelfinavir/THERAPEUTIC USE Phenotype Polymerase Chain Reaction Ritonavir/THERAPEUTIC USE Saquinavir/*THERAPEUTIC USE Sulfonamides/THERAPEUTIC USE Valine/ANALYSISKWDjournalarticleaminoacidsubstitutionclinicaltrialsdatabases,factualdna,viral/chemistrygenotypehumanhivinfections/KWDdrugtherapyhivprotease/drugeffects/KWDgeneticshivproteaseinhibitors/KWDtherapeuticuseindinavir/therapeuticuselinkage(genetics)methionine/analysisnelfinavir/therapeuticusephenotypepolymerasechainreactionritonavir/therapeuticusesaquinavir/KWDtherapeuticusesulfonamides/therapeuticusevaline/analysis
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Copyright © 1999 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

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