Publication | Open Access
Q151M‐Mediated Multinucleoside Resistance: Prevalence, Risk Factors, and Response to Salvage Therapy
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2004
Year
ImmunologyPharmacotherapyLamivudine AdministrationImmunotherapySalvage TherapyDrug ResistanceHuman RetrovirusResistance Mutation (Virology)Multinucleoside ResistanceHealth SciencesPrimary ImmunodeficiencyAutoimmune DiseaseChronic Viral InfectionHivPharmacologyRisk FactorsInborn Error Of ImmunityTreatment InterruptionQ151m MutationMedicineTherapy Resistance
Among 470 patients with acquired immune deficiency syndrome and/or human immunodeficiency virus infection (HIV/AIDS) who underwent genotype resistance testing (GRT) after the failure of therapy, 17 (3.6%) harbored the Q151M mutation. The Q151M mutation was associated with younger age, lower CD4(+) lymphocyte count, higher HIV RNA level, and treatment with >2 pre-GRT regimens. By contrast, the Q151M mutation was inversely associated with lamivudine administration. A full reversion of the Q151M mutation was observed in 5 of 5 patients who underwent treatment interruption after GRT. The reversion was followed by a response to salvage therapy in 4 (80%) of 5 patients.
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