Influence of MDR1 C1236T polymorphism on lopinavir plasma concentration and virological response in HIV-1-infected children.

Abstract Background Variability in MDR1 and PXR has been associated with differences in drug plasma levels and response to antiretroviral therapy. We investigated whether polymorphisms in MDR1 (T-129C, C1236T and C3435T) and PXR (C63396T) affect lopinavir plasma concentration and the virological or immunological response to HAART in HIV-1-infected children. Methods Genotypes were identified in 100 blood donors and 38 HIV-1-infected children. All children received HAART with lopinavir boosted with ritonavir (LPV/r) at the time of LPV plasma level quantification, before (C trough ) and between 1 and 2 h after (C post-dose ) the administration of the next dose of drug. CD4 + T-cell counts and plasma viral load were analyzed before and after the initiation of LPV/r. Results MDR1 1236T, MDR1 3435T and PXR 63396T alleles showed a frequency of ~ 50% while the MDR1 -129C allele only reached 5%. Children heterozygotes 1236CT showed a significantly lower LPV C post-dose than homozygotes 1236TT (median C post-dose  = 3.04 μg/ml and 6.50 μg/ml, respectively; p  = 0.016). Children heterozygotes 1236CT also had a lower decrease of viral load after 36 weeks of LPV/r exposure compared with homozygotes 1236CC (median viral load changes = − 0.50 log 10 copies/ml and − 2.08 log 10 copies/ml, respectively; p  = 0.047). No effect on the immunological response was observed for polymorphisms of MDR1 or PXR. Conclusions Our results suggest that the MDR1 C1236T SNP significantly reduces LPV plasma concentration affecting the virological response to HAART. Heterozygotes 1236CT might have an altered level of P-gp expression/activity in enterocytes and CD4 + T lymphocytes that limits the absorption of LPV leading to an impaired virological suppression.