Rapid development of antiretroviral drug resistance mutations in HIV-infected children less than two years of age initiating protease inhibitor-based therapy in South Africa

AIDS Res Hum Retroviruses. 2011 Sep;27(9):945-56. doi: 10.1089/aid.2010.0205. Epub 2011 Mar 23.

Abstract

Data on the development of antiretroviral drug resistance in HIV-1-infected children receiving protease inhibitor (PI)-based antiretroviral therapy (ART) are limited. We examined antiretroviral resistance among a cohort of 323 South African HIV-infected children <2 years old exposed to nevirapine for prevention of mother-to-child transmission. Ritonavir (RTV) was used initially for 138 children who were <6 months old or receiving antimycobacterial therapy; otherwise children received lopinavir/ritonavir (LPV/r)-based ART. HIV-1 population sequencing of the pol gene was conducted on all pretreatment samples and on posttreatment samples for children who did not achieve HIV-1 plasma RNA <400 copies/ml by 52 weeks. Among children in the cohort, 38 died, 22 had <24 weeks follow-up, 209 achieved virologic suppression, and 54 did not. Of 41 children without virologic suppression with posttreatment HIV genotype data available, major resistance mutations were found in 32 (78%): 14 (36%) had PI mutations including V82A, M46I, and L90M; 29 (71%) had M184V/I; and three had NNRTI mutations (K103N, Y181C, and G190A). Among the children who did not achieve virologic suppression, none of the seven children treated exclusively with LPV/r developed PI-related mutations, compared with 14 of 32 (44%) who received RTV-based regimens (p=0.036); PI genotypes were unavailable for two children. Seventy-eight percent of children without virologic suppression developed resistance mutations that impact second-line ART options. Only children who received RTV-based ART developed major PI-related resistance mutations, and use of this regimen should be avoided.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Antiretroviral Therapy, Highly Active / methods*
  • Cohort Studies
  • Drug Resistance, Viral*
  • Female
  • HIV Infections / drug therapy*
  • HIV Infections / virology*
  • HIV Protease / genetics*
  • HIV Protease Inhibitors / administration & dosage*
  • HIV Protease Inhibitors / pharmacology
  • HIV-1 / genetics*
  • HIV-1 / isolation & purification
  • Humans
  • Infant
  • Lopinavir / administration & dosage
  • Lopinavir / pharmacology
  • Male
  • Mutation, Missense
  • Nevirapine / administration & dosage
  • Nevirapine / pharmacology
  • RNA, Viral / blood
  • Ritonavir / administration & dosage
  • Ritonavir / pharmacology
  • Sequence Analysis, DNA
  • Südafrika
  • Viral Load
  • pol Gene Products, Human Immunodeficiency Virus / genetics

Substances

  • HIV Protease Inhibitors
  • RNA, Viral
  • pol Gene Products, Human Immunodeficiency Virus
  • Lopinavir
  • Nevirapine
  • HIV Protease
  • Ritonavir