Early archiving and predominance of nonnucleoside reverse transcriptase inhibitor-resistant HIV-1 among recently infected infants born in the United States

J Infect Dis. 2007 May 15;195(10):1402-10. doi: 10.1086/513871. Epub 2007 Apr 5.

Abstract

Background: The extent to which drug-resistant human immunodeficiency virus type 1 (HIV-1) acquired through mother-to-child transmission (MTCT) or failed chemoprophylaxis populates viral reservoirs and limits responses to antiretroviral treatment in infants is unknown.

Methods: We evaluated the presence, type, and persistence of drug-resistant HIV-1 in pretreatment plasma and resting CD4(+) T cells from US infants enrolled in a multicenter, open-label, phase 1/2 treatment trial of lopinavir/ritonavir (Pediatric AIDS Clinical Trials Group Protocol 1030) in young infants.

Results: Twenty-two consecutively enrolled infants initiating highly active antiretroviral therapy at a median age of 9.7 weeks and treated for up to 96 weeks were studied. Drug-resistant HIV-1 was present in 5 (23.8%) of 21 infants analyzed; 4 (80.0%) had nonnucleoside reverse transcriptase inhibitor (NNRTI)-resistant HIV-1, only 1 of whom had a history of receiving nevirapine chemoprophylaxis. All 4 infants had NNRTI-resistant variants other than the K103N mutation. The fifth infant had the M184V mutation. Drug-resistant virus was archived in the resting CD4(+) T cell latent reservoir in all 5 infants.

Conclusions: The high rate, types, and early archiving of drug-resistant HIV-1 suggests that resistance testing be considered for infants, especially when an NNRTI-based regimen is planned. Furthermore, drug-resistance outcomes in infants should be an important secondary end point in MTCT trials.

Trial registration: ClinicalTrials.gov NCT00038480.

Publication types

  • Clinical Trial, Phase I
  • Clinical Trial, Phase II
  • Multicenter Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acquired Immunodeficiency Syndrome / drug therapy*
  • Acquired Immunodeficiency Syndrome / immunology
  • Anti-HIV Agents / therapeutic use
  • Anti-HIV Agents / toxicity
  • Antiretroviral Therapy, Highly Active
  • CD4 Lymphocyte Count
  • DNA, Complementary / genetics
  • Drug Resistance, Viral*
  • HIV-1 / drug effects*
  • Humans
  • Infant
  • Lopinavir
  • Male
  • Pyrimidinones / therapeutic use
  • Pyrimidinones / toxicity
  • RNA, Viral / blood
  • Reverse Transcriptase Inhibitors / therapeutic use*
  • Reverse Transcriptase Inhibitors / toxicity
  • Reverse Transcriptase Polymerase Chain Reaction
  • Ritonavir / therapeutic use
  • Ritonavir / toxicity
  • United States
  • Viral Load
  • Zidovudine / therapeutic use
  • Zidovudine / toxicity

Substances

  • Anti-HIV Agents
  • DNA, Complementary
  • Pyrimidinones
  • RNA, Viral
  • Reverse Transcriptase Inhibitors
  • Lopinavir
  • Zidovudine
  • Ritonavir

Associated data

  • ClinicalTrials.gov/NCT00038480