Long-term follow-up of patients taking tenofovir DF with low-level HIV-1 viremia and the K65R substitution in HIV-1 RT

AIDS. 2007 Mar 30;21(6):761-3. doi: 10.1097/QAD.0b013e3280187533.

Abstract

Patients with on-going HIV-1 replication and a K65R mutation in HIV-1 RT were assessed for further development of RT mutations while taking tenofovir disoproxil fumarate and other antiretroviral drugs. K65R was observed in 10 out of 536 treatment-experienced patients entering the study. K65R became undetectable in two patients, and the development of additional resistance mutations was minimal. Over 18 months, no patient developed multinucleoside resistance (Q151M or T69 insertions) and plasma viral loads were stable (median +0.04 log10 copies/ml).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine / analogs & derivatives*
  • Adenine / therapeutic use
  • Anti-HIV Agents / therapeutic use
  • Anti-Retroviral Agents / therapeutic use*
  • Drug Resistance, Viral / genetics
  • Drug Therapy, Combination
  • HIV Infections / drug therapy*
  • HIV Infections / virology
  • HIV-1 / enzymology
  • HIV-1 / genetics*
  • Humans
  • Long-Term Care
  • Longitudinal Studies
  • Mutation
  • Organophosphonates / therapeutic use*
  • RNA, Viral / blood
  • RNA-Directed DNA Polymerase / genetics*
  • Reverse Transcriptase Inhibitors / therapeutic use
  • Tenofovir
  • Treatment Outcome
  • Viral Load

Substances

  • Anti-HIV Agents
  • Anti-Retroviral Agents
  • Organophosphonates
  • RNA, Viral
  • Reverse Transcriptase Inhibitors
  • Tenofovir
  • RNA-Directed DNA Polymerase
  • Adenine