The aim of this study was to investigate the susceptibility to T20 and the dynamics of amino acid changes in HR1 and HR2 of gp41 of HIV-1 obtained from plasma, peripheral blood mononuclear cells (PBMC), and primary isolates (PI) in four highly antiretroviral-experienced patients. These patients rece
Evolution of genotypic and phenotypic resistance to Enfuvirtide in HIV-infected patients experiencing prolonged virologic failure
✍ Scribed by Eva Poveda; Berta Rodés; Jean-Louis Labernardière; José Miguel Benito; Carlos Toro; Juan González-Lahoz; Jean-Louis Faudon; François Clavel; Jonathan Schapiro; Vincent Soriano
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 206 KB
- Volume
- 74
- Category
- Article
- ISSN
- 0146-6615
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Four heavily antiretroviral‐experienced HIV‐infected patients had significant plasma HIV‐RNA reductions (>1 log) after beginning an Enfuvirtide (ENF)‐based rescue regimen. However, all had viral rebound shortly thereafter, sustaining high levels of plasma viremia over 80 weeks. These patients developed rapidly genotypic and phenotypic resistance to ENF. Mutations within the HR1 env region were selected (N43D in three and G36V/D in one), resulting in high‐level phenotypic resistance to ENF. Interestingly, two patients had a sustained CD4+ T‐cell increase and two maintained stable CD4+ T‐cell counts despite virologic failure under ENF. The possible mechanisms involved in this response were examined. Changes in virus tropism from R5 to R5/X4 were observed in two patients, in parallel with increases in ENF phenotypic resistance. Low levels of T‐cell activation, T‐cell turnover, and cytotoxic T lymphocyte (CTL) activity were found in all four patients. An overall increase in the proportion of viruses released from cells of the macrophage lineage was observed. In summary, single mutations at the HR1 env region result in significant loss of susceptibility to ENF. Despite virologic failure, these patients may maintain elevated CD4+ counts through a reduction in their overall immune activation. J. Med. Virol. 74:21–28, 2004. © 2004 Wiley‐Liss, Inc.
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