Co-expression of CXCR4/fusin and galactosylceramide in the human intestinal epithelial cell line HT-29

O Delézay, N Koch, N Yahi, D Hammache, C Tourres… - Aids, 1997 - journals.lww.com
O Delézay, N Koch, N Yahi, D Hammache, C Tourres, C Tamalet, J Fantini
Aids, 1997journals.lww.com
Objectives: To study the kinetics of plasma viraemia and HIV-infected lymph-node cells in
stable asymptomatic HIV infection with high CD4+ T-cell counts. Methods: Nine
asymptomatic HIV-infected patients with stable CD4+ T-cell counts (510–1350× 10 6/l) were
treated with a triple-drug combination. Plasma viraemia was determined at days 0, 3, 7, 10,
14, 21 and 28 of treatment [Roche polymerase chain reaction (PCR) and ultrasensitive PCR
assay]. Sequential lymph-node biopsies were examined in four patients before and after 4 …
Abstract
Objectives:
To study the kinetics of plasma viraemia and HIV-infected lymph-node cells in stable asymptomatic HIV infection with high CD4+ T-cell counts.
Methods:
Nine asymptomatic HIV-infected patients with stable CD4+ T-cell counts (510–1350× 10 6/l) were treated with a triple-drug combination. Plasma viraemia was determined at days 0, 3, 7, 10, 14, 21 and 28 of treatment [Roche polymerase chain reaction (PCR) and ultrasensitive PCR assay]. Sequential lymph-node biopsies were examined in four patients before and after 4 weeks of treatment. Productively infected cells were counted in lymph-node sections (in situ hybridization). The infection rates of FACS-sorted CD4+ lymph-node T cells and the expression of single-spliced, double-spliced and full-length HIV transcripts were determined.
Results:
HIV plasma RNA half-lives ranged from 1.4 to 2.7 days. Viral turnover varied between 0.07 and 7.54× 10 8 copies per day. The number of productively infected lymph-node cells as well as the amount of extracellular virus in germinal centres was markedly reduced during treatment, paralleled by a clearance of single-spliced, double-spliced and full-length HIV transcripts from CD4+ lymph-node T cells. Plasma viraemia remained detectable with an ultrasensitive PCR assay in three out of four patients. The percentage of lymph-node CD4+ T cells harbouring proviral DNA decreased only slightly.
Conclusions:
The kinetics of HIV replication are rapid in stable asymptomatic infection, and the magnitude of replication varies considerably. Productively infected lymph-node cells and extracellular virus in germinal centres undergo a rapid turnover, whereas latently infected CD4+ T cells have a lower rate of turnover. The latter may contribute substantially to viral persistence during therapy.
Lippincott Williams & Wilkins