The clinical utility of a flow cytometric assay (FCA) for intracellular HIV p24 antigen was evaluated in a group of HIV-1-infected subjects. A previously described method, p24-FCA (1), was modified to minimize nonspecific staining and to include irrelevant isotype-matched control antibodies. Blood m
Cell cycle distribution of CD4+ lymphocytes in HIV-1-infected subjects
✍ Scribed by Chaves, Mariana Melillo Sauer ;Kallas, Esper Georges
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 221 KB
- Volume
- 62B
- Category
- Article
- ISSN
- 0196-4763
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Background
Apoptosis is one of the possible explanations for the progressive loss of CD4^+^ T lymphocytes in infection with the human immunodeficiency virus (HIV), which may interfere with cell cycle distribution. This study evaluated the cell cycle of CD4^+^ and CD8^+^ lymphocytes in HIV‐infected subjects and controls.
Methods
Two methods to identify lymphocytes for cell cycle analysis were evaluated, magnetic beads and concurrent staining, and both were followed by propidium iodide DNA labeling. The chosen method was used to evaluate the cell cycle of lymphocytes in HIV‐1–infected subjects and controls.
Results
There was no significant difference between the two methods, although a higher variability was observed with the magnetic bead cell separation method. A higher proportion of cells in the S phase was observed in HIV‐1 patients (2.69% vs. 1.19%, P = 0.016), coupled with a decrease in G~1~ (96.11% vs. 98.10%, P = 0.005) in CD4^+^ lymphocytes, a phenomenon not observed in CD8^+^ lymphocytes. No correlation was detected between the different cell cycle phases and T‐lymphocyte counts or viral load.
Conclusions
The present work developed a new approach to evaluate lymphocyte cell cycle distribution, applied in the setting of HIV‐1 infection. It may contribute to the understanding of the CD4^+^ T‐lymphocytes depletion seen in these patients. © 2004 Wiley‐Liss, Inc.
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