Granulocyte Colony-Stimulating Factor Increases CD4+ T Cell Counts of Human Immunodeficiency Virus-Infected Patients Receiving Stable, Highly Active Antiretroviral Therapy: Results from a Randomized, Placebo-Controlled Trial
Thirty human immunodeficiency virus (HIV)-infected patients with CD4+ T cell counts <350 cells/mm3 who had received stable, highly active antiretroviral therapy (HAART) for at least 24 weeks were randomized to receive either placebo or granulocyte colony-stimulating factor (G-CSF; 0.3 mg/mL 3 tim...
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Published in | The Journal of infectious diseases Vol. 181; no. 3; pp. 1148 - 1152 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
University Chicago Press
01.03.2000
University of Chicago Press |
Subjects | |
Online Access | Get full text |
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Summary: | Thirty human immunodeficiency virus (HIV)-infected patients with CD4+ T cell counts <350 cells/mm3 who had received stable, highly active antiretroviral therapy (HAART) for at least 24 weeks were randomized to receive either placebo or granulocyte colony-stimulating factor (G-CSF; 0.3 mg/mL 3 times a week) for 12 weeks. Blood samples were collected at specified time points. G-CSF treatment enhanced the total lymphocyte count (P = .002) and increased CD3+ (P = .005), CD4+ (P = .03), and CD8+ (P = .004) T cell counts as well as numbers of CD3− CD16+CD56+ NK cells (P = .001). The increases in CD4+ and CD8+ cell counts resulted from increases in CD45RO+ memory T cells and cells expressing the CD38 activation marker. Lymphocyte proliferative responses to phytohemagglutinin and Candida antigen decreased, whereas NK cell activity and plasma HIV RNA did not change during G-CSF treatment. After 24 weeks, all immune parameters had returned to baseline values. This study suggests that G-CSF treatment of HIV-infected patients receiving stable HAART increases the concentration of CD4+, CD8+, and NK cells without inducing changes in the virus load. |
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Bibliography: | istex:B58288830A7943AF28F809E889746ED7D61CD2C2 ark:/67375/HXZ-JBQXXT2J-Q |
ISSN: | 0022-1899 1537-6613 |
DOI: | 10.1086/315305 |