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 inThe Journal of infectious diseases Vol. 181; no. 3; pp. 1148 - 1152
Main Authors Aladdin, Hassan, Ullum, Henrik, Nielsen, Susanne Dam, Espersen, Christina, Mathiesen, Lars, Katzenstein, Terese L., Gerstoft, Jan, Skinhoj, Peter, Pedersen, Bente Klarlund
Format Journal Article
LanguageEnglish
Published United States University Chicago Press 01.03.2000
University of Chicago Press
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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.
Bibliography:istex:B58288830A7943AF28F809E889746ED7D61CD2C2
ark:/67375/HXZ-JBQXXT2J-Q
ISSN:0022-1899
1537-6613
DOI:10.1086/315305