JAC Advance Access published online on November 18, 2002
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkf234
© 2002 by The British Society for Antimicrobial Chemotherapy
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Original Paper
1 Department of Pharmacy
Practice, Division of Infectious Diseases, University of Mississippi
Schools of Pharmacy and Medicine, Jackson, MS 39216-4505, USA; Department of Medicine, University of Mississippi
Schools of Pharmacy and Medicine, Jackson, MS 39216-4505, USA; Department of Microbiology, University of Mississippi
Schools of Pharmacy and Medicine, Jackson, MS 39216-4505, USA
* Corresponding author. E-mail: drogers{at}utmem.edu.
Received 15 April 2002
; revised 19 August 2002
; accepted 6 September 2002
Amphotericin B (AMB) is an antifungal agent that possesses
immunomodulatory properties that may contribute to its infusion-related
toxicity and activity. It has previously been shown to induce the
expression of genes encoding the cytokines interleukin (IL)-1
Differential expression of genes encoding immunomodulatory
proteins in response to amphotericin B in human mononuclear cells
identified by cDNA microarray analysis
2 Department of Medicine, University of Mississippi
Schools of Pharmacy and Medicine, Jackson, MS 39216-4505, USA
3 Department of Pharmacy
Practice, Division of Infectious Diseases, University of Mississippi
Schools of Pharmacy and Medicine, Jackson, MS 39216-4505, USA; Department of Medicine, University of Mississippi
Schools of Pharmacy and Medicine, Jackson, MS 39216-4505, USA
4 Department of Medicine, University of Mississippi
Schools of Pharmacy and Medicine, Jackson, MS 39216-4505, USA; Department of Microbiology, University of Mississippi
Schools of Pharmacy and Medicine, Jackson, MS 39216-4505, USA
and tumour necrosis factor (TNF)-
and the chemokines IL-8 and macrophage
inflammatory protein (MIP)-1
in the human
monocytic cell line THP-1. In an effort to identify additional AMB-responsive
genes, the gene expression profiles of both THP-1 cells and human
peripheral blood mononuclear cells (hPBMCs) on exposure to AMB were
assessed using cDNA microarray analysis. In addition to genes known
to be AMB responsive, we found the genes encoding IL-1
and
MIP-1
to be AMB responsive in both
THP-1 cells and hPBMCs. Increases in MIP-1
and
MIP-1
were also observed in the supernatants
of hPBMCs exposed to AMB. The expression of several genes in response
to AMB was unique to either cell type. Furthermore, variability
in gene expression in hPBMCs was observed between donors. These
genes and respective gene products may have significance in the
infusion-related toxicity and activity of AMB. ![]()
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