Immunomodulatory Treatment of Mycobacterium avium Complex Bacteremia in Patients with AIDS by Use of Recombinant Granulocyte-Macrophage Colony-Stimulating Factor
Author(s) -
Carol A. Kemper,
Luiz E. Bermudez,
Stan Deresinski
Publication year - 1998
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/515249
Subject(s) - bacteremia , medicine , azithromycin , superoxide , granulocyte , monocyte , immunology , granulocyte macrophage colony stimulating factor , macrophage , sepsis , granulocyte colony stimulating factor , microbiology and biotechnology , cytokine , in vitro , biology , antibiotics , chemotherapy , biochemistry , enzyme
Eight AIDS patients with Mycobacterium avium complex (MAC) bacteremia were randomized to receive azithromycin with or without granulocyte-macrophage colony-stimulating factor (GM-CSF) for 6 weeks to examine the effect of GM-CSF administration on clearance of mycobacteremia and on monocyte function. Superoxide anion production was significantly increased ex vivo in monocytes from patients receiving GM-CSF but not in those from patients receiving azithromycin alone. Relative to monocytes obtained from untreated healthy controls, median differences in viable intracellular MAC at 2, 4, and 6 weeks were -0.76, -0.94, and -0.47 log10 cfu/mL of lysate for cells from patients receiving GM-CSF versus -0.15, -0.11, and -0.19 log10 cfu/mL for cells from patients receiving azithromycin alone. Although no effect on mycobacteremia was detected, the administration of GM-CSF to AIDS patients with MAC bacteremia resulted in activation of their blood monocytes, as evidenced by increased superoxide anion production and enhanced mycobactericidal activity. GM-CSF deserves further investigation in the treatment of mycobacterial infections.
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