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Killing ofMycobacterium aviumby Neutrophils and Monocytes from AIDS Patients Treated with Recombinant Granulocyte‐Macrophage Colony‐Stimulating Factor
Author(s) -
Sandro Cinti,
Michael Coffey,
Amy Sullivan,
Powel Kazanjian
Publication year - 1999
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 - 10.1086/314851
Subject(s) - medicine , granulocyte macrophage colony stimulating factor , immunology , regimen , myalgia , granulocyte colony stimulating factor , colony stimulating factor , monocyte , azithromycin , granulocyte , microbiology and biotechnology , cytokine , biology , chemotherapy , antibiotics , haematopoiesis , stem cell , genetics
In this study, 30 AIDS patients without Mycobacterium avium infection were randomized to receive treatment with azithromycin (1200 mg), granulocyte-monocyte colony-stimulating factor (GM-CSF; 250 microg/m2/day for 5 days), or both agents. The M. avium killing capacity of neutrophils and monocytes harvested from each patient before intervention and during (day 4), and after therapy (day 8) was assessed. The mean virus load change in the groups receiving GM-CSF was +0.14 log human immunodeficiency virus RNA. After GM-CSF therapy, neither neutrophils nor monocytes could significantly reduce M. avium growth (P=.96 and.31, respectively). Bone pain, myalgia, presyncope, or fever occurred in 55% of patients receiving GM-CSF. Thus, the GM-CSF regimen used in this study did not affect virus load, frequently caused adverse reactions, and did not improve the M. avium killing capacity of neutrophils and monocytes. Future studies using a different GM-CSF regimen are indicated.

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