C. Estcourt et al., FLOW-CYTOMETRIC ASSESSMENT OF IN-VIVO CYTOKINE-PRODUCING MONOCYTES INHIV-INFECTED PATIENTS, Clinical immunology and immunopathology, 83(1), 1997, pp. 60-67
We have used two-color flow cytometry to study in vivo monocytic cytok
ine production at the single-cell level in HIV-infected patients. We d
emonstrated the presence of intracellular IL-1 alpha, IL-1 beta, IL-1r
a, and TNF alpha in circulating CD14(+) monocytes from HIV-infected pa
tients, The specificity of intracellular staining with anti-cytokine a
ntibodies was demonstrated by the suppression of the fluorescent signa
l when staining was performed in the presence of recombinant cytokines
. We did not detect any specific intracellular staining when anti-IL-4
antibodies were used since monocytes do not produce IL-4. In vivo int
racellular cytokine production of IL-1 alpha, IL-1 beta, IL-1ra, and T
NF alpha was higher in monocytes from HIV-infected individuals compare
d to monocytes from healthy controls; however, only the data concernin
g IL-1 alpha reached statistical significance. Monocytic cytokines are
involved in the regulation of HIV gene expression and may participate
in the modulation of the Th1/Th2 balance. The ability to follow the p
roduction of a wide range of cytokines by circulating monocytes of HIV
-infected patients should allow one to better analyze the role of mono
cytic cytokines in the pathogenesis of HIV disease. (C) 1997 Academic
Press.