M. Fruhwirth et al., Flow-cytometric evaluation of oxidative burst in phagocytic cells of children with cystic fibrosis, INT A AL IM, 117(4), 1998, pp. 270-275
Objectives: The objective of this study was to assess the dye 2',7'-dichlor
ofluorescein (DCF assay in screening for alterations in polymorphonuclear c
ell (PMN) and monocyte (MC) oxidative burst of cystic fibrosis (CF) patient
s. Study design: 56 CF patients aged between 2 and 20 years were investigat
ed. Purified cells were stimulated with phorbolmyristate acetate: (PMA) and
zymosan (ZX). A range for DCF fluorescence for PMA- and ZX-stimulated and
non-stimulated cells was established based on data from 60 healthy controls
. Results: PMNs showed both enhancement and impairment. A deficient oxidati
ve burst was detected in a total of 14 CF patients caused by abnormally hig
h mean fluorescence intensity (MFl) of resting cells. Enhanced oxidative bu
rst was seen in 6 CF patients. CF patients responded differently to PMA or
ZX stimulation. Pseudomonas aeruginosa colonization significantly enhanced
(p<0.005) the MFI of resting PMNs. MCs of CF patients showed a significantl
y (p<0.05) enhanced oxidative burst after stimulation with PMA compared to
healthy controls, but no differences could be observed after stimulation wi
th ZX. Serum concentrations of interleukin-6 were elevated in all CF patien
ts, in particular in those with activation of both PMNs and MCs. Conclusion
: The DCF assay shows for the first time the heterogeneity of the oxidative
burst reaction in CF patients. In our opinion, the DCF assay is a reliable
method for detecting pathological oxidative burst in CF patients.