LEUKOTRIENE B-4 AND C-4 GENERATION BY HUMAN-LEUKOCYTES AFTER EX-VIVO STIMULATION WITH CA-IONOPHORE AND OPSONIZED ZYMOSAN IN CHILDREN WITH ATOPIC ASTHMA
S. Kristjansson et al., LEUKOTRIENE B-4 AND C-4 GENERATION BY HUMAN-LEUKOCYTES AFTER EX-VIVO STIMULATION WITH CA-IONOPHORE AND OPSONIZED ZYMOSAN IN CHILDREN WITH ATOPIC ASTHMA, Pediatric allergy and immunology, 6(3), 1995, pp. 155-160
The ex vivo release of leukotriene B-4 (LTB(4)) and leukotriene C-4 (L
TC(4)) from leukocytes was evaluated after stimulation with both Ca-io
nophore (Ca-I) and opsonized zymosan (OZ) in children with atopic asth
ma. Twenty-seven patients with asthma of varying severity were evaluat
ed and divided into three groups: 1) moderate to severe asthma using i
nhaled steroids and symptom-free for the last 3 weeks (n = 8), 2) mild
asthma with sporadic symptoms, only using inhaled beta(2)-agonists <
3 times/week (n = 8), and 3) acute asthmatic attacks admitted to hospi
tal (n = 11). A group of children without atopic disease or any other
known disease served as controls (n = 15). Total serum IgE levels were
significantly increased in the children with asthma compared with the
control group. LTC(4) production was only significantly increased in
the group of children with moderate to severe asthma after stimulation
with Ca-I, when compared with controls. In the same group, a trend to
wards increased LTC(4) production after stimulation with OZ was found.
LTB(4) was not significantly increased in any patient group compared
with the control group. A significant correlation between LTC(4) produ
ction after stimulation with Ca-I, but not OZ, and the relative blood
eosinophil count was found in all subjects. LTC(4) generation per eosi
nophilic cell after stimulation with Ca-I or OZ was not statistically
different in any patient group compared with the controls. We conclude
that the increased leukotriene (LT) levels found after the stimulatio
n of peripheral white blood cells sampled from atopic children with as
thma are mainly the result of increased numbers of LT-producing cells,
rather than due to increased releasability from these cells.