CELL-SURFACE ANTIGEN EXPRESSION BY PERIPHERAL-BLOOD MONOCYTES IN ALLERGIC-ASTHMA - RESULTS OF 2.5 YEARS THERAPY WITH INHALED BECLOMETHASONEDIPROPIONATE
Wat. Slieker et al., CELL-SURFACE ANTIGEN EXPRESSION BY PERIPHERAL-BLOOD MONOCYTES IN ALLERGIC-ASTHMA - RESULTS OF 2.5 YEARS THERAPY WITH INHALED BECLOMETHASONEDIPROPIONATE, Mediators of inflammation, 5(5), 1996, pp. 362-369
AT present, inhaled glucocorticoids are widely accepted as the therapy
of choice in chronic asthma. Treatment with inhaled glucocorticoids s
ignificantly suppresses local airway inflammation in asthmatics, but m
ay also have systemic effects, e.g. a reduction of the number of circu
lating hypodense eosinophils or a down-modulation of HLA-DR antigen (A
g) expression by T lymphocytes in peripheral blood. However the effect
of long-term therapy with inhaled glucocorticoids on peripheral blood
monocytes (PBM), which are the precursors of the most numerous cell t
ype in the lung, the alveolar macrophage, have not yet been evaluated.
We therefore investigated the expression of various cell surface Ag o
n PBM from non-smoking patients with allergic asthma who were treated
for 2.5 years with a beta(2)-receptor agonist plus either an inhaled g
lucocorticoid (beclomethasone dipropionate, BDP) (n = 4) or an anticho
linergic or placebo (n = 8). We compared the results with healthy volu
nteers (n = 7). Long-term treatment of allergic asthmatics with inhale
d BDP, but not anticholinergic or placebo therapy, was associated with
a significantly lower CD11b Ag expression (p < 0.04) and higher expre
ssion of CD13, CD14 and CD18 Ag (p < 0.05, p < 0.02 and p < 0.04, resp
ectively) when com pared with the healthy control subjects (n = 7). Mo
st interestingly, PBM of asthmatics treated with inhaled BDP expressed
an almost two-fold higher level of CD14 Ag on their cell surface than
PBM of patients treated with anticholinergic or placebo (p < 0.03). N
o significant differences in the expression of CD16, CD23, CD25, CD32
and CD64 Ag or HLA-DR were observed between PBM from the different pat
ient groups or healthy controls. Taken together, this study shows that
long-term local therapy with inhaled BDP coincides with an altered ex
pression of at least one cell surface Ag on PBM from allergic asthmati
cs.