The beneficial effects of inhaled corticosteroids in the treatment of asthm
a are well established. A potent topical anti-inflammatory action is assume
d to underlie the therapeutic effect, given that these agents alter the num
ber and function of a range of inflammatory cells and markers in airway bio
psies. This activity profile is shown by all inhaled corticosteroids, in a
variety of patient types and study designs. Thus, treatment with inhaled co
rticosteroids leads to consistent reductions in the number and activation o
f mast cells and eosinophils in biopsy specimens. Other relevant findings i
nclude reductions in T-lymphocytes, which contribute to chronic inflammatio
n via the secretion of pro-inflammatory cytokines (some of which are respon
sible for eosinophil accumulation and activation). Inhaled corticosteroids
may therefore act by down-regulating immunoreactivity, so reducing activati
on of T lymphocytes and (consequently) eosinophils. There is considerable i
nterest in whether corticosteroids can inhibit or reverse some structural c
hanges in the airways, including basement membrane thickening, collagen dep
osition and increased airway vascularity; it has been suggested that these
changes may contribute towards airway hyperresponsiveness and irreversible
airway obstruction. In summary, inhaled corticosteroids have a broad spectr
um of antiinflammatory activity in asthma patients, but the relationship be
tween changes in clinical and immunopathological parameters, particularly i
n the long-term, requires further study.