Tumour necrosis factor-alpha (TNF-alpha) and interleukin 1 beta (IL-1 beta)
have been implicated in the pathogenesis of asthma. The p38 kinase inhibit
or, SE 203580 inhibits TNF-alpha and IL-1 beta production in vitro and in v
ivo. In this study the effect of SE 203580 on allergen-induced airway TNF-a
production and inflammatory cell recruitment was investigated in sensitize
d Brown Norway rats. The allergen-induced increase in bronchoalveolar lavag
e (BAL) TNF-alpha was inhibited by SE 203580 at every dose tested (10-100 m
g kg(-1), p.o.). In contrast, neither ovalbumin-induced eosinophilia or neu
trophilia were inhibited by SE 203580 (10-100 mg kg(-1), p.o.). In conclusi
on, SE 203580 inhibits BAL TNF-alpha production by 95% without inhibiting e
ither antigen-induced airway eosinophilia or neutrophilia. This data sugges
ts that either the residual TNF-alpha is sufficent to drive allergen-induce
d inflammatory cell recruitment into the lung or that TNF-alpha is not invo
lved in allergen-induced inflammatory cell recruitment.