T lymphocytes present in allergically inflamed tissue synthesize and s
ecrete the cytokines IL-3, IL-4, IL-5 and GM-CSF which may act as chem
otaxins on eosinophils. In contrast to the former cytokines, IL-4 is c
hemotactic only for eosinophils from peripheral blood of patients with
atopic dermatitis and not for eosinophils from normal individuals. IL
-4 has the same chemotactic potency as the other cytokines. The optima
l chemotactic potency is reached at a concentration of 10 nM. In contr
ast, neutrophils do not respond chemotactically to IL-4. Checkerboard
analysis, inhibition studies with monoclonal anti-IL-4. Abs and desens
itization experiments indicated specific interaction of IL-4 with eosi
nophils. In eosinophils from normal individuals, IL-4 responsiveness c
ould be induced by pretreatment of the cells with IL-5 and GM-CSF. In
addition to the fact that IL-4 may be responsible for selective eosino
phil transendothelial migration, IL-4 may exert an important modulator
y mode of action on eosinophil migration and function within allergica
lly inflamed tissue. Our findings suggest the presence of a functional
IL-4R on eosinophils from atopic dermatitis patients.