Polymerized allergens (allergoids) have been introduced in the immunot
herapy of allergic disease in order to reduce the risk of side effects
. However, their high molecular weight can be a limit, particularly wh
en they are administered by a route involving passage through the muco
sal barrier. We describe a simple procedure aimed at developing an ori
ginal modified allergen with significantly less allergenic potential (
intended as human IgE-binding capacity) but preserving the monomeric n
ature of the molecule. Par j I, the major allergen of Parietaria judai
ca pollen, was purified by a combination of monoclonal antibodies and
affinity chromatography. Par j I allergen was then modified by reactio
n with potassium cyanate (KCNO), and compared with the native allergen
to evaluate its allergenic potency (RAST-inhibition) and molecular we
ight (SDS-PAGE). Modified allergen showed significantly lower allergen
ic potency but kept its original molecular weight, making it particula
rly suitable for buccal (sublingual) administration. To study the adso
rption profile, modified Par j I was radiolabeled and administered int
ravenously and sublingually to normal rats. The prospects for clinical
application of the modified allergen are discussed.