Rl. Shields et al., INHIBITION OF ALLERGIC REACTIONS WITH ANTIBODIES TO IGE, International archives of allergy and immunology, 107(1-3), 1995, pp. 308-312
Numerous clinical studies show that direct interference with the IgE r
esponse leads to a decrease or elimination of allergic symptoms. The a
im of these studies was to design a therapy aimed at decreasing IgE le
vels in order to ameliorate atopic disease. To this end, a murine mono
clonal antibody, MAE11, directed against IgE was identified, which had
all the properties necessary to interfere with IgE responses, but lac
ked the harmful side effects of inducing receptor cross-linking. The a
ntibody was selected on the basis of its ability to bind circulating I
gE at the same site as the high-affinity receptor, thus blocking the b
inding of IgE to mast cells and basophils. To allow for possible chron
ic administration and to avoid the problems of antigenicity, MAE11 as
humanized. The best of several humanized variants, version 25 (rhumAb-
E25) was selected since it possessed binding affinity and biological a
ctivity comparable to MAE11. Clinical studies are underway to determin
e the safety and efficacy of this treatment for allergic rhinitis and
asthma.