The concentration of circulating IgE is sufficiently low for administration
of carefully selected anti-IgE antibodies to trap IgE and block its intera
ctions with receptors. Anti-IgE antibodies targeted against the interaction
motif of IgE and the type I receptor (Fc epsilon RT) are devoid of any ana
phylactic effects, as they cannot access IgE bound by receptors. These non-
anaphylactogenic antibodies have been modified to reduce murine Ige sequenc
es (chimeric antibody or humanized antibody) to a minimum. Tested in precli
nical and clinical trials, they reduce the quantity of free IgE available t
o sensitize target cells and exert an inhibitory effect on immediate and de
layed allergic bronchospastic responses. They also reduce (Fc epsilon RI) e
xpression by circulating basophils and consequently their activation potent
ial gy specific IgE, The long-term effects of anti-IgE antibodies on allerg
ic reactions and IgE production have yet to be evaluated.