Long before the discovery of IgE it was reported that human dander extract
can elicit immediate-type skin reactions in patients with severe atopy and
that this skin sensitivity can be passively transferred with serum, Several
recent findings have rekindled the interest in this phenomenon and led to
the concept that IgE autoreactivity may play a pathogenetic role in severe
and chronic forms of atopy, The elucidation of the nature of several enviro
nmental allergens has revealed striking structural and immunologic similari
ties with human proteins. It was also reported that patients predominantly
with severe and chronic manifestations of atopy (eg, atopic dermatitis) con
tain IgE autoantibodies against a wide variety of proteins expressed in his
togenetically unrelated human cell types and tissue specimens, Last, comple
mentary DNAs coding for autoallergens were isolated from human expression c
omplementary DNA libraries and recombinant autoallergens were produced. The
autoallergens characterized to date represent mainly intracellular protein
s, but some of them could be detected as IgE immune complexes in sera of se
nsitized patients. We suggest that at least two pathomechanisms could play
a role in autoallergy, First, autoallergens may cross-link effector cell-bo
und IgE autoantibodies and, by release of inflammatory mediators, lead to i
mmediate-type symptoms. Second, IgE-mediated presentation of autoallergens
may activate autoreactive T cells to release proinflammatory cytokines, con
tributing to the magnitude of the allergic tissue reaction.