A great variety of recombinant plant, mite, mold, mammal, and insect a
llergens have been expressed in heterologous hosts (e.g., Escherichia
coli), their cDNA being used as a template. The number of biologically
active recombinant allergens available for experimental, diagnostic,
and therapeutic purposes is increasing tremendously. Recombinant aller
gens have proven to be valuable tools to investigate T-cell and B-cell
recognition of allergens as well as to study mechanisms of specific I
gE regulation. The immunologic equivalence of many relevant recombinan
t allergens with their natural counterparts has been demonstrated, and
the three-dimensional structures of several recombinant allergens hav
e been described recently. As a result of extensive cross-reactivities
among the relevant allergens, it appears that the number of epitopes
needed for diagnosis and specific immunotherapy is less diverse than o
riginally anticipated and might be soon covered by recombinant molecul
es. Recombinant allergens have been used for successful in vitro, as w
ell as in vivo, allergy diagnosis, and work is in progress to produce
recombinant allergen derivatives with reduced anaphylactic potential t
o improve current forms of immunotherapy.