Techniques of generic engineering applied to allergens have enabled the pro
duction of recombinant allergens. The validation of recombinant allergens i
mplies that their immunological activity and their identity with natural al
lergens might be confirmed by in vitro and in vivo techniques carried out o
n a sufficiently large number of allergic subjects. Currently available res
ults for the principal pneumoallergens are reported. Thus the work of valid
ating recombinant allergen BeTv1 has been confirmed by in vitro tests and a
lso by skin tests and nasal and bronchial provocation tests. The associatio
n of four recombinant allergens of phleole has enabled the detection in vit
ro of sensitisation to germinated pollens in 94.5% of patients. For mites t
he validity of group 2 recombinant allergens has been confirmed. A system e
nabling the expression of glycosylation of recombinant proteins was necessa
ry to validate recombinant proteins in group 1 allergens. The recombinant a
llergen Blot5 is recognised as bring effective in the detection of sensitiz
ation to Blomia tropicalis, a domestic allergen in sub tropical countries.
The recombinant allergens Bla g 4 and Bla g 5 have been tested in vitro and
in vivo and reactions were positive in nearly 50% of subjects sensitive to
cockroaches. The recombinant Asp f 1 has been tested in subjects suffering
from allergic bronchopulmonary aspergillosis and is positive in 60-85% of
cases.
Some studies are available for recombinant allergens of certain animal anti
gens (Equ c 1, Bos d 2). The consequences of clarifying recombinant allerge
ns are then analysed : obtaining better standardised allergens for diagnost
ic tests, studying the spectrum of specificities of IgE induced by an aller
gen, the quantification of specific IgE, a better approach to mixed allergi
es with the help of recombinant allergens of the principal mixed allergens.
Some recent progress has led to the production of modified recombinant all
ergens: the synthesis of recombinant polypeptides corresponding to T epitop
es, the production of isoform recombinant allergens with reduced allergenic
activity, the production of recombinant allergens of modified allergenic m
olecules by directed mutations and the production of recombinant fragments
of allergenic molecules. The use of modified recombinant allergens is a way
of permitting research which would, in the future, lead to new modalities
of specific immunotherapy.