R. Valenta et al., RECOMBINANT ALLERGEN-SPECIFIC ANTIBODY FRAGMENTS - TOOLS FOR DIAGNOSIS, PREVENTION AND THERAPY OF TYPE-I ALLERGY, Biological chemistry, 378(8), 1997, pp. 745-749
Type I allergy represents a hypersensitivity occurring in almost 20% o
f the population that is based on the recognition of innocuous airborn
antigens (pollen, mite, mould and pet allergens) by specific immunogl
obulin E. Allergic symptoms (e.g. allergic rhinitis, conjunctivitis, a
sthma) are caused by the release of biological mediators from effector
-cells after allergen-induced crosslink of receptor-bound IgE, Here we
discuss strategies to obtain recombinant allergen-specific antibody f
ragments (Fabs) from mouse and human cell lines as well as directly fr
om allergic patients lymphocytes via the combinatorial library technol
ogy. It is suggested to use recombinant allergen-specific Fabs for the
standardization of allergen extracts currently used for diagnosis and
treatment, to determine allergen contents in allergen sources and the
environment to allow preventive measures and to use allergen-specific
Fabs as therapeutic tools to interfere with the allergen-IgE interact
ion. The latter appears possible because IgE represents the least abun
dant class of immunoglobulins and there is increasing evidence for a l
imited diversity among allergens and their B-cell epitopes, Moreover,
allergic effector reactions are mostly confined to accessible target o
rgans so that a local application of competing Fabs prior to allergen
exposure might represent a feasible therapeutic approach.