COMPLEMENTARY-DNA CLONING OF THE MAJOR ALLERGEN PHL-P-I FROM TIMOTHY GRASS (PHLEUM-PRATENSE) - RECOMBINANT PHL-P-I INHIBITS IGE BINDING TO GROUP-I ALLERGENS FROM 8 DIFFERENT GRASS SPECIES

Background: Grass pollens, such as pollen from timothy grass (Phleum p ratense), represent a major cause of type I allergy. Objective: In thi s report we attempted to determine how cross-reactive allergenic compo nents of grass pollens from different species can be represented by a minimum number of recombinant allergens. Methods: We isolated and sequ enced a timothy grass pollen cDNA coding for the major allergen Phl p I. A recombinant Phl p I-beta-galactosidase fusion protein, which boun d to IgE in 87% of patients with grass pollen allergy, was produced in Escherichia coil. Using recombinant Phl p V and Phl p I, we defined r epresentative patients' sera that bound to group I but not to group V allergens, as well as sera with reactivity against group I and group V allergens. IgE immunoblot inhibition studies were done with nitrocell ulose-blotted pollen extracts from eight grass species with different geographic distribution. Results: Preadsorption of patients' sera with recombinant nonfusion Phl p I strongly reduced IgE binding to group I allergens from the eight grasses, showing extensive cross-reactivity between species. Conclusion: A single recombinant group I allergen con tains many of the IgE epitopes of group I isoallergens from a number o f different grass species.