Altered antigenicity of M-177, a 177-kDa allergen from the house dust miteDermatophagoides farinae, in stored extract

Citation
A. Fujikawa et al., Altered antigenicity of M-177, a 177-kDa allergen from the house dust miteDermatophagoides farinae, in stored extract, CLIN EXP AL, 28(12), 1998, pp. 1549-1558
Citations number
20
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Immunology
Journal title
CLINICAL AND EXPERIMENTAL ALLERGY
ISSN journal
09547894 → ACNP
Volume
28
Issue
12
Year of publication
1998
Pages
1549 - 1558
Database
ISI
SICI code
0954-7894(199812)28:12<1549:AAOMA1>2.0.ZU;2-V
Abstract
Background A high molecular weight allergen, M-177 (177 kDa) was isolated f rom Dermatophagoides farinae using a specific antibody raised to an allerge nic clone Mag 3, which was obtained by immunoscreening a mite cDNA library. The potent IgE reactivity of M-177 is comparable with that of Der f 2. Objective The aim of this study was to analyse the molecular characteristic s and the allergenic activity of M-177 in stored mite extracts. Methods Antigens were analysed by immunoblotting and enzyme-linked immunoso rbent assay (ELISA; inhibition). Allergenic activity was estimated from IgE reactivity and the results of a histamine release assay. Results The intact M-177 molecule was present in high concentrations in fre sh extract obtained from purified mite bodies, but was only detected in sma ll amounts in stored extracts. Instead of the intact molecule, anti-Mag 3 a ntibody detected various cross-reactive antigens in the stored preparations . Studies of a stored liquid extract showed that these cross-reactive antig ens were produced by the degradation of M-177, and that this change was sup pressed by the addition of protease inhibitors. Interestingly, the allergen ic activity of the fragmented M-177 (sM-177) isolated from the stored extra cts was greater than that of the intact antigen. Specific IEE reacted with sM-177 in 84.2% of 38 sera samples from patients allergic to mites, while 6 5.8% were positive for M-177-specific IgE. Similarly, the histamine release test showed that sM-177 had greater allergenic activity in vitro. ELISA in hibition indicated that the increased allergenic activity resulted from alt eration of the antigenicity with the degradation of M-177. Conclusions M-177 is a protease-sensitive allergen. The breakdown products of M-177 provoked higher allergenic activity than the intact allergen.