Hypoallergenic acid-sensitive modification preserves major mugwort allergen fold and delivers full repertoire of MHC class II-binding peptides during endolysosomal degradation. Issue 91 (15th September 2016)

• Record Type: Journal Article
• Authors: Stanic-Vucinic, Dragana; Stojadinovic, Marija; Mirkov, Ivana; Apostolovic, Danijela; Burazer, Lidija; Atanaskovic-Markovic, Marina; Kataranovski, Milena; Cirkovic Velickovic, Tanja
• Is Part Of: RSC advances. Volume 6:Issue 91(2016)
• Page Start: 88216
• Page End: 88228
• Publication Date: 2016-09-15
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c6ra17261j
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Hypoallergenic acid-sensitive modification preserves major mugwort pollen allergen fold and delivers a full repertoire of MHC class II-binding peptides during endolysosomal degradation. Abstract : Modified allergens are a safer and more efficient alternative to natural allergens for specific immunotherapy. As the modification of an allergen can diminish its immunogenicity due to the alteration of T-cell epitopes, in this paper we study the effects of a reversible chemical modification of Art v 1, the main allergen of mugwort pollen, on its allergenicity and immunogenicity. Modification of Art v 1 by cis -aconitylation into a polyanionic derivative (CAA) did not result in any significant structural alteration. However, IgE-binding epitopes on CAA were blocked, resulting in a reduced IgE-binding and basophil activation. Both proteins induced proliferation of CD3 + CD4 + T-cells in mugwort-allergic patients, but only unmodified allergens increased IL-4, IL-5 and IL-10 production. Rabbit and mouse anti-CAA antibodies exhibited cross-reactivity with native allergens and blocked human IgE-binding to Art v 1. Degradation of CAA by lysosomal fraction enzymes resulted in a similar set of peptides, harboring MHC class II-binding peptides, as unmodified proteins. Thus, cis -aconitylation modified Art v 1 had a significantly reduced allergenicity, whereas its immunogenicity was completely preserved. Acid-environment-responsive modification, which releases a full repertoire of native allergen epitopes within a particular site, can be considered a smart drug delivery system, which is able to deliver a therapeutically-effective dose in a controlled manner, and minimizes adverse side effects.