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House dust mite (HDM) allergen extract, derived from the species Dermatophagoides pteronyssinus and Dermatophagoides farinae, is the primary therapeutic agent used in allergen-specific immunotherapy (AIT) for dust mite allergies [1]. These extracts contain a complex mixture of proteins, most notably the Group 1 (cysteine proteases) and Group 2 (NPC2 family) allergens, which are the major triggers for IgE-mediated hypersensitivity [3]. In sensitized individuals, these allergens cross-link IgE on mast cells and basophils, leading to the release of inflammatory mediators that cause symptoms of allergic rhinitis and asthma [4]. Therapeutic administration of these allergens, either subcutaneously or sublingually, works by inducing immunological tolerance. This process involves the expansion of regulatory T-cells (Tregs), a shift from a Th2 to a Th1 cytokine profile, and the induction of blocking antibodies such as IgG4, which compete with IgE for allergen binding [2, 4]. Consequently, the immune system becomes less reactive to environmental exposure, providing long-term clinical benefits and potentially preventing the progression from rhinitis to asthma [1, 2].
Induction of immune tolerance through repeated exposure, leading to a shift from Th2 to Th1/Treg responses, increased production of allergen-specific IgG4, and decreased IgE-mediated mast cell degranulation [2, 4].
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