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This entry is not a single molecular target such as a receptor or enzyme, but a biological process describing the modulation of T cell responses specific to allergens. This modulation is accomplished by several cell types and mechanisms, notably by the induction of allergen-specific regulatory T cells (Tregs) that secrete regulatory cytokines IL-10 and TGF-β, thereby suppressing pro-inflammatory T cell responses (Th2, Th1) and contributing to peripheral immune tolerance[2]. B cells also play a key role in downregulating allergen-specific CD4^+^ T cell responses, primarily through regulatory cytokines and antigen presentation[1]. Successful allergen-specific immunotherapy leverages this pathway, leading to clinical improvement by reducing allergic inflammation and symptoms. However, this is a functional immune process, not an individual molecular entity[1][2]. **Key point:** This "target" is a process involving multiple molecular actors (Tregs, B cells, cytokines) and not a canonical receptor or drug target, thus is_incorrect = true for the requested structured information format.
Induction of allergen-specific regulatory T cells (Treg) that secrete IL-10 and TGF-β, suppressing effector T cell (Th1, Th2, Th17) activity[2] Skewing of T cells from a pro-inflammatory (Th2/Th1) phenotype to a regulatory phenotype[2] Suppression via B-cell–dependent presentation and modulation (through regulatory cytokine production)[1] Blocking IgE activation via IgG4/IgG1 induction[2]
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