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The insulin B chain residues 9 through 23 form a critical autoantigenic peptide recognized by pathogenic CD4+ T cells. This region's presentation by MHC class II molecules initiates autoimmune destruction characteristic of type 1 diabetes. Hybrid peptides containing portions of this sequence fused with other proteins may enhance its antigenicity. It is not a direct drug target, but rather an epitope for immunotherapy.
Not applicable (as a target). Therapeutic strategies aim to modulate immune responses to this epitope via altered peptide ligands or tolerogenic administration.
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