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IgD-Fc-Ig is a **recombinant fusion protein** composed of the Fc region of human Immunoglobulin D (IgD) linked to the Fc region of human IgG1. It acts as a selective blocker of the interaction between IgD and its receptor (IgDR, also called FcδR), thereby inhibiting the downstream signaling that drives abnormal T cell and B cell proliferation and activation. IgD-Fc-Ig was designed to reduce the pathological immune activation seen in autoimmune diseases such as rheumatoid arthritis and systemic lupus erythematosus, as well as certain malignancies like T-cell acute lymphoblastic leukemia. Preclinical and animal model data indicate it may restore immune balance by suppressing Th17 cell development and restoring Th17/Treg cell ratios. Its mechanism leverages prolonged half-life (from the IgG1-Fc domain) and reduced immunogenicity through selective targeting and blockade of the IgD/IgDR pathway[2][4][5][6].
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