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CXCL12 nanoparticles are a preclinical therapeutic candidate developed by the Vaccine and Immunotherapy Center (VIC) at Massachusetts General Hospital for the treatment of Type 1 Diabetes (T1D). The drug consists of the chemokine CXCL12 (C-X-C motif chemokine ligand 12, also known as stromal cell-derived factor 1 or SDF-1) formulated within or on the surface of nanoparticles. The mechanism of action involves leveraging the immunomodulatory properties of CXCL12 to protect pancreatic beta cells from autoimmune destruction. CXCL12 acts as a ligand for the CXCR4 receptor; in the context of T1D, it is designed to create an 'immunoprivileged' site by promoting the recruitment of regulatory T cells (Tregs) and potentially inducing the chemorepulsion of pathogenic effector T cells away from the islets. This approach aims to preserve endogenous beta cell function or improve the survival of transplanted islet cells without the need for chronic systemic immunosuppression.
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