Title: Stem Cell-Based Therapies and Immunomodulatory Approaches in Newly Diagnosed Type 1 Diabetes
Volume: 6
Issue: 1
Author(s): Carlos Eduardo Barra Couri and Julio Cesar Voltarelli
Affiliation:
Keywords:
Diabetes mellitus, β-cell regeneration, β-cell preservation, β-cell precursors, immune intervention, stem cell, autoimmune disease, pancreatic cells., insulin, Diabetes Control, microvascular complications, metabolic syndrome, retinopathy, nephropathy, peripheral, foot ulcers, periodontal disease, hyper-glycemia appears, C-peptide plasma levels, congenital rubella syn-drome, coxsackie virus, Th1 diseases, Th2 diseases, insulitis, cytoki-nes, oxygen free radicals, Apoptosis, endoplasmic reticulum stress, chemokines, blood glucose, neogenesis, tacrolimus, prednisolone, myco-phenolate, hepatic oval cells, spleenocytes, embryonic stem cells, myocardial in-farction, immunomodula-tion, azathioprine, cyclosporine, glutamic acid descar-boxilase, cyclophosphamide, antithymocyte globulin, sitagliptin
Abstract: Type 1 diabetes mellitus is an autoimmune disease against pancreatic β cells. The autoimmune response begins months or years before the clinical presentation. At the time of hyperglycemic symptoms a small amount of β cell mass still remains. The main therapeutic option to type 1 diabetes mellitus is daily insulin injections which is shown to promote tighter glucose control and to reduce much of diabetic chronic complications. Subgroup analysis of the Diabetes Control and Complication Trial (DCCT) showed another important aspect related to long term complications of diabetes, ie, patients with initially larger residual β cell mass suffered less microvascular complications and less hypoglycemic events than those patients with small amounts of β cells at diagnosis. In face of this, β cell preservation has become another important target in the management of type 1 diabetes and its related complications. In this review, we summarize various immunomodulatory regimens ever used in humans, including stem cell-based strategies, aiming at blocking autoimmunity against pancreatic β cells and at promoting β cell preservation and/or possible β cell regeneration in recent-onset type 1 diabetes.
