The immunobiology of apotransferrin in type 1 diabetes

Author:

Mangano K1,Fagone P1,Di Mauro M1,Ascione E2,Maiello V2,Milicic T3,Jotic A3,Lalic N M3,Saksida T4,Stojanovic I4,Selmi C56,Farina C2,Stosic-Grujicic S4,Meroni P7,Nicoletti F1

Affiliation:

1. Department of Bio-medical Sciences, University of Catania, Catania

2. Kedrion Research, S. Antimo, Napoli

3. Clinic for Endocrinology, Diabetes and Metabolic Diseases, Clinical Center of Serbia, Faculty of Medicine, University of Belgrade

4. Department of Immunology, Institute for Biological Research ‘Sinisa Stankovic’, Belgrade University, Belgrade, Serbia

5. Autoimmunity and Metabolism Unit, IRCCS Istituto Clinico Humanitas, Rozzano, Milano

6. Department of Translational Medicine

7. Department of Internal Medicine, University of Milan, Milan, Italy

Abstract

Summary The transferrin (Tf) family of iron binding proteins includes important endogenous modulators of the immune function that may modulate autoimmune diseases. To define more clearly the role of apotransferrin (apoTf) in type 1 diabetes we determined the impact of this protein on type 1 diabetes as investigated in islet cells, animal models and patient sera. First, we demonstrated that recombinant apoTf counteracts the cytokine-induced death of murine pancreatic islet cells. Secondly, human apoTf administration favourably influences the course of type 1 diabetes in animal models, resulting in protection against disease development that was associated with reduction of insulitis and reduced levels of proinflammatory cytokines. Finally, we confirmed that patients with newly diagnosed type 1 diabetes manifest significantly lower apoTf serum levels compared to healthy controls and patients with long-lasting disease. In conclusion, our data suggest the apoTf pivotal role in the perpetuation of type 1 diabetes pathology.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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