Literature DB >> 22861364

The immunobiology of apotransferrin in type 1 diabetes.

K Mangano1, P Fagone, M Di Mauro, E Ascione, V Maiello, T Milicic, A Jotic, N M Lalic, T Saksida, I Stojanovic, C Selmi, C Farina, S Stosic-Grujicic, P Meroni, F Nicoletti.   

Abstract

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.
© 2012 The Authors. Clinical and Experimental Immunology © 2012 British Society for Immunology.

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Year:  2012        PMID: 22861364      PMCID: PMC3445001          DOI: 10.1111/j.1365-2249.2012.04619.x

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


  32 in total

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