Coxsackie B4 virus infection of β cells and natural killer cell insulitis in recent-onset type 1 diabetic patients

Francesco Dotta(University of Siena), Stefano Censini(Toscana Life Sciences), Astrid G. S. van Halteren(Leiden University Medical Center), Lorella Marselli(University of Pisa), Matilde Masini(University of Pisa), Sabrina Dionisi(University of Siena), Franco Mosca(University of Pisa), Ugo Boggi(University of Pisa), Andrea Onetti Muda(Sapienza University of Rome), Stefano Del Prato(University of Pisa), John F. Elliott(University of Alberta), Antonello Covacci(Toscana Life Sciences), Rino Rappuoli(Toscana Life Sciences), Bart O. Roep(Leiden University Medical Center), Piero Marchetti(University of Pisa)
Proceedings of the National Academy of Sciences
March 14, 2007
Cited by 566

Abstract

Type 1 diabetes is characterized by T cell-mediated autoimmune destruction of pancreatic beta cells. Several studies have suggested an association between Coxsackie enterovirus seroconversion and onset of disease. However, a direct link between beta cell viral infection and islet inflammation has not been established. We analyzed pancreatic tissue from six type 1 diabetic and 26 control organ donors. Immunohistochemical, electron microscopy, whole-genome ex vivo nucleotide sequencing, cell culture, and immunological studies demonstrated Coxsackie B4 enterovirus in specimens from three of the six diabetic patients. Infection was specific of beta cells, which showed nondestructive islet inflammation mediated mainly by natural killer cells. Islets from enterovirus-positive samples displayed reduced insulin secretion in response to glucose and other secretagogues. In addition, virus extracted from positive islets was able to infect beta cells from human islets of nondiabetic donors, causing viral inclusions and signs of pyknosis. None of the control organ donors showed signs of viral infection. These studies provide direct evidence that enterovirus can infect beta cells in patients with type 1 diabetes and that infection is associated with inflammation and functional impairment.


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