[HTML][HTML] Lessons from the mouse: potential contribution of bystander lymphocyte activation by viruses to human type 1 diabetes

JA Pane, BS Coulson - Diabetologia, 2015 - Springer
JA Pane, BS Coulson
Diabetologia, 2015Springer
Viruses are considered to be potential key modulators of type 1 diabetes mellitus, with
several possible mechanisms proposed for their modes of action. Here we discuss the
evidence for virus involvement, including pancreatic infection and the induction of T cell-
mediated molecular mimicry. A particular focus of this review is the further possibility that
virus infection triggers bystander activation of pre-existing autoreactive lymphocytes. In this
scenario, the virus triggers dendritic cell maturation and proinflammatory cytokine secretion …
Abstract
Viruses are considered to be potential key modulators of type 1 diabetes mellitus, with several possible mechanisms proposed for their modes of action. Here we discuss the evidence for virus involvement, including pancreatic infection and the induction of T cell-mediated molecular mimicry. A particular focus of this review is the further possibility that virus infection triggers bystander activation of pre-existing autoreactive lymphocytes. In this scenario, the virus triggers dendritic cell maturation and proinflammatory cytokine secretion by engaging pattern recognition receptors. These proinflammatory cytokines provoke bystander autoreactive lymphocyte activation in the presence of cognate autoantigen, which leads to enhanced beta cell destruction. Importantly, this mechanism does not necessarily involve pancreatic virus infection, and its virally non-specific nature suggests that it might represent a means commonly employed by multiple viruses. The ability of viruses specifically associated with type 1 diabetes, including group B coxsackievirus, rotavirus and influenza A virus, to induce these responses is also examined. The elucidation of a mechanism shared amongst several viruses for accelerating progression to type 1 diabetes would facilitate the identification of important targets for disease intervention.
Springer