| Literature DB >> 21495968 |
Yuxing Zhao1, Balasubramanian Krishnamurthy, Zia U A Mollah, Thomas W H Kay, Helen E Thomas.
Abstract
Type 1 diabetes is an autoimmune disease in which pancreatic beta cells are destroyed by autoreactive T cells. It is a common pediatric disease with increasing incidence. Islet transplantation may be a therapeutic option, however, the current limitations of this procedure mean that for most sufferers of type 1 diabetes there is no cure. The transcription factor NF-κB has been widely studied for its role in development of type 1 diabetes. Recent data have shown that NF-κB is required for activation of autoreactive T cells, and its hyperactivity in monocytes and dendritic cells results in altered cytokine secretion and antigen presentation, which ultimately contributes to the initiation of type 1 diabetes. NF-κB is also activated by a number of proinflammatory cytokines to regulate both the survival and death of beta cells. The critical role of NF-κB in type 1 diabetes renders it a promising pharmaceutical target in the intervention of this disease and further understanding of the NF-κB pathway will have an important implication on the development of novel and safe therapeutic strategies.Entities:
Mesh:
Substances:
Year: 2011 PMID: 21495968 DOI: 10.2174/187152811795564046
Source DB: PubMed Journal: Inflamm Allergy Drug Targets ISSN: 1871-5281