Targeting Type 1 Diabetes Before and at the Clinical Onset of Disease

Authors: Bekris, L. M.; Kavanagh, T. J.; Lernmark, A.

Source: Endocrine, Metabolic & Immune Disorders - Drug Targets(Formerly Current Dru, Volume 6, Number 1, March 2006 , pp. 103-124(22)

Publisher: Bentham Science Publishers

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Abstract:

Autoimmune type 1 diabetes is strongly associated with a number of immune abnormalities that manifest themselves before and at the time of clinical diagnosis. The clinical onset is associated with a major loss of the pancreatic islet beta cells. Insulin treatment is the only treatment option since numerous trials with agents that suppress or modulate immune function have failed to preserve beta cell function long term. Recent studies suggest that it is possible to predict clinical onset of diabetes by combining genetic with autoantibody testing. In this review we will summarize current and future drug targets for subjects at risk for type 1 diabetes as well as for subjects with recent onset disease. We will also discuss the possible importance of initiating as well as contributing factors such as reactive oxygen species and modified autoantigens. It is speculated that drug targets of factors important to disease pathogenesis may provide safe and effective adductive treatment to preserve beta cell function in autoantibody positive subjects who are at maximum risk for disease.

Keywords: variable number tandem repeat (VNTR); CTLA-4; Viral infections; Cadmium; Oxidative Stress; antioxidant

Document Type: Research article

DOI: http://dx.doi.org/10.2174/187153006776056576

Affiliations: 1: Ake Lernmark's Laboratory, School of Medicine, University of Washington, Box 357710, Seattle, WA 206-543-0756, USA.

Publication date: 2006-03-01

More about this publication?
  • This journal is devoted to timely reviews of experimental and clinical studies in the field of endocrine, metabolic, and immune disorders. Specific emphasis is placed on humoral and cellular targets for natural, synthetic, and genetically engineered drugs that enhance or impair endocrine, metabolic, and immune parameters and functions. Topics related to the neuroendocrine-immune axis are given special emphasis in view of the growing interest in stress-related, inflammatory, autoimmune, and degenerative disorders.
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