Literature DB >> 16544364

Anti-CD38 autoantibodies in type? diabetes.

Roberto Mallone1, Paolo Cavallo Perin.   

Abstract

Human diabetes mellitus comprises two main clinical entities: type 1 and type 2 diabetes. While type 1 diabetes is autoimmune in origin, type 2 diabetes is due to a decreased sensitivity to insulin action (so-called insulin resistance) associated with impaired beta cell function. However, it is becoming increasingly clear that there is a certain overlap between these two diseases. While some degree of insulin resistance is present in type 1 diabetic patients, markers of beta cell autoimmunity (either primary or secondary) can frequently be detected in type 2 diabetic subjects. In this scenario, anti-CD38 autoantibodies (aAbs) have been described in both type 1 and type 2 diabetic patients. Contrary to the other known islet aAbs, anti-CD38 autoantibodies are more prevalent in long-standing than in new-onset type 1 diabetes, and more prevalent in type 2 than in type 1 diabetes. Moreover, anti-CD38 aAbs are endowed with unique stimulatory properties on Ca(2+) mobilization and insulin secretion. These observations suggest that autoimmunity may be both the cause and consequence of beta cell dysfunction, in either case imposing a further toll for the control of glucose homeostasis. Copyright (c) 2006 John Wiley & Sons, Ltd.

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Year:  2006        PMID: 16544364      PMCID: PMC2763400          DOI: 10.1002/dmrr.626

Source DB:  PubMed          Journal:  Diabetes Metab Res Rev        ISSN: 1520-7552            Impact factor:   4.876


  83 in total

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Journal:  Gene       Date:  1997-02-28       Impact factor: 3.688

9.  Post-translational modification of CD38 protein into a high molecular weight form alters its catalytic properties.

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10.  Secretion of IFN-gamma, IL-6, granulocyte-macrophage colony-stimulating factor and IL-10 cytokines after activation of human purified T lymphocytes upon CD38 ligation.

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Journal:  Cell Immunol       Date:  1996-11-01       Impact factor: 4.868

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  4 in total

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