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Non-antigenic and antigenic interventions in type 1 diabetes.


ABSTRACT: Type 1 diabetes (T1D) results from autoimmune destruction of the pancreatic ?-cells. Current T1D therapies are exclusively focused on regulating glycemia rather than the underlying immune response. A handful of trials have sought to alter the clinical course of T1D using various broad immune-suppressors, e.g., cyclosporine A and azathioprine.(1-3) The effect on ?-cell preservation was significant, however, these therapies were associated with unacceptable side-effects. In contrast, more recent immunomodulators, such as anti-CD3 and antigenic therapies such as DiaPep277, provide a more targeted immunomodulation and have been generally well-tolerated and safe; however, as a monotherapy there appear to be limitations in terms of therapeutic benefit. Therefore, we argue that this new generation of immune-modifying agents will likely work best as part of a combination therapy. This review will summarize current immune-modulating therapies under investigation and discuss how to move the field of immunotherapy in T1D forward.

SUBMITTER: Ryden AK 

PROVIDER: S-EPMC4896560 | biostudies-literature | 2014

REPOSITORIES: biostudies-literature

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Non-antigenic and antigenic interventions in type 1 diabetes.

Rydén Anna K E AK   Wesley Johnna D JD   Coppieters Ken T KT   Von Herrath Matthias G MG  

Human vaccines & immunotherapeutics 20131028 4


Type 1 diabetes (T1D) results from autoimmune destruction of the pancreatic β-cells. Current T1D therapies are exclusively focused on regulating glycemia rather than the underlying immune response. A handful of trials have sought to alter the clinical course of T1D using various broad immune-suppressors, e.g., cyclosporine A and azathioprine.(1-3) The effect on β-cell preservation was significant, however, these therapies were associated with unacceptable side-effects. In contrast, more recent i  ...[more]

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