DiaPep277® and immune intervention for treatment of type 1 diabetes

被引:12
|
作者
Schloot, Nanette C. [1 ]
Cohen, Lrun R. [2 ]
机构
[1] Univ Dusseldorf, German Diabet Ctr, Leibniz Ctr Diabet, Inst Clin Diabetol, D-40225 Dusseldorf, Germany
[2] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
关键词
Type; 1; diabetes; C-peptide; Immunotherapy; T cells; BETA-CELL FUNCTION; HEAT-SHOCK-PROTEIN; RANDOMIZED CONTROLLED-TRIAL; PHASE-II TRIAL; DOUBLE-BLIND; C-PEPTIDE; T-CELLS; HLA GENOTYPES; NOD MICE; ONSET;
D O I
10.1016/j.clim.2013.09.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Type 1 diabetes is a chronic immune-mediated disease resulting in destruction of insulin-producing beta-cells. Several studies have been performed aiming to halt disease progression after diagnosis; to reduce the increased diabetes risk in islet-autoantibody positive subjects; and to prevent the onset of beta-cell autoimmunity in subjects genetically at risk but without autoantibodies. Whereas secondary prevention trials failed, trials in newly diagnosed patients have shown partial success in preserving C-peptide. These studies target T-cells and inflammation and make use of antigen-specific immune modulation or stem cell approaches. However, thus far no immune-based therapeutic regimen has cured type 1 diabetes after its clinical onset or has stabilized the decline of C-peptide to achieve the status of an approved drug. This review summarizes immune intervention trials and the current knowledge of DiaPep277(R) peptide as a form of immune intervention in type 1 diabetes. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:307 / 316
页数:10
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