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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.
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页码:307 / 316
页数:10
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