Novel diagnostic and therapeutic approaches for autoimmune diabetes - A prime time to treat insulitis as a disease

被引:5
|
作者
Groenholm, Juha [1 ]
Lenardo, Michael J. [1 ]
机构
[1] NIAID, Mol Dev Immune Syst Sect, Immunol Lab, Clin Genom Program,NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Autoantibody; Insulitis; Type; 1; diabetes; Tolerance; RANDOMIZED CONTROLLED-TRIAL; HEAT-SHOCK-PROTEIN; BETA-CELL FUNCTION; ANTIBODY STANDARDIZATION PROGRAM; GLUTAMIC-ACID DECARBOXYLASE; RECENT-ONSET; DOUBLE-BLIND; 1ST-DEGREE RELATIVES; GENERAL-POPULATION; COXSACKIEVIRUS B1;
D O I
10.1016/j.clim.2014.11.007
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 progressive autoimmune disease with no curative treatment, making prevention critical. At the time of diagnosis, a majority of the insulin secreting beta-cells have already been destroyed. Insulitis, lymphocytic infiltration to the pancreatic islets, is believed to begin months to years before the clinical symptoms of insulin deficiency appear. Insulitis should be treated as its own disease, for it is a known precursor to autoimmune diabetes. Because it is difficult to detect insulitic cellular infiltrates noninvasively, considerable interest has been focused on the levels of islet autoantibodies in blood as measurable diagnostic markers for islet autoimmunity. The traditional islet autoantibody detection assays have many limitations. New electrochemiluminescence-based autoantibody detection assays have the potential to overcome these challenges and they offer promising, cost-effective screening tools in identifying high-risk individuals for trials of preventive interventions. Here, we outline diagnostic and therapeutic strategies to overcome pancreatic beta-cell destroying insulitis. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:109 / 118
页数:10
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