High-throughput radioassays for autoantibodies to recombinant autoantigens

被引:16
作者
Kawasaki, E
Eisenbarth, GS
机构
[1] Univ Colorado, Hlth Sci Ctr, Barbara Davis Ctr Childhood Diabet, Denver, CO 80262 USA
[2] Nagasaki Univ, Sch Med, Dept Internal Med 1, Nagasaki 8528501, Japan
关键词
autoimmunity; autoantibody; autoantigen; radioassay; prediction; epitope; review;
D O I
10.2741/kawasaki
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Advances in immunology, biochemistry, and molecular biology have combined to allow the development of a large series of autoantibody assays utilizing recombinantly produced autoantigens. Labeled target proteins can be readily produced by in vitro transcription and translation of relevant cloned cDNA. The assays are carried out in the fluid phase and for most assays are more specific and sensitive than ELISA based assays. For some antigens (e.g. insulin) though ELISA assays detect antibodies following immunization, workshops indicate they are almost worthless for the diagnosis and prediction of type 1A diabetes. This new generation of radioassays is usually carried out in 96-well microtiter filtration plates that allow high throughput. Given such assays, individuals at high risk for type 1A diabetes, celiac disease, and Addison's disease can now be readily identified.
引用
收藏
页码:E181 / E190
页数:10
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