Abstract
Two fundamental aspects for precisely predicting the risk of developing type 1 diabetes by islet autoantibodies are assay sensitivity and disease specificity. We have recently developed electrochemiluminescent (ECL) insulin autoantibody (IAA) and GAD65 autoantibody (GADA) assays. ECL assays are sensitive, able to identify the initiation of islet autoimmunity earlier in life among high-risk young children before clinical onset of diabetes and are more disease specific because they are able to discriminate high-affinity, high-risk diabetes specific islet autoantibodies from low-affinity, low-risk autoantibodies.
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Acknowledgement
This study was supported by NIH grant DK32083, Diabetes Autoimmunity Study in the Young Grant DK32493, the Immune Tolerance Network AI15416, the Juvenile Diabetes Research Foundation Grant 11-2005-15, DERC Clinical Core DK57516. We thank Dr. Tom Thomas of Vanderbilt for the gift of an insulin monoclonal antibody. We thank Eli Lilly Company for supplying proinsulin and thank MSD Company for helpful discussions during assay development.
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Yu, L. (2015). Islet Autoantibody Detection by Electrochemiluminescence (ECL) Assay. In: Gillespie, K. (eds) Type-1 Diabetes. Methods in Molecular Biology, vol 1433. Humana Press, New York, NY. https://doi.org/10.1007/7651_2015_296
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DOI: https://doi.org/10.1007/7651_2015_296
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Publisher Name: Humana Press, New York, NY
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