| Literature DB >> 20920845 |
Peter Achenbach1, Liang-Hao Guo, Claudia Gick, Kerstin Adler, Stephanie Krause, Ezio Bonifacio, Peter G Colman, Anette-G Ziegler.
Abstract
Insulin autoantibodies (IAA) precede type 1 diabetes, but not all IAA-positive children develop other islet autoantibodies and disease. Diabetes risk can be stratified by laborious IAA affinity measurement using competition with multiple ligand concentrations. Here, we identify a single competitor concentration that discriminates low- and high-affinity IAA. Discrimination was achieved among 122 IAA-positive sera using 7.0 nM competitor which is 54-fold that of the assay radioligand concentration. Relative-binding <60% at this competitor concentration identified all 85 sera with affinities ≥1.0×10⁸ L/mol and none with lower affinities (P<0.0001), and 45 (96%) of 47 multiple islet autoantibody-positive sera (P<0.0001). IAA competition was further tested in a second set of 119 IAA-positive sera. Of these, 99 fulfilled high-affinity competition criteria of <60% relative-binding at 7.0 nM competitor including 89 (94%) of 95 sera with multiple islet autoantibodies (P<0.0001). Thus, increased IAA specificity can be achieved with simple modification to existing assays.Entities:
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Year: 2010 PMID: 20920845 DOI: 10.1016/j.clim.2010.09.002
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969