surface plasmon resonance reveals a different pattern of proinsulin autoantibodies concentration and affinity in diabetic patients表面等离子体共振揭示了一个不同的模式在糖尿病患者胰岛素原的自体抗体浓度和亲和力.pdfVIP
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surface plasmon resonance reveals a different pattern of proinsulin autoantibodies concentration and affinity in diabetic patients表面等离子体共振揭示了一个不同的模式在糖尿病患者胰岛素原的自体抗体浓度和亲和力
Surface Plasmon Resonance Reveals a Different Pattern
of Proinsulin Autoantibodies Concentration and Affinity
in Diabetic Patients
´
Aldana Trabucchi, Luciano L. Guerra, Natalia I. Faccinetti, Ruben F. Iacono, Edgardo Poskus,
Silvina N. Valdez*
School of Pharmacy and Biochemistry, University of Buenos Aires (UBA), and Humoral Immunity Institute Prof. Ricardo A. Margni (IDEHU), National Research Council
(CONICET)-UBA, Buenos Aires, Argentina
Abstract
Type 1 diabetes mellitus (DM) is characterized by autoimmune aggression against pancreatic beta cells resulting in absolute
deficiency of insulin secretion. The first detectable sign of emerging autoimmunity during the preclinical asymptomatic
period is the appearance of diabetes-related autoantibodies. In children at risk for type 1 DM, high-affinity Insulin
autoantibodies reactive to proinsulin, are associated with diabetes risk. Autoantibodies are usually measured by radioligand
binding assay (RBA) that provides quasi-quantitative values reflecting potency (product between concentration and affinity)
of specific autoantibodies. Aiming to improve the characterization of the specific humoral immune response, we selected
surface plasmon resonance (SPR) as an alternative method to measure proinsulin autoantibodies (PAA). This novel
technology has allowed real time detection of antibodies interaction and kinetic analysis. Herein, we have employed SPR to
characterize the PAA present in sera from 28 childhood-onset (mean age 8.31 64.20) and 23 adult-onset diabetic patients
($65 years old, BMI,30) in terms of concentration and affinity. When evaluating comparatively samples from both groups,
childhood-onset diabetic patients presented lowe
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