Islet tyrosine phosphatase 2 (IA-2) is one of the major autoantigens in type 1 diabetes. The aim of this work was to evaluate which IA-2 construct(s) among those usually employed has the highest sensitivity and specificity for detecting IA-2 autoantibodies in autoimmune diabetes and whether the combination of different IA-2 constructs into a single assay allows the detection of immunoreactivities otherwise not detectable by a single construct. For this purpose, we tested the single immunoreactivities of IA-2(FL)(aa 1-979), IA-2(BDC)(aa 256-556:630979), IA-2(IC)(aa 605-979), IA-2(aa 256-760), IA-2(aa 761-928), and of 7 combinations of these fragments in the sera of 203 newly diagnosed type 1 diabetic patient (DM: 109 males,94 females, mean age 12.9 +/- 7.5 years) and 43 prediabetic subject (PDM: 20 males, 23 females, mean age 10.3 +/- 6.0 years) sera. IA-2(IC) was the single construct that showed the highest sensitivity and specificity both in DM and PDM subjects, however, all of the other IA-2 constructs investigated detected additional immunoreactivities with respect to it. The combined use into the same assay of IA-2(IC), IA-2(FL), and IA-2((256-760)) constructs allowed detection of IA-2 Abs in additional 13.3% DM and 30.4% PDM subjects compared to the single IA-2(IC) construct, suggesting this methodology as a new, highly sensitive approach to the study of IA-2 autoimmunity in type 1 diabetes. (c) 2005 Elsevier Inc. All rights reserved.

IA-2 combined epitope assay: a new, highly sensitive approach to evaluate IA-2 humoral autoimmunity in type 1 diabetes / Tiberti, Claudio; Verrienti, Antonella; Fiore, Benedetta; Yu, Liping; Eisenbarth, George S; Dotta, Francesco; Di Mario, Umberto. - In: CLINICAL IMMUNOLOGY. - ISSN 1521-6616. - 115:3(2005), pp. 260-267. [10.1016/j.clim.2005.01.015]

IA-2 combined epitope assay: a new, highly sensitive approach to evaluate IA-2 humoral autoimmunity in type 1 diabetes

Tiberti, Claudio
;
Verrienti, Antonella;Fiore, Benedetta;Dotta, Francesco;Di Mario, Umberto
2005

Abstract

Islet tyrosine phosphatase 2 (IA-2) is one of the major autoantigens in type 1 diabetes. The aim of this work was to evaluate which IA-2 construct(s) among those usually employed has the highest sensitivity and specificity for detecting IA-2 autoantibodies in autoimmune diabetes and whether the combination of different IA-2 constructs into a single assay allows the detection of immunoreactivities otherwise not detectable by a single construct. For this purpose, we tested the single immunoreactivities of IA-2(FL)(aa 1-979), IA-2(BDC)(aa 256-556:630979), IA-2(IC)(aa 605-979), IA-2(aa 256-760), IA-2(aa 761-928), and of 7 combinations of these fragments in the sera of 203 newly diagnosed type 1 diabetic patient (DM: 109 males,94 females, mean age 12.9 +/- 7.5 years) and 43 prediabetic subject (PDM: 20 males, 23 females, mean age 10.3 +/- 6.0 years) sera. IA-2(IC) was the single construct that showed the highest sensitivity and specificity both in DM and PDM subjects, however, all of the other IA-2 constructs investigated detected additional immunoreactivities with respect to it. The combined use into the same assay of IA-2(IC), IA-2(FL), and IA-2((256-760)) constructs allowed detection of IA-2 Abs in additional 13.3% DM and 30.4% PDM subjects compared to the single IA-2(IC) construct, suggesting this methodology as a new, highly sensitive approach to the study of IA-2 autoimmunity in type 1 diabetes. (c) 2005 Elsevier Inc. All rights reserved.
2005
type 1 diabetes; autoinimunity; combined epitopes; islet tyrosine phosphatase 2 (IA-2)
01 Pubblicazione su rivista::01a Articolo in rivista
IA-2 combined epitope assay: a new, highly sensitive approach to evaluate IA-2 humoral autoimmunity in type 1 diabetes / Tiberti, Claudio; Verrienti, Antonella; Fiore, Benedetta; Yu, Liping; Eisenbarth, George S; Dotta, Francesco; Di Mario, Umberto. - In: CLINICAL IMMUNOLOGY. - ISSN 1521-6616. - 115:3(2005), pp. 260-267. [10.1016/j.clim.2005.01.015]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1681568
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