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Autoantibodies to GAD65 and IA-2 in canine diabetes mellitus

Davison, L J and Weenink, S M and Christie, M R and Herrtage, M E and Catchpole, B (2008) Autoantibodies to GAD65 and IA-2 in canine diabetes mellitus. VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 126 (1-2). pp. 83-90.

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Abstract

Diabetes mellitus in dogs shares many characteristics with the human type 1 disease and virtually all diabetic dogs require insulin therapy to control hyperglycaemia. Insulin deficiency is suspected to result from immune-mediated destruction of pancreatic beta cells in some cases. Human patients Suffering from Type I A (immune-mediated) diabetes or latent autoimmune diabetes of the adult (LADA) demonstrate circulating autoantibodies against the 65 kDa isoform of glutamic acid decarboxylase (GAD65) and/or insulinoma antigen-2 (IA-2). The aims of the current study were to develop radio-immunoassays to detect serum antibodies against recombinant canine GAD65 and IA-2 and to identify diabetic dogs showing serological evidence of autoreactivity to these pancreatic beta cell antigens. Canine GAD65 and the 3' end of IA-2 (coding for amino acids 771-979 of the intracellular domain) were amplified by PCR from cDNA prepared front canine insulinoma tissue and cloned into the pCRII vector. The canine sequences were later confirmed by identifying GAD2 and PTPRN genes from the dog genome assembly. Recombinant S-35-methionine-radiolabelled canine GAD65 and IA-2 (771-979) proteins were used in radio-immunoprecipitation assays to screen sera from 30 newly diagnosed diabetic dogs and 30 control dogs. Four of 30 canine diabetic patients had significant GAD65 autoreactivity (p < 0.01) compared to controls and 3 dogs were positive for autoantibodies to IA-2 (771-979). Two diabetic dogs showed dual autoantigen reactivity. These preliminary data indicate that serological reactivity to GAD65 and IA-2 is present in a proportion of diabetic dogs and Suggests that, in some cases. canine diabetes is associated with an autoimmune response to these antigens. (C) 2008 Elsevier B.V. All rights reserved.

Item Type: Article
RVC Publication Type: Research (full) paper
WoS ID: 000261127600010
DOI: 10.1016/j.vetimm.2008.06.016
Departments: Pathology and Pathogen Biology
Depositing User: Unnamed user with email repositories@ulcc.ac.uk
Date Deposited: 12 Nov 2014 15:55
Last Modified: 30 Aug 2016 05:00
URI: http://researchonline.rvc.ac.uk/id/eprint/1421