GAD65 Autoantibodies in Kleine-Levin Syndrome

2014 ◽  
Vol 26 (2) ◽  
pp. E49-E51 ◽  
Author(s):  
Ujjwal K. Rout ◽  
Meeta Shah Michener ◽  
Dirk M. Dhossche
Keyword(s):  
Diabetologia ◽  
1996 ◽  
Vol 39 (9) ◽  
pp. 1091-1098 ◽  
Author(s):  
A. Falorni ◽  
M. Ackefors ◽  
C. Carlberg ◽  
T. Daniels ◽  
B. Persson ◽  
...  

2006 ◽  
Vol 119 ◽  
pp. S169 ◽  
Author(s):  
Barbro Holm ◽  
Eero Lindholm ◽  
Kristian Lynch ◽  
Ekaterina Bakhatadze ◽  
Jeanette Arvastsson ◽  
...  

2012 ◽  
Vol 21 (3) ◽  
pp. 141-147 ◽  
Author(s):  
Ujjwal K. Rout ◽  
Nils K. Mungan ◽  
Dirk M. Dhossche

PLoS ONE ◽  
2010 ◽  
Vol 5 (5) ◽  
pp. e10838 ◽  
Author(s):  
Marta Rizzi ◽  
Rolf Knoth ◽  
Christiane S. Hampe ◽  
Peter Lorenz ◽  
Marie-Lise Gougeon ◽  
...  

2005 ◽  
Vol 153 (6) ◽  
pp. 901-906 ◽  
Author(s):  
Matti S Ronkainen ◽  
Taina Härkönen ◽  
Jaakko Perheentupa ◽  
Mikael Knip

Objective: A humoral autoimmune response to glutamic acid decarboxylase (GAD65) is common both in patients with type 1 diabetes and in those with the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) syndrome, while overt type 1 diabetes is relatively rarely diagnosed in APECED patients. The aim of this study was to assess whether this difference in the incidence of type 1 diabetes is associated with variability in the humoral immune response to GAD65, one of the major autoantigens in type 1 diabetes. Methods: Epitope- and isotype-specific GAD65 autoantibodies were analysed in 20 patients with APECED and 20 patients with newly diagnosed type 1 diabetes alone by radiobinding assays. Results: GAD65 autoantibodies targeted the middle and carboxy-terminal regions of GAD65 and occasionally the amino-terminal region in the APECED patients and comprised mainly the IgG1 subclass and less frequently the IgG2 and IgG4 subclasses. The profile of epitope- and isotype-specific GAD65 autoantibodies was similar in type 1 diabetes and APECED, except that IgG2 subclass antibodies were observed more often and at higher levels in the patients with type 1 diabetes alone (P < 0.05). None of the measured parameters separated APECED patients with type 1 diabetes from those without type 1 diabetes. Conclusion: APECED-associated humoral autoimmunity to GAD65 does not differ markedly from that observed in type 1 diabetes; only IgG2-GAD65 antibodies may be more closely associated with the latter entity.


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