Gluten sensitivity typically presents as celiac disease, a common chronic small intestinal disorder. However, in certain individuals it is associated with dermatitis herpetiformis, a blistering skin disease characterized by granular IgA deposits in the papillary dermis. While tissue transglutaminase has been implicated as the major autoantigen of gluten sensitive disease, there has been no explanation as to why this condition appears in two distinct forms. Here we show that while sera from patients with either form of gluten sensitive disease react both with tissue transglutaminase and the related enzyme epidermal (type 3) transglutaminase, antibodies in patients having dermatitis herpetiformis show a markedly higher avidity for epidermal transglutaminase. Further, these patients have an antibody population specific for this enzyme. We also show that the IgA precipitates in the papillary dermis of patients with dermatitis herpetiformis, the defining signs of the disease, contain epidermal transglutaminase, but not tissue transglutaminase or keratinocyte transglutaminase. These findings demonstrate that epidermal transglutaminase, rather than tissue transglutaminase, is the dominant autoantigen in dermatitis herpetiformis and explain why skin symptoms appear in a proportion of patients having gluten sensitive disease.
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18 March 2002
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March 18 2002
Epidermal Transglutaminase (TGase 3) Is the Autoantigen of Dermatitis Herpetiformis
Miklós Sárdy,
Miklós Sárdy
1Department of Dermato-Venereology, Semmelweis University, H-1085 Budapest, Hungary
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Sarolta Kárpáti,
Sarolta Kárpáti
1Department of Dermato-Venereology, Semmelweis University, H-1085 Budapest, Hungary
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Barbara Merkl,
Barbara Merkl
2Institute for Biochemistry II, Medical Faculty, University of Cologne, D-50931 Cologne, Germany
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Mats Paulsson,
Mats Paulsson
2Institute for Biochemistry II, Medical Faculty, University of Cologne, D-50931 Cologne, Germany
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Neil Smyth
Neil Smyth
2Institute for Biochemistry II, Medical Faculty, University of Cologne, D-50931 Cologne, Germany
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Miklós Sárdy
1Department of Dermato-Venereology, Semmelweis University, H-1085 Budapest, Hungary
Sarolta Kárpáti
1Department of Dermato-Venereology, Semmelweis University, H-1085 Budapest, Hungary
Barbara Merkl
2Institute for Biochemistry II, Medical Faculty, University of Cologne, D-50931 Cologne, Germany
Mats Paulsson
2Institute for Biochemistry II, Medical Faculty, University of Cologne, D-50931 Cologne, Germany
Neil Smyth
2Institute for Biochemistry II, Medical Faculty, University of Cologne, D-50931 Cologne, Germany
Address correspondence to Dr. M. Sárdy, Dept. of Dermato-Venereology, Semmelweis University, H-1085 Budapest, Mária u. 41, Hungary. Phone: 36-1-266-0465/5718; Fax: 36-1-267-6974; E-mail: [email protected]
*
Abbreviations used in this paper: AU, arbitrary unit(s); CD, celiac disease; CI, confidence interval; DH, dermatitis herpetiformis; EMA, endomysium Ab; GSD, gluten sensitive disease; GSE, gluten sensitive enteropathy; TG, transglutaminase; TGc, tissue (cellular, type 2) transglutaminase; TGe, epidermal (type 3) transglutaminase; TGk, keratinocyte (type 1) transglutaminase; TGx, type 5 transglutaminase.
Received:
July 26 2001
Revision Received:
January 08 2002
Accepted:
February 07 2002
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2002
J Exp Med (2002) 195 (6): 747–757.
Article history
Received:
July 26 2001
Revision Received:
January 08 2002
Accepted:
February 07 2002
Citation
Miklós Sárdy, Sarolta Kárpáti, Barbara Merkl, Mats Paulsson, Neil Smyth; Epidermal Transglutaminase (TGase 3) Is the Autoantigen of Dermatitis Herpetiformis . J Exp Med 18 March 2002; 195 (6): 747–757. doi: https://doi.org/10.1084/jem.20011299
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