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Mapping of epitopes on the BP180 ectodomain targeted by IgA and IgG autoantibodies in patients with the lamina lucida-type of linear IgA disease

Matthias Georgi, Christian Scheckenbach, Arno Kromminga, Karin Partscht, Gerald Messer, E. B. Bröcker, D. Zillikens*

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

Linear IgA disease (LAD) is an autoimmune subepidermal blistering skin disease characterized by the linear deposition of IgA at the dermoepidermal junction. Serum from patients with LAD most commonly contains autoantibodies that are directed against the hemidesmosomal transmembrane glycoprotein BP180 (type XVII collagen). Various antigenic sites on the extracellular domain of this anchoring filament protein have been shown to be targeted by autoantibodies in different autoimmune bullous skin diseases, including bullous pemphigoid and cicatricial pemphigoid (CP). However, little is known about epitopes on BP180 recognized by autoantibodies in LAD. In this study, we used three recombinant GST fusion proteins, together roughly covering the entire BP180 ectodomain, to characterize the autoimmune response in serum from patients with LAD. Interestingly, we found both IgA and IgG reactivity to all three portions of the BP180 ectodomain. The strongest reactivity was observed with the C-terminal portion of BP180. This is also the major region recognized by autoantibodies in patients with CP. This finding correlates with the observation that there may be significant overlap of the clinical and immunopathological findings in LAD and CP.

OriginalspracheEnglisch
ZeitschriftArchives of Dermatological Research
Jahrgang293
Ausgabenummer3
Seiten (von - bis)109-114
Seitenumfang6
ISSN0340-3696
DOIs
PublikationsstatusVeröffentlicht - 2001

Fördermittel

Acknowledgements This work was supported by grant 98.073.1 from the Wilhelm Sander-Stiftung, Munich, Germany (Dr. Zil-likens). The authors are grateful to Drs. Takashi Hashimoto and Zhuxiang Nie (Department of Dermatology, Kurume University, Fukuoka, Japan) for providing the recombinant GST fusion proteins used in this study. We also thank Christine Hagel (Hamburg), and Silvana Noll and Stanislaus Reimer (Würzburg) for technical assistance. Drs. Kiehl (Hannover), Meurer (Dresden), Ogilvie (Er-langen), Sticherling (Kiel), and Stolz (Regensburg) kindly provided some of the patients’ serum samples.

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gesundheit und Wohlergehen
    SDG 3 – Gesundheit und Wohlergehen

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