A gene-centric approach to biomarker discovery identifies transglutaminase 1 as an epidermal autoantigen

Author:

Landegren NilsORCID,Ishii NoritoORCID,Aranda-Guillén MaribelORCID,Gunnarsson Hörður Ingi,Sardh Fabian,Hallgren Åsa,Ståhle MonaORCID,Hagforsen Eva,Bradley MariaORCID,Edqvist Per-Henrik D.ORCID,Pontén FredrikORCID,Mäkitie OutiORCID,Eidsmo Liv,Norlén Lars,Achour AdnaneORCID,Dahlbom IngridORCID,Korponay-Szabó IlmaORCID,Agardh DanielORCID,Alimohammadi MohammadORCID,Eriksson DanielORCID,Hashimoto TakashiORCID,Kämpe OlleORCID

Abstract

Autoantigen discovery is a critical challenge for the understanding and diagnosis of autoimmune diseases. While autoantibody markers in current clinical use have been identified through studies focused on individual disorders, we postulated that a reverse approach starting with a putative autoantigen to explore multiple disorders might hold promise. We here targeted the epidermal protein transglutaminase 1 (TGM1) as a member of a protein family prone to autoimmune attack. By screening sera from patients with various acquired skin disorders, we identified seropositive subjects with the blistering mucocutaneous disease paraneoplastic pemphigus. Validation in further subjects confirmed TGM1 autoantibodies as a 55% sensitive and 100% specific marker for paraneoplastic pemphigus. This gene-centric approach leverages the wealth of data available for human genes and may prove generally applicable for biomarker discovery in autoimmune diseases.

Funder

The Swedish Research Council

Knut och Alice Wallenbergs Stiftelse

the Swedish Society for Medical Research

the Göran Gustafsson Foundation

Novo Nordisk UK Research Foundation

the AMED

the Hungarian Research Fund

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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