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

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 autoantige...

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Autores principales: Landegren, Nils, Ishii, Norito, Aranda-Guillén, Maribel, Gunnarsson, Hörður Ingi, Sardh, Fabian, Hallgren, Åsa, Ståhle, Mona, Hagforsen, Eva, Bradley, Maria, Edqvist, Per-Henrik D., Pontén, Fredrik, Mäkitie, Outi, Eidsmo, Liv, Norlén, Lars, Achour, Adnane, Dahlbom, Ingrid, Korponay-Szabó, Ilma, Agardh, Daniel, Alimohammadi, Mohammad, Eriksson, Daniel, Hashimoto, Takashi, Kämpe, Olle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8713791/
https://www.ncbi.nlm.nih.gov/pubmed/34911754
http://dx.doi.org/10.1073/pnas.2100687118
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author Landegren, Nils
Ishii, Norito
Aranda-Guillén, Maribel
Gunnarsson, Hörður Ingi
Sardh, Fabian
Hallgren, Åsa
Ståhle, Mona
Hagforsen, Eva
Bradley, Maria
Edqvist, Per-Henrik D.
Pontén, Fredrik
Mäkitie, Outi
Eidsmo, Liv
Norlén, Lars
Achour, Adnane
Dahlbom, Ingrid
Korponay-Szabó, Ilma
Agardh, Daniel
Alimohammadi, Mohammad
Eriksson, Daniel
Hashimoto, Takashi
Kämpe, Olle
author_facet Landegren, Nils
Ishii, Norito
Aranda-Guillén, Maribel
Gunnarsson, Hörður Ingi
Sardh, Fabian
Hallgren, Åsa
Ståhle, Mona
Hagforsen, Eva
Bradley, Maria
Edqvist, Per-Henrik D.
Pontén, Fredrik
Mäkitie, Outi
Eidsmo, Liv
Norlén, Lars
Achour, Adnane
Dahlbom, Ingrid
Korponay-Szabó, Ilma
Agardh, Daniel
Alimohammadi, Mohammad
Eriksson, Daniel
Hashimoto, Takashi
Kämpe, Olle
author_sort Landegren, Nils
collection PubMed
description 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.
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spelling pubmed-87137912022-01-21 A gene-centric approach to biomarker discovery identifies transglutaminase 1 as an epidermal autoantigen Landegren, Nils Ishii, Norito Aranda-Guillén, Maribel Gunnarsson, Hörður Ingi Sardh, Fabian Hallgren, Åsa Ståhle, Mona Hagforsen, Eva Bradley, Maria Edqvist, Per-Henrik D. Pontén, Fredrik Mäkitie, Outi Eidsmo, Liv Norlén, Lars Achour, Adnane Dahlbom, Ingrid Korponay-Szabó, Ilma Agardh, Daniel Alimohammadi, Mohammad Eriksson, Daniel Hashimoto, Takashi Kämpe, Olle Proc Natl Acad Sci U S A Biological Sciences 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. National Academy of Sciences 2021-12-15 2021-12-21 /pmc/articles/PMC8713791/ /pubmed/34911754 http://dx.doi.org/10.1073/pnas.2100687118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Landegren, Nils
Ishii, Norito
Aranda-Guillén, Maribel
Gunnarsson, Hörður Ingi
Sardh, Fabian
Hallgren, Åsa
Ståhle, Mona
Hagforsen, Eva
Bradley, Maria
Edqvist, Per-Henrik D.
Pontén, Fredrik
Mäkitie, Outi
Eidsmo, Liv
Norlén, Lars
Achour, Adnane
Dahlbom, Ingrid
Korponay-Szabó, Ilma
Agardh, Daniel
Alimohammadi, Mohammad
Eriksson, Daniel
Hashimoto, Takashi
Kämpe, Olle
A gene-centric approach to biomarker discovery identifies transglutaminase 1 as an epidermal autoantigen
title A gene-centric approach to biomarker discovery identifies transglutaminase 1 as an epidermal autoantigen
title_full A gene-centric approach to biomarker discovery identifies transglutaminase 1 as an epidermal autoantigen
title_fullStr A gene-centric approach to biomarker discovery identifies transglutaminase 1 as an epidermal autoantigen
title_full_unstemmed A gene-centric approach to biomarker discovery identifies transglutaminase 1 as an epidermal autoantigen
title_short A gene-centric approach to biomarker discovery identifies transglutaminase 1 as an epidermal autoantigen
title_sort gene-centric approach to biomarker discovery identifies transglutaminase 1 as an epidermal autoantigen
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8713791/
https://www.ncbi.nlm.nih.gov/pubmed/34911754
http://dx.doi.org/10.1073/pnas.2100687118
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