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ILF2 and ILF3 are autoantigens in canine systemic autoimmune disease

Dogs can spontaneously develop complex systemic autoimmune disorders, with similarities to human autoimmune disease. Autoantibodies directed at self-antigens are a key feature of these autoimmune diseases. Here we report the identification of interleukin enhancer-binding factors 2 and 3 (ILF2 and IL...

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Autores principales: Bremer, Hanna D., Landegren, Nils, Sjöberg, Ronald, Hallgren, Åsa, Renneker, Stefanie, Lattwein, Erik, Leonard, Dag, Eloranta, Maija-Leena, Rönnblom, Lars, Nordmark, Gunnel, Nilsson, Peter, Andersson, Göran, Lilliehöök, Inger, Lindblad-Toh, Kerstin, Kämpe, Olle, Hansson-Hamlin, Helene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859008/
https://www.ncbi.nlm.nih.gov/pubmed/29556082
http://dx.doi.org/10.1038/s41598-018-23034-w
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author Bremer, Hanna D.
Landegren, Nils
Sjöberg, Ronald
Hallgren, Åsa
Renneker, Stefanie
Lattwein, Erik
Leonard, Dag
Eloranta, Maija-Leena
Rönnblom, Lars
Nordmark, Gunnel
Nilsson, Peter
Andersson, Göran
Lilliehöök, Inger
Lindblad-Toh, Kerstin
Kämpe, Olle
Hansson-Hamlin, Helene
author_facet Bremer, Hanna D.
Landegren, Nils
Sjöberg, Ronald
Hallgren, Åsa
Renneker, Stefanie
Lattwein, Erik
Leonard, Dag
Eloranta, Maija-Leena
Rönnblom, Lars
Nordmark, Gunnel
Nilsson, Peter
Andersson, Göran
Lilliehöök, Inger
Lindblad-Toh, Kerstin
Kämpe, Olle
Hansson-Hamlin, Helene
author_sort Bremer, Hanna D.
collection PubMed
description Dogs can spontaneously develop complex systemic autoimmune disorders, with similarities to human autoimmune disease. Autoantibodies directed at self-antigens are a key feature of these autoimmune diseases. Here we report the identification of interleukin enhancer-binding factors 2 and 3 (ILF2 and ILF3) as autoantigens in canine immune-mediated rheumatic disease. The ILF2 autoantibodies were discovered in a small, selected canine cohort through the use of human protein arrays; a method not previously described in dogs. Subsequently, ILF3 autoantibodies were also identified in the same cohort. The results were validated with an independent method in a larger cohort of dogs. ILF2 and ILF3 autoantibodies were found exclusively, and at a high frequency, in dogs that showed a speckled pattern of antinuclear antibodies on immunofluorescence. ILF2 and ILF3 autoantibodies were also found at low frequency in human patients with SLE and Sjögren’s syndrome. These autoantibodies have the potential to be used as diagnostic biomarkers for canine, and possibly also human, autoimmune disease.
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spelling pubmed-58590082018-03-20 ILF2 and ILF3 are autoantigens in canine systemic autoimmune disease Bremer, Hanna D. Landegren, Nils Sjöberg, Ronald Hallgren, Åsa Renneker, Stefanie Lattwein, Erik Leonard, Dag Eloranta, Maija-Leena Rönnblom, Lars Nordmark, Gunnel Nilsson, Peter Andersson, Göran Lilliehöök, Inger Lindblad-Toh, Kerstin Kämpe, Olle Hansson-Hamlin, Helene Sci Rep Article Dogs can spontaneously develop complex systemic autoimmune disorders, with similarities to human autoimmune disease. Autoantibodies directed at self-antigens are a key feature of these autoimmune diseases. Here we report the identification of interleukin enhancer-binding factors 2 and 3 (ILF2 and ILF3) as autoantigens in canine immune-mediated rheumatic disease. The ILF2 autoantibodies were discovered in a small, selected canine cohort through the use of human protein arrays; a method not previously described in dogs. Subsequently, ILF3 autoantibodies were also identified in the same cohort. The results were validated with an independent method in a larger cohort of dogs. ILF2 and ILF3 autoantibodies were found exclusively, and at a high frequency, in dogs that showed a speckled pattern of antinuclear antibodies on immunofluorescence. ILF2 and ILF3 autoantibodies were also found at low frequency in human patients with SLE and Sjögren’s syndrome. These autoantibodies have the potential to be used as diagnostic biomarkers for canine, and possibly also human, autoimmune disease. Nature Publishing Group UK 2018-03-19 /pmc/articles/PMC5859008/ /pubmed/29556082 http://dx.doi.org/10.1038/s41598-018-23034-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bremer, Hanna D.
Landegren, Nils
Sjöberg, Ronald
Hallgren, Åsa
Renneker, Stefanie
Lattwein, Erik
Leonard, Dag
Eloranta, Maija-Leena
Rönnblom, Lars
Nordmark, Gunnel
Nilsson, Peter
Andersson, Göran
Lilliehöök, Inger
Lindblad-Toh, Kerstin
Kämpe, Olle
Hansson-Hamlin, Helene
ILF2 and ILF3 are autoantigens in canine systemic autoimmune disease
title ILF2 and ILF3 are autoantigens in canine systemic autoimmune disease
title_full ILF2 and ILF3 are autoantigens in canine systemic autoimmune disease
title_fullStr ILF2 and ILF3 are autoantigens in canine systemic autoimmune disease
title_full_unstemmed ILF2 and ILF3 are autoantigens in canine systemic autoimmune disease
title_short ILF2 and ILF3 are autoantigens in canine systemic autoimmune disease
title_sort ilf2 and ilf3 are autoantigens in canine systemic autoimmune disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859008/
https://www.ncbi.nlm.nih.gov/pubmed/29556082
http://dx.doi.org/10.1038/s41598-018-23034-w
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