Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783307729900666880 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5859008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT bremerhannad ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT landegrennils ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT sjobergronald ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT hallgrenasa ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT rennekerstefanie ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT lattweinerik ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT leonarddag ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT elorantamaijaleena ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT ronnblomlars ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT nordmarkgunnel ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT nilssonpeter ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT anderssongoran ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT lilliehookinger ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT lindbladtohkerstin ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT kampeolle ilf2andilf3areautoantigensincaninesystemicautoimmunedisease AT hanssonhamlinhelene ilf2andilf3areautoantigensincaninesystemicautoimmunedisease |