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Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology

Systemic sclerosis represents a chronic connective tissue disease featuring fibrosis, vasculopathy and autoimmunity, affecting skin, multiple internal organs, and skeletal muscles. The vasculopathy is considered obliterative, but its pathogenesis is still poorly understood. This may partially be due...

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Autores principales: Siegert, Elise, Uruha, Akinori, Goebel, Hans-Hilmar, Preuße, Corinna, Casteleyn, Vincent, Kleefeld, Felix, Alten, Rieke, Burmester, Gerd R., Schneider, Udo, Höppner, Jakob, Hahn, Kathrin, Dittmayer, Carsten, Stenzel, Werner
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113184/
https://www.ncbi.nlm.nih.gov/pubmed/33864496
http://dx.doi.org/10.1007/s00401-021-02305-3
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author Siegert, Elise
Uruha, Akinori
Goebel, Hans-Hilmar
Preuße, Corinna
Casteleyn, Vincent
Kleefeld, Felix
Alten, Rieke
Burmester, Gerd R.
Schneider, Udo
Höppner, Jakob
Hahn, Kathrin
Dittmayer, Carsten
Stenzel, Werner
author_facet Siegert, Elise
Uruha, Akinori
Goebel, Hans-Hilmar
Preuße, Corinna
Casteleyn, Vincent
Kleefeld, Felix
Alten, Rieke
Burmester, Gerd R.
Schneider, Udo
Höppner, Jakob
Hahn, Kathrin
Dittmayer, Carsten
Stenzel, Werner
author_sort Siegert, Elise
collection PubMed
description Systemic sclerosis represents a chronic connective tissue disease featuring fibrosis, vasculopathy and autoimmunity, affecting skin, multiple internal organs, and skeletal muscles. The vasculopathy is considered obliterative, but its pathogenesis is still poorly understood. This may partially be due to limitations of conventional transmission electron microscopy previously being conducted only in single patients. The aim of our study was therefore to precisely characterize immune inflammatory features and capillary morphology of systemic sclerosis patients suffering from muscle weakness. In this study, we identified 18 individuals who underwent muscle biopsy because of muscle weakness and myalgia in a cohort of 367 systemic sclerosis patients. We performed detailed conventional and immunohistochemical analysis and large-scale electron microscopy by digitizing entire sections for in-depth ultrastructural analysis. Muscle biopsies of 12 of these 18 patients (67%) presented minimal features of myositis but clear capillary alteration, which we termed minimal myositis with capillary pathology (MMCP). Our study provides novel findings in systemic sclerosis-associated myositis. First, we identified a characteristic and specific morphological pattern termed MMCP in 67% of the cases, while the other 33% feature alterations characteristic of other overlap syndromes. This is also reflected by a relatively homogeneous clinical picture among MMCP patients. They have milder disease with little muscle weakness and a low prevalence of interstitial lung disease (20%) and diffuse skin involvement (10%) and no cases of either pulmonary arterial hypertension or renal crisis. Second, large-scale electron microscopy, introducing a new level of precision in ultrastructural analysis, revealed a characteristic capillary morphology with basement membrane thickening and reduplications, endothelial activation and pericyte proliferation. We provide open-access pan-and-zoom analysis to our datasets, enabling critical discussion and data mining. We clearly highlight characteristic capillary pathology in skeletal muscles of systemic sclerosis patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00401-021-02305-3.
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spelling pubmed-81131842021-05-13 Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology Siegert, Elise Uruha, Akinori Goebel, Hans-Hilmar Preuße, Corinna Casteleyn, Vincent Kleefeld, Felix Alten, Rieke Burmester, Gerd R. Schneider, Udo Höppner, Jakob Hahn, Kathrin Dittmayer, Carsten Stenzel, Werner Acta Neuropathol Original Paper Systemic sclerosis represents a chronic connective tissue disease featuring fibrosis, vasculopathy and autoimmunity, affecting skin, multiple internal organs, and skeletal muscles. The vasculopathy is considered obliterative, but its pathogenesis is still poorly understood. This may partially be due to limitations of conventional transmission electron microscopy previously being conducted only in single patients. The aim of our study was therefore to precisely characterize immune inflammatory features and capillary morphology of systemic sclerosis patients suffering from muscle weakness. In this study, we identified 18 individuals who underwent muscle biopsy because of muscle weakness and myalgia in a cohort of 367 systemic sclerosis patients. We performed detailed conventional and immunohistochemical analysis and large-scale electron microscopy by digitizing entire sections for in-depth ultrastructural analysis. Muscle biopsies of 12 of these 18 patients (67%) presented minimal features of myositis but clear capillary alteration, which we termed minimal myositis with capillary pathology (MMCP). Our study provides novel findings in systemic sclerosis-associated myositis. First, we identified a characteristic and specific morphological pattern termed MMCP in 67% of the cases, while the other 33% feature alterations characteristic of other overlap syndromes. This is also reflected by a relatively homogeneous clinical picture among MMCP patients. They have milder disease with little muscle weakness and a low prevalence of interstitial lung disease (20%) and diffuse skin involvement (10%) and no cases of either pulmonary arterial hypertension or renal crisis. Second, large-scale electron microscopy, introducing a new level of precision in ultrastructural analysis, revealed a characteristic capillary morphology with basement membrane thickening and reduplications, endothelial activation and pericyte proliferation. We provide open-access pan-and-zoom analysis to our datasets, enabling critical discussion and data mining. We clearly highlight characteristic capillary pathology in skeletal muscles of systemic sclerosis patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00401-021-02305-3. Springer Berlin Heidelberg 2021-04-17 2021 /pmc/articles/PMC8113184/ /pubmed/33864496 http://dx.doi.org/10.1007/s00401-021-02305-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Siegert, Elise
Uruha, Akinori
Goebel, Hans-Hilmar
Preuße, Corinna
Casteleyn, Vincent
Kleefeld, Felix
Alten, Rieke
Burmester, Gerd R.
Schneider, Udo
Höppner, Jakob
Hahn, Kathrin
Dittmayer, Carsten
Stenzel, Werner
Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology
title Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology
title_full Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology
title_fullStr Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology
title_full_unstemmed Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology
title_short Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology
title_sort systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113184/
https://www.ncbi.nlm.nih.gov/pubmed/33864496
http://dx.doi.org/10.1007/s00401-021-02305-3
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