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Cartilage oligomeric matrix protein-induced complement activation in systemic sclerosis
INTRODUCTION: Complexes between cartilage oligomeric matrix protein (COMP) and the complement activation product C3b have been found in the circulation of patients with rheumatoid arthritis and systemic lupus erythematosus. In systemic sclerosis (SSc) COMP expression in the skin is upregulated both...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978716/ https://www.ncbi.nlm.nih.gov/pubmed/24330664 http://dx.doi.org/10.1186/ar4410 |
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author | Otteby, Kaisa E Holmquist, Emelie Saxne, Tore Heinegård, Dick Hesselstrand, Roger Blom, Anna M |
author_facet | Otteby, Kaisa E Holmquist, Emelie Saxne, Tore Heinegård, Dick Hesselstrand, Roger Blom, Anna M |
author_sort | Otteby, Kaisa E |
collection | PubMed |
description | INTRODUCTION: Complexes between cartilage oligomeric matrix protein (COMP) and the complement activation product C3b have been found in the circulation of patients with rheumatoid arthritis and systemic lupus erythematosus. In systemic sclerosis (SSc) COMP expression in the skin is upregulated both in lesional and non-lesional skin, which is also reflected in an increased amount of circulating COMP. We investigated the presence of COMP-C3b complexes in serum and skin biopsies of patients with SSc. METHODS: The presence of COMP and COMP-C3b complexes in the serum of 80 patients with limited cutaneous SSc (lcSSc, n = 40) and diffuse cutaneous SSc (dcSSc, n = 40) and 97 healthy controls was measured by ELISA and correlated to different clinical parameters. Samples were collected both at baseline and after three to five years to assess longitudinal changes in COMP-C3b complex levels. Furthermore, skin biopsies from seven patients with dcSSc and three healthy controls were analyzed for expression of COMP and deposition of C3b and IgG. RESULTS: Serum levels of COMP-C3b were found to be elevated in both dcSSc and lcSSc compared to healthy controls and decreased at the second measurement in patients on immunosuppressive therapy. No co-localization of COMP and C3b was found in the skin biopsies, indicating that the COMP-C3b complexes are formed upon release of COMP into the circulation. CONCLUSION: COMP-C3b complexes are found in the serum of patients with SSc. The lack of co-localization between COMP and C3b in the skin suggests that COMP does not drive complement activation in the skin in SSc. |
format | Online Article Text |
id | pubmed-3978716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39787162014-04-09 Cartilage oligomeric matrix protein-induced complement activation in systemic sclerosis Otteby, Kaisa E Holmquist, Emelie Saxne, Tore Heinegård, Dick Hesselstrand, Roger Blom, Anna M Arthritis Res Ther Research Article INTRODUCTION: Complexes between cartilage oligomeric matrix protein (COMP) and the complement activation product C3b have been found in the circulation of patients with rheumatoid arthritis and systemic lupus erythematosus. In systemic sclerosis (SSc) COMP expression in the skin is upregulated both in lesional and non-lesional skin, which is also reflected in an increased amount of circulating COMP. We investigated the presence of COMP-C3b complexes in serum and skin biopsies of patients with SSc. METHODS: The presence of COMP and COMP-C3b complexes in the serum of 80 patients with limited cutaneous SSc (lcSSc, n = 40) and diffuse cutaneous SSc (dcSSc, n = 40) and 97 healthy controls was measured by ELISA and correlated to different clinical parameters. Samples were collected both at baseline and after three to five years to assess longitudinal changes in COMP-C3b complex levels. Furthermore, skin biopsies from seven patients with dcSSc and three healthy controls were analyzed for expression of COMP and deposition of C3b and IgG. RESULTS: Serum levels of COMP-C3b were found to be elevated in both dcSSc and lcSSc compared to healthy controls and decreased at the second measurement in patients on immunosuppressive therapy. No co-localization of COMP and C3b was found in the skin biopsies, indicating that the COMP-C3b complexes are formed upon release of COMP into the circulation. CONCLUSION: COMP-C3b complexes are found in the serum of patients with SSc. The lack of co-localization between COMP and C3b in the skin suggests that COMP does not drive complement activation in the skin in SSc. BioMed Central 2013 2013-12-13 /pmc/articles/PMC3978716/ /pubmed/24330664 http://dx.doi.org/10.1186/ar4410 Text en Copyright © 2013 Otteby et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Otteby, Kaisa E Holmquist, Emelie Saxne, Tore Heinegård, Dick Hesselstrand, Roger Blom, Anna M Cartilage oligomeric matrix protein-induced complement activation in systemic sclerosis |
title | Cartilage oligomeric matrix protein-induced complement activation in systemic sclerosis |
title_full | Cartilage oligomeric matrix protein-induced complement activation in systemic sclerosis |
title_fullStr | Cartilage oligomeric matrix protein-induced complement activation in systemic sclerosis |
title_full_unstemmed | Cartilage oligomeric matrix protein-induced complement activation in systemic sclerosis |
title_short | Cartilage oligomeric matrix protein-induced complement activation in systemic sclerosis |
title_sort | cartilage oligomeric matrix protein-induced complement activation in systemic sclerosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978716/ https://www.ncbi.nlm.nih.gov/pubmed/24330664 http://dx.doi.org/10.1186/ar4410 |
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