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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...

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Autores principales: Otteby, Kaisa E, Holmquist, Emelie, Saxne, Tore, Heinegård, Dick, Hesselstrand, Roger, Blom, Anna M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
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.
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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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