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Cell-bound complement activation products in SLE
Diagnosis of SLE is based on clinical manifestations and laboratory findings. Timely diagnosis and treatment are important to control disease activity and prevent organ damage. However, diagnosis is challenging because of the heterogeneity in clinical signs and symptoms, and also because the disease...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704741/ https://www.ncbi.nlm.nih.gov/pubmed/29214038 http://dx.doi.org/10.1136/lupus-2017-000236 |
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author | Ramsey-Goldman, Rosalind Li, Jian Dervieux, Thierry Alexander, Roberta Vezza |
author_facet | Ramsey-Goldman, Rosalind Li, Jian Dervieux, Thierry Alexander, Roberta Vezza |
author_sort | Ramsey-Goldman, Rosalind |
collection | PubMed |
description | Diagnosis of SLE is based on clinical manifestations and laboratory findings. Timely diagnosis and treatment are important to control disease activity and prevent organ damage. However, diagnosis is challenging because of the heterogeneity in clinical signs and symptoms, and also because the disease presents with alternating periods of flare and quiescence. As SLE is an autoimmune disease characterised by the formation of autoantibodies, diagnostic immunology laboratory tests for detecting and quantifying autoantibodies are commonly used for the diagnosis and classification of SLE. These include ANA, anti-double-stranded DNA antibodies and anti-Smith antibodies, together with other antibodies such as antiphospholipid or anti-Cq1. Complement proteins C3 and C4 are commonly measured in patients with SLE, but their serum levels do not necessarily reflect complement activation. Cell-bound complement activation products (CB-CAPs) are fragments formed upon complement activation that bind covalently to haematopoietic cells. This review focuses on the complement system and, in particular, on CB-CAPs as biomarkers for the diagnosis and monitoring of SLE, vis-à-vis complement proteins and other biomarkers of complement activation. |
format | Online Article Text |
id | pubmed-5704741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-57047412017-12-06 Cell-bound complement activation products in SLE Ramsey-Goldman, Rosalind Li, Jian Dervieux, Thierry Alexander, Roberta Vezza Lupus Sci Med Review Diagnosis of SLE is based on clinical manifestations and laboratory findings. Timely diagnosis and treatment are important to control disease activity and prevent organ damage. However, diagnosis is challenging because of the heterogeneity in clinical signs and symptoms, and also because the disease presents with alternating periods of flare and quiescence. As SLE is an autoimmune disease characterised by the formation of autoantibodies, diagnostic immunology laboratory tests for detecting and quantifying autoantibodies are commonly used for the diagnosis and classification of SLE. These include ANA, anti-double-stranded DNA antibodies and anti-Smith antibodies, together with other antibodies such as antiphospholipid or anti-Cq1. Complement proteins C3 and C4 are commonly measured in patients with SLE, but their serum levels do not necessarily reflect complement activation. Cell-bound complement activation products (CB-CAPs) are fragments formed upon complement activation that bind covalently to haematopoietic cells. This review focuses on the complement system and, in particular, on CB-CAPs as biomarkers for the diagnosis and monitoring of SLE, vis-à-vis complement proteins and other biomarkers of complement activation. BMJ Publishing Group 2017-08-21 /pmc/articles/PMC5704741/ /pubmed/29214038 http://dx.doi.org/10.1136/lupus-2017-000236 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Review Ramsey-Goldman, Rosalind Li, Jian Dervieux, Thierry Alexander, Roberta Vezza Cell-bound complement activation products in SLE |
title | Cell-bound complement activation products in SLE |
title_full | Cell-bound complement activation products in SLE |
title_fullStr | Cell-bound complement activation products in SLE |
title_full_unstemmed | Cell-bound complement activation products in SLE |
title_short | Cell-bound complement activation products in SLE |
title_sort | cell-bound complement activation products in sle |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704741/ https://www.ncbi.nlm.nih.gov/pubmed/29214038 http://dx.doi.org/10.1136/lupus-2017-000236 |
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