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mCRP as a Biomarker of Adult-Onset Still’s Disease: Quantification of mCRP by ELISA

BACKGROUND: C-reactive protein (CRP) is a dynamic protein that undergoes conformational changes between circulating native pentameric CRP (pCRP), pentameric symmetrical forms (pCRP*) and monomeric (or modified) CRP (mCRP) forms. mCRP exhibits strong pro-inflammatory activity and activates platelets,...

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Autores principales: Fujita, Chitose, Sakurai, Yasuo, Yasuda, Yuki, Homma, Rino, Huang, Cheng-Long, Fujita, Masaaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284222/
https://www.ncbi.nlm.nih.gov/pubmed/35844576
http://dx.doi.org/10.3389/fimmu.2022.938173
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author Fujita, Chitose
Sakurai, Yasuo
Yasuda, Yuki
Homma, Rino
Huang, Cheng-Long
Fujita, Masaaki
author_facet Fujita, Chitose
Sakurai, Yasuo
Yasuda, Yuki
Homma, Rino
Huang, Cheng-Long
Fujita, Masaaki
author_sort Fujita, Chitose
collection PubMed
description BACKGROUND: C-reactive protein (CRP) is a dynamic protein that undergoes conformational changes between circulating native pentameric CRP (pCRP), pentameric symmetrical forms (pCRP*) and monomeric (or modified) CRP (mCRP) forms. mCRP exhibits strong pro-inflammatory activity and activates platelets, leukocytes, and endothelial cells. Abundant deposition of mCRP in inflamed tissues plays a role in several disease conditions, such as ischemia/reperfusion injury, Alzheimer’s disease, and cardiovascular disease. Although pCRP is typically quantified rather than mCRP for clinical purposes, mCRP may be a more appropriate disease marker of inflammatory diseases. Therefore, simple methods for quantifying mCRP are needed. METHODS: We developed a specific enzyme-linked immunosorbent assay (ELISA) to measure plasma levels of mCRP. Plasma mCRP concentration was measured in patients with adult-onset Still’s disease (AOSD) (n=20), polymyalgia rheumatica (PMR) (n=20), rheumatoid arthritis (RA) (n=30), infection (n=50), and in control subjects (n=30) using the developed ELISA. RESULTS: We demonstrated that mCRP is elevated in some inflammatory autoimmune diseases, particularly AOSD. The mCRP concentration was also significantly higher among AOSD patients than RA, PMR patients and controls (477 ng/ml, 77 ng/ml, 186 ng/ml, and 1.2 ng/ml, respectively). Also, the mCRP (×1,000)/pCRP ratio was significantly higher among AOSD patients than RA, PMR, and infection patients (3.5, 0.6, 1,6, and 2.0, respectively). CONCLUSION: The plasma mCRP levels are elevated in some autoimmune diseases, particularly AOSD. The plasma mCRP levels may therefore be a potentially useful biomarker for AOSD.
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spelling pubmed-92842222022-07-16 mCRP as a Biomarker of Adult-Onset Still’s Disease: Quantification of mCRP by ELISA Fujita, Chitose Sakurai, Yasuo Yasuda, Yuki Homma, Rino Huang, Cheng-Long Fujita, Masaaki Front Immunol Immunology BACKGROUND: C-reactive protein (CRP) is a dynamic protein that undergoes conformational changes between circulating native pentameric CRP (pCRP), pentameric symmetrical forms (pCRP*) and monomeric (or modified) CRP (mCRP) forms. mCRP exhibits strong pro-inflammatory activity and activates platelets, leukocytes, and endothelial cells. Abundant deposition of mCRP in inflamed tissues plays a role in several disease conditions, such as ischemia/reperfusion injury, Alzheimer’s disease, and cardiovascular disease. Although pCRP is typically quantified rather than mCRP for clinical purposes, mCRP may be a more appropriate disease marker of inflammatory diseases. Therefore, simple methods for quantifying mCRP are needed. METHODS: We developed a specific enzyme-linked immunosorbent assay (ELISA) to measure plasma levels of mCRP. Plasma mCRP concentration was measured in patients with adult-onset Still’s disease (AOSD) (n=20), polymyalgia rheumatica (PMR) (n=20), rheumatoid arthritis (RA) (n=30), infection (n=50), and in control subjects (n=30) using the developed ELISA. RESULTS: We demonstrated that mCRP is elevated in some inflammatory autoimmune diseases, particularly AOSD. The mCRP concentration was also significantly higher among AOSD patients than RA, PMR patients and controls (477 ng/ml, 77 ng/ml, 186 ng/ml, and 1.2 ng/ml, respectively). Also, the mCRP (×1,000)/pCRP ratio was significantly higher among AOSD patients than RA, PMR, and infection patients (3.5, 0.6, 1,6, and 2.0, respectively). CONCLUSION: The plasma mCRP levels are elevated in some autoimmune diseases, particularly AOSD. The plasma mCRP levels may therefore be a potentially useful biomarker for AOSD. Frontiers Media S.A. 2022-07-01 /pmc/articles/PMC9284222/ /pubmed/35844576 http://dx.doi.org/10.3389/fimmu.2022.938173 Text en Copyright © 2022 Fujita, Sakurai, Yasuda, Homma, Huang and Fujita https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Fujita, Chitose
Sakurai, Yasuo
Yasuda, Yuki
Homma, Rino
Huang, Cheng-Long
Fujita, Masaaki
mCRP as a Biomarker of Adult-Onset Still’s Disease: Quantification of mCRP by ELISA
title mCRP as a Biomarker of Adult-Onset Still’s Disease: Quantification of mCRP by ELISA
title_full mCRP as a Biomarker of Adult-Onset Still’s Disease: Quantification of mCRP by ELISA
title_fullStr mCRP as a Biomarker of Adult-Onset Still’s Disease: Quantification of mCRP by ELISA
title_full_unstemmed mCRP as a Biomarker of Adult-Onset Still’s Disease: Quantification of mCRP by ELISA
title_short mCRP as a Biomarker of Adult-Onset Still’s Disease: Quantification of mCRP by ELISA
title_sort mcrp as a biomarker of adult-onset still’s disease: quantification of mcrp by elisa
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284222/
https://www.ncbi.nlm.nih.gov/pubmed/35844576
http://dx.doi.org/10.3389/fimmu.2022.938173
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