Enzyme-linked immunosorbent assay (ELISAs) for metalloproteinase derived type II collagen neoepitope, CIIM—Increased serum CIIM in subjects with severe radiographic osteoarthritis

In joint degenerative diseases, the collagens are degraded by matrix metalloproteinases and protein fragments are released to serum as potential biomarkers. A collagen type II specific neoepitope, CIIM, was identified (…RDGAAG 1053) by mass spectrometry. Two ELISAs against the neoepitope were develo...

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Published inClinical biochemistry Vol. 44; no. 5; pp. 423 - 429
Main Authors Bay-Jensen, Anne-Christine, Liu, Qi, Byrjalsen, Inger, Li, Yi, Wang, Jianxia, Pedersen, Christian, Leeming, Diana J., Dam, Erik B., Zheng, Qinlong, Qvist, Per, Karsdal, Morten A.
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LanguageEnglish
Published Amsterdam Elsevier Inc 01.04.2011
Elsevier
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Abstract In joint degenerative diseases, the collagens are degraded by matrix metalloproteinases and protein fragments are released to serum as potential biomarkers. A collagen type II specific neoepitope, CIIM, was identified (…RDGAAG 1053) by mass spectrometry. Two ELISAs against the neoepitope were developed. CIIM was measured in cartilage explants in the presence or absence of protease inhibitors. CIIM was measured in OA synovial fluid ( n = 51) and serum ( n = 156). Knee OA was graded by standard Kellgren–Lawrence (KL) score. The ELISAs showed good technical performance; CV%, < 13%. CIIM release from cartilage explants was blocked by the MMP inhibitor. CIIM was detected in synovial fluid. Furthermore, serum CIIM levels were significantly higher ( P < 0.05) in those individuals with mild or severe OA than in those with no OA. We developed a new biomarker for joint degenerative diseases, which we demonstrated was derived from MMP-degraded type II collagen.
AbstractList In joint degenerative diseases, the collagens are degraded by matrix metalloproteinases and protein fragments are released to serum as potential biomarkers. A collagen type II specific neoepitope, CIIM, was identified (…RDGAAG 1053) by mass spectrometry. Two ELISAs against the neoepitope were developed. CIIM was measured in cartilage explants in the presence or absence of protease inhibitors. CIIM was measured in OA synovial fluid ( n = 51) and serum ( n = 156). Knee OA was graded by standard Kellgren–Lawrence (KL) score. The ELISAs showed good technical performance; CV%, < 13%. CIIM release from cartilage explants was blocked by the MMP inhibitor. CIIM was detected in synovial fluid. Furthermore, serum CIIM levels were significantly higher ( P < 0.05) in those individuals with mild or severe OA than in those with no OA. We developed a new biomarker for joint degenerative diseases, which we demonstrated was derived from MMP-degraded type II collagen.
In joint degenerative diseases, the collagens are degraded by matrix metalloproteinases and protein fragments are released to serum as potential biomarkers. A collagen type II specific neoepitope, CIIM, was identified (…RDGAAG(1053)) by mass spectrometry. Two ELISAs against the neoepitope were developed. CIIM was measured in cartilage explants in the presence or absence of protease inhibitors. CIIM was measured in OA synovial fluid (n=51) and serum (n=156). Knee OA was graded by standard Kellgren-Lawrence (KL) score. The ELISAs showed good technical performance; CV%, <13%. CIIM release from cartilage explants was blocked by the MMP inhibitor. CIIM was detected in synovial fluid. Furthermore, serum CIIM levels were significantly higher (P<0.05) in those individuals with mild or severe OA than in those with no OA. We developed a new biomarker for joint degenerative diseases, which we demonstrated was derived from MMP-degraded type II collagen.
In joint degenerative diseases, the collagens are degraded by matrix metalloproteinases and protein fragments are released to serum as potential biomarkers.OBJECTIVESIn joint degenerative diseases, the collagens are degraded by matrix metalloproteinases and protein fragments are released to serum as potential biomarkers.A collagen type II specific neoepitope, CIIM, was identified (…RDGAAG(1053)) by mass spectrometry. Two ELISAs against the neoepitope were developed. CIIM was measured in cartilage explants in the presence or absence of protease inhibitors. CIIM was measured in OA synovial fluid (n=51) and serum (n=156). Knee OA was graded by standard Kellgren-Lawrence (KL) score.METHODSA collagen type II specific neoepitope, CIIM, was identified (…RDGAAG(1053)) by mass spectrometry. Two ELISAs against the neoepitope were developed. CIIM was measured in cartilage explants in the presence or absence of protease inhibitors. CIIM was measured in OA synovial fluid (n=51) and serum (n=156). Knee OA was graded by standard Kellgren-Lawrence (KL) score.The ELISAs showed good technical performance; CV%, <13%. CIIM release from cartilage explants was blocked by the MMP inhibitor. CIIM was detected in synovial fluid. Furthermore, serum CIIM levels were significantly higher (P<0.05) in those individuals with mild or severe OA than in those with no OA.RESULTSThe ELISAs showed good technical performance; CV%, <13%. CIIM release from cartilage explants was blocked by the MMP inhibitor. CIIM was detected in synovial fluid. Furthermore, serum CIIM levels were significantly higher (P<0.05) in those individuals with mild or severe OA than in those with no OA.We developed a new biomarker for joint degenerative diseases, which we demonstrated was derived from MMP-degraded type II collagen.CONCLUSIONWe developed a new biomarker for joint degenerative diseases, which we demonstrated was derived from MMP-degraded type II collagen.
Author Zheng, Qinlong
Bay-Jensen, Anne-Christine
Leeming, Diana J.
Wang, Jianxia
Qvist, Per
Pedersen, Christian
Karsdal, Morten A.
Byrjalsen, Inger
Li, Yi
Dam, Erik B.
Liu, Qi
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  surname: Liu
  fullname: Liu, Qi
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  surname: Byrjalsen
  fullname: Byrjalsen, Inger
  organization: Cartilage Biology and Biomarkers R&D, Nordic Bioscience, Herlev, Denmark
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  givenname: Yi
  surname: Li
  fullname: Li, Yi
  organization: Assay Development, Nordic Bioscience China, Beijing, PR China
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  surname: Wang
  fullname: Wang, Jianxia
  organization: Assay Development, Nordic Bioscience China, Beijing, PR China
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  fullname: Pedersen, Christian
  organization: Klinik Farsoe, Ortopaedkirugien, Farsoe, Denmark
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  givenname: Diana J.
  surname: Leeming
  fullname: Leeming, Diana J.
  organization: Fibrosis Biology and Biomarker R&D, Nordic Bioscience, Herlev, Denmark
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  givenname: Erik B.
  surname: Dam
  fullname: Dam, Erik B.
  organization: Synarc Imaging Technologies, Herlev, Denmark
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  givenname: Qinlong
  surname: Zheng
  fullname: Zheng, Qinlong
  organization: Assay Development, Nordic Bioscience China, Beijing, PR China
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  surname: Qvist
  fullname: Qvist, Per
  organization: Cartilage Biology and Biomarkers R&D, Nordic Bioscience, Herlev, Denmark
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  surname: Karsdal
  fullname: Karsdal, Morten A.
  organization: Cartilage Biology and Biomarkers R&D, Nordic Bioscience, Herlev, Denmark
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IsPeerReviewed true
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Issue 5
Keywords MMP
Cartilage
OA
Neoepitope
Serum CIIM
JSN
Metalloproteinase
Type II collagen
Osteoarthritis
ECM
ELISA
Diseases of the osteoarticular system
Metalloendopeptidases
Clinical biology
Serum
Degenerative disease
Human
Radiodiagnosis
Enzyme
Exploration
Collagen type II
Enzyme immunoassay
Radiography
Peptidases
Articular cartilage
Arthropathy
Hydrolases
Severe
ELISA assay
Language English
License https://www.elsevier.com/tdm/userlicense/1.0
CC BY 4.0
Copyright © 2011 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
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Snippet In joint degenerative diseases, the collagens are degraded by matrix metalloproteinases and protein fragments are released to serum as potential biomarkers. A...
In joint degenerative diseases, the collagens are degraded by matrix metalloproteinases and protein fragments are released to serum as potential...
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StartPage 423
SubjectTerms Aged
Aged, 80 and over
Biological and medical sciences
Cartilage
Collagen Type II - blood
Diseases of the osteoarticular system
ELISA
Enzyme-Linked Immunosorbent Assay - methods
Female
Humans
Investigative techniques, diagnostic techniques (general aspects)
Male
Medical sciences
Metalloproteases - blood
Metalloproteinase
Middle Aged
Miscellaneous. Osteoarticular involvement in other diseases
Neoepitope
Osteoarthritis
Osteoarthritis - blood
Osteoarthritis - enzymology
Serum CIIM
Type II collagen
Title Enzyme-linked immunosorbent assay (ELISAs) for metalloproteinase derived type II collagen neoepitope, CIIM—Increased serum CIIM in subjects with severe radiographic osteoarthritis
URI https://dx.doi.org/10.1016/j.clinbiochem.2011.01.001
https://www.ncbi.nlm.nih.gov/pubmed/21223960
https://www.proquest.com/docview/857814956
Volume 44
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