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Soluble glycoprotein VI, a specific marker of platelet activation is increased in the plasma of subjects with seropositive rheumatoid arthritis
OBJECTIVES: Anti-citrullinated protein antibodies (ACPA) have been shown to cause platelet activation in vitro, through the low-affinity immunoglobulin G (IgG) receptor (FcγRIIa) on platelets. Platelet activation via engagement of FcγRIIa results in proteolytic cleavage and shedding of platelet spec...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687752/ https://www.ncbi.nlm.nih.gov/pubmed/29141000 http://dx.doi.org/10.1371/journal.pone.0188027 |
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author | Stack, John R. Madigan, Anne Helbert, Laura Dunne, Eimear Gardiner, Elizabeth E. Andrews, Robert K. Finan, Roisin Smyth, Elizabeth Kenny, Dermot McCarthy, Geraldine M. |
author_facet | Stack, John R. Madigan, Anne Helbert, Laura Dunne, Eimear Gardiner, Elizabeth E. Andrews, Robert K. Finan, Roisin Smyth, Elizabeth Kenny, Dermot McCarthy, Geraldine M. |
author_sort | Stack, John R. |
collection | PubMed |
description | OBJECTIVES: Anti-citrullinated protein antibodies (ACPA) have been shown to cause platelet activation in vitro, through the low-affinity immunoglobulin G (IgG) receptor (FcγRIIa) on platelets. Platelet activation via engagement of FcγRIIa results in proteolytic cleavage and shedding of platelet specific glycoprotein VI (GPVI) which can be detected in the plasma as soluble GPVI (sGPVI). We hypothesized that plasma levels of sGPVI would be increased among patients with seropositive RA as a consequence of antibody-induced platelet activation and GPVI shedding. METHODS: Samples from 84 patients with RA (65 seropositive and 19 seronegative) and 67 healthy controls were collected prospectively and analysed for sGPVI using a standardised ELISA. RESULTS: Patients with seropositive RA had significantly higher levels of sGPVI compared to seronegative RA and controls. Median (IQR) sGPVI levels were 4.2 ng/ml (3.2, 8.0) in seropositve RA, 2.2 ng/ml (1.5, 3.5) in seronegative RA and 2.2 ng/ml (1.6, 3.4) in controls (p<0.0001). sGPVI levels correlated with ACPA titres (r = 0.32, p = 0.0026) and with RF titres (r = 0.48, p<0.0001). CONCLUSION: Plasma sGPVI, a specific marker of platelet activation is increased among patients with seropositive RA. |
format | Online Article Text |
id | pubmed-5687752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56877522017-11-30 Soluble glycoprotein VI, a specific marker of platelet activation is increased in the plasma of subjects with seropositive rheumatoid arthritis Stack, John R. Madigan, Anne Helbert, Laura Dunne, Eimear Gardiner, Elizabeth E. Andrews, Robert K. Finan, Roisin Smyth, Elizabeth Kenny, Dermot McCarthy, Geraldine M. PLoS One Research Article OBJECTIVES: Anti-citrullinated protein antibodies (ACPA) have been shown to cause platelet activation in vitro, through the low-affinity immunoglobulin G (IgG) receptor (FcγRIIa) on platelets. Platelet activation via engagement of FcγRIIa results in proteolytic cleavage and shedding of platelet specific glycoprotein VI (GPVI) which can be detected in the plasma as soluble GPVI (sGPVI). We hypothesized that plasma levels of sGPVI would be increased among patients with seropositive RA as a consequence of antibody-induced platelet activation and GPVI shedding. METHODS: Samples from 84 patients with RA (65 seropositive and 19 seronegative) and 67 healthy controls were collected prospectively and analysed for sGPVI using a standardised ELISA. RESULTS: Patients with seropositive RA had significantly higher levels of sGPVI compared to seronegative RA and controls. Median (IQR) sGPVI levels were 4.2 ng/ml (3.2, 8.0) in seropositve RA, 2.2 ng/ml (1.5, 3.5) in seronegative RA and 2.2 ng/ml (1.6, 3.4) in controls (p<0.0001). sGPVI levels correlated with ACPA titres (r = 0.32, p = 0.0026) and with RF titres (r = 0.48, p<0.0001). CONCLUSION: Plasma sGPVI, a specific marker of platelet activation is increased among patients with seropositive RA. Public Library of Science 2017-11-15 /pmc/articles/PMC5687752/ /pubmed/29141000 http://dx.doi.org/10.1371/journal.pone.0188027 Text en © 2017 Stack et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Stack, John R. Madigan, Anne Helbert, Laura Dunne, Eimear Gardiner, Elizabeth E. Andrews, Robert K. Finan, Roisin Smyth, Elizabeth Kenny, Dermot McCarthy, Geraldine M. Soluble glycoprotein VI, a specific marker of platelet activation is increased in the plasma of subjects with seropositive rheumatoid arthritis |
title | Soluble glycoprotein VI, a specific marker of platelet activation is increased in the plasma of subjects with seropositive rheumatoid arthritis |
title_full | Soluble glycoprotein VI, a specific marker of platelet activation is increased in the plasma of subjects with seropositive rheumatoid arthritis |
title_fullStr | Soluble glycoprotein VI, a specific marker of platelet activation is increased in the plasma of subjects with seropositive rheumatoid arthritis |
title_full_unstemmed | Soluble glycoprotein VI, a specific marker of platelet activation is increased in the plasma of subjects with seropositive rheumatoid arthritis |
title_short | Soluble glycoprotein VI, a specific marker of platelet activation is increased in the plasma of subjects with seropositive rheumatoid arthritis |
title_sort | soluble glycoprotein vi, a specific marker of platelet activation is increased in the plasma of subjects with seropositive rheumatoid arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687752/ https://www.ncbi.nlm.nih.gov/pubmed/29141000 http://dx.doi.org/10.1371/journal.pone.0188027 |
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