Cargando…

Antigenicity of Bovine Pericardium Determined by a Novel Immunoproteomic Approach

Despite bovine pericardium (BP) being the primary biomaterial used in heart valve bioprostheses, recipient graft-specific immune responses remain a significant cause of graft failure. Consequently, tissue antigenicity remains the principal barrier for expanding use of such biomaterials in clinical p...

Descripción completa

Detalles Bibliográficos
Autores principales: Gates, Katherine V., Dalgliesh, Ailsa J., Griffiths, Leigh G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446425/
https://www.ncbi.nlm.nih.gov/pubmed/28550302
http://dx.doi.org/10.1038/s41598-017-02719-8
_version_ 1783239091603636224
author Gates, Katherine V.
Dalgliesh, Ailsa J.
Griffiths, Leigh G.
author_facet Gates, Katherine V.
Dalgliesh, Ailsa J.
Griffiths, Leigh G.
author_sort Gates, Katherine V.
collection PubMed
description Despite bovine pericardium (BP) being the primary biomaterial used in heart valve bioprostheses, recipient graft-specific immune responses remain a significant cause of graft failure. Consequently, tissue antigenicity remains the principal barrier for expanding use of such biomaterials in clinical practice. We hypothesize that our understanding of BP antigenicity can be improved by application of a combined affinity chromatography shotgun immunoproteomic approach to identify antigens that have previously been overlooked. Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS) analysis of affinity chromatography purified antigens resulted in identification of 133 antigens. Most importantly, antigens were identified from all subcellular locations, including 18 integral membrane protein antigens. Critically, isoforms of several protein families were found to be antigenic suggesting the possibility that shared epitope domains may exist. Furthermore, proteins associated with immune, coagulation, and inflammatory pathways were over-represented, suggesting that these biological processes play a key role in antigenicity. This study brings to light important determinants of antigenicity in a clinically relevant xenogeneic biomaterial (i.e. BP) and further validates a rapid, high-throughput method for immunoproteomic antigen identification.
format Online
Article
Text
id pubmed-5446425
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-54464252017-05-30 Antigenicity of Bovine Pericardium Determined by a Novel Immunoproteomic Approach Gates, Katherine V. Dalgliesh, Ailsa J. Griffiths, Leigh G. Sci Rep Article Despite bovine pericardium (BP) being the primary biomaterial used in heart valve bioprostheses, recipient graft-specific immune responses remain a significant cause of graft failure. Consequently, tissue antigenicity remains the principal barrier for expanding use of such biomaterials in clinical practice. We hypothesize that our understanding of BP antigenicity can be improved by application of a combined affinity chromatography shotgun immunoproteomic approach to identify antigens that have previously been overlooked. Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS) analysis of affinity chromatography purified antigens resulted in identification of 133 antigens. Most importantly, antigens were identified from all subcellular locations, including 18 integral membrane protein antigens. Critically, isoforms of several protein families were found to be antigenic suggesting the possibility that shared epitope domains may exist. Furthermore, proteins associated with immune, coagulation, and inflammatory pathways were over-represented, suggesting that these biological processes play a key role in antigenicity. This study brings to light important determinants of antigenicity in a clinically relevant xenogeneic biomaterial (i.e. BP) and further validates a rapid, high-throughput method for immunoproteomic antigen identification. Nature Publishing Group UK 2017-05-26 /pmc/articles/PMC5446425/ /pubmed/28550302 http://dx.doi.org/10.1038/s41598-017-02719-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gates, Katherine V.
Dalgliesh, Ailsa J.
Griffiths, Leigh G.
Antigenicity of Bovine Pericardium Determined by a Novel Immunoproteomic Approach
title Antigenicity of Bovine Pericardium Determined by a Novel Immunoproteomic Approach
title_full Antigenicity of Bovine Pericardium Determined by a Novel Immunoproteomic Approach
title_fullStr Antigenicity of Bovine Pericardium Determined by a Novel Immunoproteomic Approach
title_full_unstemmed Antigenicity of Bovine Pericardium Determined by a Novel Immunoproteomic Approach
title_short Antigenicity of Bovine Pericardium Determined by a Novel Immunoproteomic Approach
title_sort antigenicity of bovine pericardium determined by a novel immunoproteomic approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446425/
https://www.ncbi.nlm.nih.gov/pubmed/28550302
http://dx.doi.org/10.1038/s41598-017-02719-8
work_keys_str_mv AT gateskatherinev antigenicityofbovinepericardiumdeterminedbyanovelimmunoproteomicapproach
AT dalglieshailsaj antigenicityofbovinepericardiumdeterminedbyanovelimmunoproteomicapproach
AT griffithsleighg antigenicityofbovinepericardiumdeterminedbyanovelimmunoproteomicapproach