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Characterization of immunogenic Neu5Gc in bioprosthetic heart valves

dc.contributor.authorMoshe Reuven, Eliran
dc.contributor.authorLeviatan Ben-Arye, Shani
dc.contributor.authorMarshanski, Tal
dc.contributor.authorBreimer, Michael E.
dc.contributor.authorYu, Hai
dc.contributor.authorFellah-Hebia, Imen
dc.contributor.authorRoussel, Jean-Christian
dc.contributor.authorCosta Vallés, Cristina
dc.contributor.authorGalinanes, Manuel
dc.contributor.authorMáñez Mendiluce, Rafael
dc.contributor.authorTourneau, Thierry Le
dc.contributor.authorSoulillou, Jean Paul
dc.contributor.authorCozzi, Emanuele
dc.contributor.authorChen, Xi
dc.contributor.authorPadler-Karavani, Vered
dc.date.accessioned2018-10-29T14:30:39Z
dc.date.available2018-10-29T14:30:39Z
dc.date.issued2016-09-01
dc.date.updated2018-07-24T12:17:33Z
dc.description.abstractBackground: The two common sialic acids (Sias) in mammals are N-acetylneuraminic acid (Neu5Ac) and its hydroxylated form N-glycolylneuraminic acid (Neu5Gc). Unlike most mammals, humans cannot synthesize Neu5Gc that is considered foreign and recognized by circulating antibodies. Thus, Neu5Gc is a potential xenogenic carbohydrate antigen in bioprosthetic heart valves (BHV) that tend to deteriorate in time within human patients. Methods: We investigated Neu5Gc expression in non-engineered animal-derived cardiac tissues and in clinically used commercial BHV, and evaluated Neu5Gc immunogenicity on BHV through recognition by human anti-Neu5Gc IgG. Results: Neu5Gc was detected by immunohistochemistry in porcine aortic valves and in porcine and bovine pericardium. Qualitative analysis of Sia linkages revealed Siaa2-3> Siaa2-6 on porcine/bovine pericardium while the opposite in porcine aortic/pulmonary valve cusps. Similarly, six commercial BHV containing either porcine aortic valve or porcine/bovine/equine pericardium revealed Siaa2-3> Siaa2-6 expression. Quantitative analysis of Sia by HPLC showed porcine/bovine pericardium express 4-fold higher Neu5Gc levels compared to the porcine aortic/pulmonary valves, with Neu5Ac at 6-fold over Neu5Gc. Likewise, Neu5Gc was expressed on commercial BHV (186.3 +/- 16.9 pmol Sia/mu g protein), with Neu5Ac at 8-fold over Neu5Gc. Affinity-purified human anti-Neu5Gc IgG showing high specificity toward Neu5Gc-glycans (with no binding to Neu5Ac-glycans) on a glycan microarray, strongly bound to all tested commercial BHV, demonstrating Neu5Gc immune recognition in cardiac xenografts. Conclusions: We conclusively demonstrated Neu5Gc expression in native cardiac tissues, as well as in six commercial BHV. These Neu5Gc xeno-antigens were recognized by human anti-Neu5Gc IgG, supporting their immunogenicity. Altogether, these findings suggest BHV-Neu5Gc/anti-Neu5Gc may play a role in valve deterioration warranting further investigation.
dc.format.extent24 p.
dc.format.mimetypeapplication/pdf
dc.identifier.pmid27610947
dc.identifier.urihttps://hdl.handle.net/2445/125706
dc.language.isoeng
dc.publisherWiley
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1111/xen.12260
dc.relation.ispartofXenotransplantation, 2016, vol. 23, num. 5, p. 381-392
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/327726/EU//XENO-AUTOANTIBODIES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/603049/EU//TRANSLINK
dc.relation.urihttps://doi.org/10.1111/xen.12260
dc.rights(c) John Wiley and Sons, 2016
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationTrasplantament d'òrgans
dc.subject.classificationMalalties del cor
dc.subject.otherTransplantation of organs
dc.subject.otherHeart diseases
dc.titleCharacterization of immunogenic Neu5Gc in bioprosthetic heart valves
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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