TY - JOUR
T1 - Antibody and Cellular Immune Responses in Old α1,3-Galactosyltransferase-Knockout Mice Implanted with Bioprosthetic Heart Valve Tissues
AU - Casós, Kelly
AU - Llatjós, Roger
AU - Blasco-Lucas, Arnau
AU - González Kuguel, Sebastián
AU - Sbraga, Fabrizio
AU - Galli, Cesare
AU - Padler-Karavani, Vered
AU - Le Tourneau, Thierry
AU - Vadori, Marta
AU - Roussel, Jean
AU - Bottio, Tomaso
AU - Cozzi, Emanuele
AU - Soulillou, Jean-Paul
AU - Galiñanes, Manuel
AU - Manez, Rafael
AU - Costa, Cristina
N1 - © 2025 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2025/12/31
Y1 - 2025/12/31
N2 - Structural valve deterioration (SVD) remains a key limitation in bioprosthetic heart valve (BHV) usage influenced by patient age. A deeper understanding of SVD pathogenesis, particularly of the immune-mediated processes altering current BHV materials, is therefore critical. To this end, commercially available BHV tissues of bovine, porcine, and equine origin were investigated following subcutaneous implantation into α1,3-galactosyltransferase-knockout (Gal KO) mice. We compared the immune responses between adult and aged animals via histological assessments of explants and measurement of serum anti-galactose α1,3-galactose (Gal) and anti-non-Gal antibodies at 2 months post-implantation. In contrast to adult mice, old Gal KO mice did not show increased levels of serum anti-Gal or -non-Gal antibodies after receiving specific BHV tissue (i.e., Freedom-Solo). Instead, a significant decrease in serum anti-Gal IgM was found in old recipients of Freedom-Solo. Furthermore, the overall cellular immune response was attenuated in explants from old mice compared with adults (i.e., ATS 3f and Crown). Nevertheless, the Freedom-Solo (bovine) and the Hancock-II (porcine) tissues still elicited strong cellular immune infiltration in the old cohorts. Therefore, the Gal KO mouse model offers a valuable platform to investigate age-related differences regarding cellular and humoral immune responses to various BHV tissues, contributing to our understanding of SVD.
AB - Structural valve deterioration (SVD) remains a key limitation in bioprosthetic heart valve (BHV) usage influenced by patient age. A deeper understanding of SVD pathogenesis, particularly of the immune-mediated processes altering current BHV materials, is therefore critical. To this end, commercially available BHV tissues of bovine, porcine, and equine origin were investigated following subcutaneous implantation into α1,3-galactosyltransferase-knockout (Gal KO) mice. We compared the immune responses between adult and aged animals via histological assessments of explants and measurement of serum anti-galactose α1,3-galactose (Gal) and anti-non-Gal antibodies at 2 months post-implantation. In contrast to adult mice, old Gal KO mice did not show increased levels of serum anti-Gal or -non-Gal antibodies after receiving specific BHV tissue (i.e., Freedom-Solo). Instead, a significant decrease in serum anti-Gal IgM was found in old recipients of Freedom-Solo. Furthermore, the overall cellular immune response was attenuated in explants from old mice compared with adults (i.e., ATS 3f and Crown). Nevertheless, the Freedom-Solo (bovine) and the Hancock-II (porcine) tissues still elicited strong cellular immune infiltration in the old cohorts. Therefore, the Gal KO mouse model offers a valuable platform to investigate age-related differences regarding cellular and humoral immune responses to various BHV tissues, contributing to our understanding of SVD.
KW - bioprosthetic heart valves
KW - structural valve deterioration
KW - aging
KW - α1,3-galactosyltransferase-knockout mice
KW - anti-Gal antibodies
KW - cellular immune response
UR - https://www.scopus.com/pages/publications/105029030845
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:001670811000001&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.3390/bioengineering13010053
DO - 10.3390/bioengineering13010053
M3 - Article
SN - 2306-5354
VL - 13
JO - Bioengineering
JF - Bioengineering
ER -