2026-04-14T10:21:14Z
2026-04-14T10:21:14Z
2025-12-31
2026-02-24T12:34:34Z
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 alpha 1,3-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 alpha 1,3-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.
Article
Published version
English
Immunologia de la trasplantació; Malalties del cor; Vàlvules cardíaques; Transplantation immunology; Heart diseases; Heart valves
MDPI AG
Reproducció del document publicat a: https://doi.org/10.3390/bioengineering13010053
Bioengineering, 2025, vol. 13, issue. 1, p. 53
https://doi.org/10.3390/bioengineering13010053
cc-by (c) Casós, Kelly et al. 2025
https://creativecommons.org/licenses/by/4.0/