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Antibody and Cellular Immune Responses in Old α1,3-Galactosyltransferase-Knockout Mice Implanted with Bioprosthetic Heart Valve Tissues

  • Kelly Casós*
  • , Roger Llatjós
  • , Arnau Blasco-Lucas
  • , Sebastián González Kuguel
  • , Fabrizio Sbraga
  • , Cesare Galli
  • , Vered Padler-Karavani
  • , Thierry Le Tourneau
  • , Marta Vadori
  • , Jean Roussel
  • , Tomaso Bottio
  • , Emanuele Cozzi
  • , Jean-Paul Soulillou
  • , Manuel Galiñanes
  • , Rafael Manez
  • , Cristina Costa*
  • *Autor/a de correspondencia de este trabajo

Producción científica: Artículo en revista indizada › Artículo › revisión exhaustiva

1 Cita (Scopus)

Resumen

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.
Idioma originalInglés
Número de páginas17
PublicaciónBioengineering
Volumen13
DOI
EstadoPublicada - 31 dic 2025

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