TY - JOUR
T1 - Sprayable proteinic adhesive microgel-based immunosuppressive therapeutic coating for effective xenograft transplantation
AU - Lee, Sangmin
AU - Woo, Hyun Tack
AU - Lee, Hyeokjun
AU - Choi, Geunho
AU - Joo, Kye Il
AU - Cha, Hyung Joon
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2026/1/10
Y1 - 2026/1/10
N2 - Tissue transplantation is an essential therapeutic approach for restoring function in patients with tissue damage caused by aging or accidents. However, immune rejection remains a significant challenge because the host immune system recognizes transplanted xenografts as foreign, triggering systemic inflammatory responses and graft failures. Although conventional oral or intravenous immunosuppressive therapies can mitigate immune rejection, they are often associated with severe systemic side effects and increased risk of infection. To address these challenges, a sprayable proteinic adhesive microgel (MG) coating system (Immune-shield) is developed using bioengineered mussel adhesive protein (MAP). Owing to its intrinsically disordered structure, MAPs exhibit low immune response, enabling localized and sustained delivery of immunosuppressive drugs. Immune-shield is directly applied to transplanted wet tissue surfaces using a simple spray and adheres strongly. It forms a stable coating that enables prolonged local retention and controlled release of cyclosporin A (CsA), a model immunosuppressive drug. In a rat skin xenograft model, Immune-shield effectively reduces inflammation and immune cell infiltration at the graft site, demonstrating effective local immunosuppressive efficacy without systemic drug administration. These results demonstrate the potential of sprayable, low-immunogenic protein-based adhesive MGs as a targeted immunosuppressive therapeutic platform for tissue and organ transplantation.
AB - Tissue transplantation is an essential therapeutic approach for restoring function in patients with tissue damage caused by aging or accidents. However, immune rejection remains a significant challenge because the host immune system recognizes transplanted xenografts as foreign, triggering systemic inflammatory responses and graft failures. Although conventional oral or intravenous immunosuppressive therapies can mitigate immune rejection, they are often associated with severe systemic side effects and increased risk of infection. To address these challenges, a sprayable proteinic adhesive microgel (MG) coating system (Immune-shield) is developed using bioengineered mussel adhesive protein (MAP). Owing to its intrinsically disordered structure, MAPs exhibit low immune response, enabling localized and sustained delivery of immunosuppressive drugs. Immune-shield is directly applied to transplanted wet tissue surfaces using a simple spray and adheres strongly. It forms a stable coating that enables prolonged local retention and controlled release of cyclosporin A (CsA), a model immunosuppressive drug. In a rat skin xenograft model, Immune-shield effectively reduces inflammation and immune cell infiltration at the graft site, demonstrating effective local immunosuppressive efficacy without systemic drug administration. These results demonstrate the potential of sprayable, low-immunogenic protein-based adhesive MGs as a targeted immunosuppressive therapeutic platform for tissue and organ transplantation.
KW - Immune suppression
KW - Mussel adhesive protein
KW - Sprayable adhesive microgel
KW - Surface coating
KW - Xenograft transplantation
UR - https://www.scopus.com/pages/publications/105024865776
U2 - 10.1016/j.jconrel.2025.114468
DO - 10.1016/j.jconrel.2025.114468
M3 - Article
C2 - 41308753
AN - SCOPUS:105024865776
SN - 0168-3659
VL - 389
JO - Journal of Controlled Release
JF - Journal of Controlled Release
M1 - 114468
ER -