TY - JOUR
T1 - The role of cyclosporin in prolonging survival in vascularized bone allografts
AU - Paskert, James P.
AU - Yaremchuk, Michael J.
AU - Randolph, Mark A.
AU - Weiland, Andrew J.
PY - 1987/8
Y1 - 1987/8
N2 - It is known that experimental vascularized bone allo-grafts are subject to host rejection. To be useful clinically, this rejection response would need to be controlled. Cyclosporin is a potent immunosuppressant whose precise role in vascularized bone allograft transplantation has not been established. Using a proven reliable vascularized knee allograft model in inbred rats, cyclosporin was used postoperatively both continuously and short term (14 days after transplant) at 10 mg/kg per day as recipient treatment. Across a strong histocompatibility barrier, continuous cyclosporin was required for long-term graft survival. Short-term therapy delayed rejection for 4 to 6 weeks. However, across a weak histocompatibility barrier, short-term therapy was as effective as continuous therapy in achieving long-term graft survival. The implication is that a limited course of cyclosporin may be clinically successful in sustaining vascularized bone allograft survival, provided the genetic disparity between graft and host has been minimized by genetic matching techniques.
AB - It is known that experimental vascularized bone allo-grafts are subject to host rejection. To be useful clinically, this rejection response would need to be controlled. Cyclosporin is a potent immunosuppressant whose precise role in vascularized bone allograft transplantation has not been established. Using a proven reliable vascularized knee allograft model in inbred rats, cyclosporin was used postoperatively both continuously and short term (14 days after transplant) at 10 mg/kg per day as recipient treatment. Across a strong histocompatibility barrier, continuous cyclosporin was required for long-term graft survival. Short-term therapy delayed rejection for 4 to 6 weeks. However, across a weak histocompatibility barrier, short-term therapy was as effective as continuous therapy in achieving long-term graft survival. The implication is that a limited course of cyclosporin may be clinically successful in sustaining vascularized bone allograft survival, provided the genetic disparity between graft and host has been minimized by genetic matching techniques.
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U2 - 10.1097/00006534-198708000-00014
DO - 10.1097/00006534-198708000-00014
M3 - Article
C2 - 3299419
AN - SCOPUS:0023640006
SN - 0032-1052
VL - 80
SP - 240
EP - 247
JO - Plastic and reconstructive surgery
JF - Plastic and reconstructive surgery
IS - 2
ER -