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Synergistic effect of vincristine with tacrolimus or sirolimus in prevention of acute heart allograft rejection in the rat

✍ Scribed by Wenlei Jiang; Jingen Jiang; Dasheng Xu; Xiang Wang; Shijie Qi; Jun Ouyang; Anlun Ma; Minh Diem Vu; Kupa K. Bilolo; Huifang Chen


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
177 KB
Volume
23
Category
Article
ISSN
0738-1085

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✦ Synopsis


Abstract

The application of multiple immunosuppressive therapy for organ transplantation could enhance therapeutic efficacy, while minimizing the toxicity of individual drugs used in the regimen. In this study, the effect of the combined therapy of vincristine (VCR) with tacrolimus (FK506) or sirolimus (rapamycin, RAPA) was tested in prevention of acute heart allograft rejection in the rat. A Brown Norway (BN, RT 1^n^) to Lewis (LEW, RT 1^1^) rat combination was used in a heart allografting model. VCR was administered intraperitoneally once daily, while FK506 and RAPA were given by gavage once daily for 14 days after transplantation. There were dose‐related prolongations of mean survival time (MST) to monotherapy of VCR, FK506, or RAPA. The MST in combination therapy indicated that a synergistic interaction was produced when compared with the respective monotherapies: VCR 0.05 mg/kg/day + FK506 0.5 mg/kg/day (16.00 ± 1.79 days, P = 0.001; combination index (CI) = 0.557); VCR 0.05 mg/kg/day + FK506 1.0 mg/kg/day (29.00 ± 10.54 days, P = 0.001; CI = 0.598); VCR 0.05 mg/kg/day + RAPA 0.2 mg/kg/day (17.33 ± 1.97 days, P = 0.001; CI = 0.500); and VCR 0.05 mg/kg/day + RAPA 0.4 mg/kg/day (21.17 ± 3.19 days, P = 0.001; CI = 0.838). Combination therapy of VCR and FK506 or RAPA produced synergistic effects in prevention of acute heart allograft rejection in the rat. © 2003 Wiley‐Liss, Inc. MICROSURGERY 23:117–122 2003


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