Experience with daclizumab in liver transplantation - Renal transplant dosing without calcineurin inhibitors is insufficient to prevent acute rejection in liver transplantation

被引:63
作者
Hirose, R
Roberts, JP
Quan, D
Osorio, RW
Freise, C
Ascher, NL
Stock, PG
机构
[1] Univ Calif San Francisco, Div Transplantat, Dept Surg, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Pharm, San Francisco, CA 94143 USA
[3] Calif Pacific Med Ctr, Dept Surg, San Francisco, CA 94115 USA
关键词
D O I
10.1097/00007890-200001270-00019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Daclizumab is a monoclonal antibody directed against the cu chain of the interleukin 2 receptor. We review our experience with the use of daclizumab in liver transplant recipients. Methods. Thirty-two patients were given daclizumab as induction therapy in the setting of hepatic transplantation. Seven of these patients were enrolled in a pilot study to determine the efficacy of daclizumab in conjunction with corticosteroids and mycophenolate mofetil without the initial use of calcineurin inhibitors (CI). The remaining 25 patients received daclizumab, mycophenolate mofetil, and steroids, with the institution of CI generally within the first postoperative week. The majority of these patients (n=17) had some degree of renal insufficiency. Results, The pilot study was halted after the first seven patients were enrolled because of an unacceptably high rate of rejection (7/7=100%). The patients outside of this pilot study, however, had a much lower rate of rejection (36%). The incidence and severity of rejection correlated with the delay in institution of CI. The described dosing schedule resulted in subtherapeutic daclizumab levels in liver transplant recipients, Conclusions. Daclizumab used in liver transplant recipients without any CI was ineffective and can potentially lead to steroid-resistant rejection, The dosing regimen used in renal transplant recipients is most likely insufficient for liver transplant patients. However, daclizumab can be used safely in patients with preexisting or postoperative renal dysfunction in conjunction with low doses of CI given within the first week postoperatively.
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收藏
页码:307 / 311
页数:5
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