优化巴厘昔单抗在肝移植中的应用

IF 0.1 Q4 TRANSPLANTATION Transplant Research and Risk Management Pub Date : 2010-01-06 DOI:10.2147/TRRM.S4829
C. Ramirez, Adam Bozdin, A. Frank, W. Maley, C. Doria
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引用次数: 5

摘要

抗体诱导治疗还不是肝移植中标准免疫抑制方案的一部分。然而,近年来,抗体诱导治疗在原位肝移植(OLT)中的应用呈上升趋势,这主要是由于2002年终末期肝病模型(MELD)评分系统采用后,出现肾功能不全的OLT受者越来越多。Basiliximab是一种嵌合单克隆抗体,是OLT中最常用的诱导抗体。Basiliximab靶向活化t淋巴细胞中白细胞介素-2受体α链,抑制t淋巴细胞增殖,导致急性细胞排斥反应。Basiliximab(在OLT后第0天和第4天静脉给予两次20 mg剂量)具有极好的疗效和安全性。Basiliximab诱导也允许早期类固醇停药或避免,以及延迟引入和最小化钙调磷酸酶抑制剂(CNI)在肾功能不全的设置。尽管目前尚不清楚其对OLT后丙型肝炎病毒(HCV)复发的长期影响,但在无类固醇方案中使用巴吉昔单抗诱导的研究表明,对HCV的组织学复发和生存率没有有害影响。Basiliximab是一种耐受性良好、有效且安全的抗排斥药物,适用于儿童和成人OLT受者,与基于cni的免疫疗法联合使用。
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Optimizing use of basiliximab in liver transplantation
Antibody induction therapy has not been part of standard immunosuppressive regimens in liver transplantation. However, in recent years there has been an upward trend in the use of antibody induction therapy in orthotopic liver transplantation (OLT), attributed mainly to the growing number of OLT recipients with renal dysfunction after the Model for End Stage Liver Disease (MELD) scoring system was adopted in 2002. Basiliximab, a chimeric monoclonal antibody, is the most frequently used induction antibody in OLT. Basiliximab targets the alpha chain of interleukin-2 receptors in activated T-lymphocytes, inhibiting T-lymphocyte proliferation responsible for acute cellular rejection. Basiliximab (given in two 20 mg doses intravenously on post OLT day 0 and 4) has an excellent efficacy and safety profile. Basiliximab induction also allows early steroid withdrawal or avoidance, as well as delayed introduction and minimization of calcineurin inhibitors (CNI) in the setting of renal insufficiency. Although its long-term effect on hepatitis C virus (HCV) recurrence post OLT is currently unknown, studies using basiliximab induction in steroid-free protocols suggest no harmful effect on histologic HCV recurrence and survival rates. Basiliximab is a well tolerated, effective and safe anti-rejection drug in pediatric and adult OLT recipients when given in conjunction with a CNI-based immunotherapy.
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
6
审稿时长
16 weeks
期刊最新文献
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