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Antibody induction therapy in adult kidney transplantation: A controversy continues

机译:成人肾脏移植中的抗体诱导治疗:争议仍在

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摘要

Antibody induction therapy is frequently used as an adjunct to the maintenance immunosuppression in adult kidney transplant recipients. Published data support antibody induction in patients with immunologic risk to reduce the incidence of acute rejection (AR) and graft loss from rejection. However, the choice of antibody remains controversial as the clinical studies were carried out on patients of different immunologic risk and in the context of varying maintenance regimens. Antibody selection should be guided by a comprehensive assessment of immunologic risk, patient comorbidities, financial burden as well as the maintenance immunosuppressives. Lymphocyte-depleting antibody (thymoglobulin, ATGAM or alemtuzumab) is usually recommended for those with high risk of rejection, although it increases the risk of infection and malignancy. For low risk patients, interleukin-2 receptor antibody (basiliximab or daclizumab) reduces the incidence of AR without much adverse effects, making its balance favorable in most patients. It should also be used in the high risk patients with other medical comorbidities that preclude usage of lymphocyte-depleting antibody safely. There are many patients with very low risk, who may be induced with intravenous steroids without any antibody, as long as combined potent immunosuppressives are kept as maintenance. In these patients, benefits with antibody induction may be too small to outweigh its adverse effects and financial cost. Rituximab can be used in desensitization protocols for ABO and/or HLA incompatible transplants. There are emerging data suggesting that alemtuzumab induction be more successful than other antibody for promoting less intensive maintenance protocols, such as steroid withdrawal, tacrolimus monotherapy or lower doses of tacrolimus and mycophenolic acid. However, the long-term efficacy and safety of these unconventional strategies remains unknown.
机译:成年肾移植受者经常使用抗体诱导疗法作为维持免疫抑制的辅助手段。已发表的数据支持在具有免疫学风险的患者中诱导抗体,以减少急性排斥反应(AR)的发生率和因排斥反应而造成的移植物损失。然而,抗体的选择仍存在争议,因为针对具有不同免疫风险的患者以及在不同维持方案的情况下进行了临床研究。抗体的选择应以对免疫学风险,患者合并症,经济负担以及维持免疫抑制剂的全面评估为指导。虽然排斥反应抗体会增加感染和恶性肿瘤的风险,但通常建议排斥反应高的人使用淋巴细胞消耗抗体(胸腺球蛋白,ATGAM或阿来珠单抗)。对于低危患者,白细胞介素2受体抗体(basiliximab或daclizumab)可降低AR的发生率,而不会产生太多不良影响,从而使大多数患者的平衡变得有利。它也应用于患有其他合并症的高危患者,以免安全使用消耗淋巴细胞的抗体。许多风险很低的患者,只要保持联合有效的免疫抑制剂作为维持治疗,就可以用无任何抗体的静脉类固醇诱导。在这些患者中,抗体诱导的益处可能太小而无法抵消其不利影响和财务成本。利妥昔单抗可用于ABO和/或HLA不相容移植的脱敏方案中。有新的数据表明,阿仑单抗的诱导比其他抗体更能成功地促进强度较低的维持方案,例如类固醇戒断,他克莫司单药治疗或更低剂量的他克莫司和霉酚酸。但是,这些非常规策略的长期疗效和安全性仍然未知。

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