Bakr Mohamed Adel, Nagib Ayman Maher, Donia Ahmed Farouk
Urology Nephrology Center, Mansoura University, Mansoura, Egypt.
Exp Clin Transplant. 2014 Mar;12 Suppl 1:60-9. doi: 10.6002/ect.25liver.l58.
Induction therapy after kidney transplantation is intensive immunosuppression in the initial days after transplant when the immune system of the recipient has the first contact with donor antigens. Initial intensive immunosuppression may be required to prevent acute rejection and graft loss, and subsequent immunosuppression may be decreased to minimize adverse events associated with immunosuppressive drugs. Induction agents include lymphocyte-depleting antibodies such as rabbit antithymocyte globulin, alemtuzumab, muromonab-CD3, rituximab, and bortezomib; lymphocyte-nondepleting antibodies such as interleukin 2 receptor antibodies; and other discontinued or investigational agents such as efalizumab and alefacept. Induction therapy may be adjusted for special situations such as living-donor kidney transplant, pediatric transplant, hepatitis C virus-seropositive recipients, recipients who require desensitization, patients who are at risk for developing delayed graft function, and old donors. The optimal immunosuppressive regimen may vary, and clinical practice guidelines are available.
肾移植后的诱导治疗是在移植后的最初几天进行的强化免疫抑制,此时受者的免疫系统首次接触供体抗原。可能需要进行初始强化免疫抑制以预防急性排斥反应和移植物丢失,随后可减少免疫抑制以尽量减少与免疫抑制药物相关的不良事件。诱导药物包括淋巴细胞清除抗体,如兔抗胸腺细胞球蛋白、阿仑单抗、莫罗单抗-CD3、利妥昔单抗和硼替佐米;淋巴细胞非清除抗体,如白细胞介素2受体抗体;以及其他已停用或正在研究的药物,如依法利珠单抗和阿法赛特。对于特殊情况,如活体供肾移植、儿科移植、丙型肝炎病毒血清学阳性受者、需要脱敏的受者、有发生移植肾功能延迟风险的患者以及老年供者,诱导治疗可进行调整。最佳免疫抑制方案可能有所不同,并且有临床实践指南可供参考。