Thibaudin D, Alamartine E, de Filippis J P, Diab N, Laurent B, Berthoux F
Service de Néphrologie Dialyse Transplantation Rénale, CHRU de Saint-Etienne, France.
Nephrol Dial Transplant. 1998 Mar;13(3):711-5. doi: 10.1093/ndt/13.3.711.
Sensitized kidney allograft recipients require special management to improve their outcome. One strategy is heavy immunosuppression with antilymphocyte antibodies. Controversy continues about the actual advantage of induction protocols whilst infections and cancers are a constant risk. In addition, little is known about how to handle sensitized patients with low levels of sensitization.
In this study, we randomized sensitized renal transplant recipients, who received prophylactic treatment with or without antithymocyte globulin (ATG), in addition to a standard triple regimen consisting of cyclosporin, steroids and azathioprine at ATG discontinuation. The induction treatment consisted of a low-dose ATG course over 10 days. Randomization was stratified on the maximum PRA, according to the five following classes: 5% < PRA < or = 20%, 20% < PRA < or = 40%, 40% < PRA < or = 60%, 60% < PRA < or = 80% and 80% < PRA < or = 100%.
Eighty nine patients were enrolled: 47 patients received ATG and 42 did not. ATG induction lowered the incidence of biopsy-proven acute rejection episodes from 64 to 38%, increased 1 year graft survival from 76 to 89% and was associated with a higher 1 year inulin clearance (37+/-15 vs 49+/-18 ml/min). ATG-associated side effects were restricted to leucopenia and thrombocytopenia, whereas bacterial and viral infections, gammopathies and cancers did not occur more frequently. ATG induction benefited all sensitized patients, and not only the hypersensitized patients.
We conclude that ATG induction is beneficial for all sensitized patients, regardless of their level of sensitization, with regard to acute rejection episodes, graft survival and graft function. Low-dose ATG is sufficient and prevents additional complications.
致敏肾移植受者需要特殊管理以改善其预后。一种策略是使用抗淋巴细胞抗体进行强化免疫抑制。关于诱导方案的实际优势仍存在争议,同时感染和癌症始终是风险。此外,对于如何处理低致敏水平的致敏患者知之甚少。
在本研究中,我们将致敏肾移植受者随机分组,除了在停用抗胸腺细胞球蛋白(ATG)时使用环孢素、类固醇和硫唑嘌呤组成的标准三联疗法外,一组接受或不接受ATG预防性治疗。诱导治疗包括为期10天的低剂量ATG疗程。根据最大群体反应性抗体(PRA),分为以下五类进行随机分层:5% < PRA ≤ 20%、20% < PRA ≤ 40%、40% < PRA ≤ 60%、60% < PRA ≤ 80% 和 80% < PRA ≤ 100%。
共纳入89例患者:47例接受ATG治疗,42例未接受。ATG诱导使活检证实的急性排斥反应发生率从64%降至38%,1年移植肾存活率从76%提高到89%,并且与1年菊粉清除率较高相关(37±15 vs 49±18 ml/min)。与ATG相关的副作用仅限于白细胞减少和血小板减少,而细菌和病毒感染、丙种球蛋白病和癌症并未更频繁发生。ATG诱导对所有致敏患者有益,而不仅是高度致敏患者。
我们得出结论,就急性排斥反应、移植肾存活和移植肾功能而言,ATG诱导对所有致敏患者有益,无论其致敏水平如何。低剂量ATG就足够了,并可预防额外并发症。