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人白细胞抗原(HLA)匹配的活体供肾移植中霉酚酸酯的长期单药治疗

Long-term mycophenolate monotherapy in human leukocyte antigen (HLA)-identical living-donor kidney transplantation.

作者信息

Gascó Blanca, Revuelta Ignacio, Sánchez-Escuredo Ana, Blasco Miquel, Cofán Federico, Esforzado Nuria, Quintana Luis F, Ricart María José, Torregrosa José Vicente, Campistol Josep M, Oppenheimer Federico, Diekmann Fritz

机构信息

Servicio de Nefrología y Trasplante Renal, Hospital Clínic, Villarroel 170 08036 Barcelona, Spain.

出版信息

Transplant Res. 2014 Feb 3;3(1):4. doi: 10.1186/2047-1440-3-4.

Abstract

UNLABELLED

Although recipients of a first HLA-identical living-donor kidney transplant seem to need less immunosuppression, there are no guideline recommendations for these patients, and few prospective trials are available.

METHODS

We analyzed all PRA-negative patients who received a first kidney transplant from an HLA-identical living donor. The patients received no antibody induction. An intraoperative bolus of 500 mg of methylprednisolone was administered. Then, steroid therapy was withdrawn within one week. Tacrolimus and mycophenolate treatment were started 3 days before transplantation with tacrolimus target levels of 4 to 8 ng/mL. In the absence of rejection, tacrolimus was withdrawn between 3 and 12 months post-transplant to reach mycophenolate mofetil monotherapy of 2 g/day or equivalent.

RESULTS

Six patients were treated with the above protocol. At last follow-up, graft and patient survival were 100%. MDRD glomerular filtration rates were 54, 60, and 62 mL/min at 3 months, 12 months and last follow-up, respectively. None of the patients developed PRA post-transplant. One episode of acute rejection Banff IA occurred 9 years after transplantation due to non-adherence with good outcome after treatment. The mean number of concomitant drugs given with mycophenolate was 2.6. Four patients needed antihypertensive drugs.

CONCLUSION

Steroid-free de novo treatment and calcineurin-inhibitor weaning with mycophenolate monotherapy is feasible in first HLA-identical kidney transplantation from a living sibling.

摘要

未标注

尽管首次接受 HLA 完全相同的活体供肾移植的受者似乎需要较少的免疫抑制,但对于这些患者尚无指南推荐,且前瞻性试验也很少。

方法

我们分析了所有接受来自 HLA 完全相同的活体供者的首次肾移植且 PRA 阴性的患者。患者未接受抗体诱导治疗。术中给予 500 毫克甲泼尼龙静脉推注。然后,在一周内停用类固醇治疗。在移植前 3 天开始使用他克莫司和霉酚酸酯治疗,他克莫司目标血药浓度为 4 至 8 纳克/毫升。在无排斥反应的情况下,移植后 3 至 12 个月停用他克莫司,以达到霉酚酸酯单药治疗剂量为 2 克/天或等效剂量。

结果

6 例患者采用上述方案治疗。在最后一次随访时,移植肾和患者生存率均为 100%。3 个月、12 个月及最后一次随访时的 MDRD 肾小球滤过率分别为 54、60 和 62 毫升/分钟。所有患者移植后均未出现 PRA。1 例患者在移植 9 年后因不依从发生 1 次急性排斥反应(Banff IA 级),治疗后预后良好。与霉酚酸酯联合使用的伴随药物平均数量为 2.6 种。4 例患者需要服用降压药。

结论

在首次接受来自同胞活体的 HLA 完全相同的肾移植中,无类固醇的初始治疗及用霉酚酸酯单药治疗逐渐停用钙调神经磷酸酶抑制剂是可行的。

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