Fernández Constantino, Calvo María, Leite Natacha, López Andrés, Ferreiro Tamara, Ribera Roi, Seijo Rocío, Alonso Ángel
Servicio de Nefrología, Complexo Hospitalario Universitario A Coruña, La Coruña, España.
Servicio de Nefrología, Complexo Hospitalario Universitario A Coruña, La Coruña, España.
Nefrologia. 2017 Nov-Dec;37(6):638-645. doi: 10.1016/j.nefro.2017.06.006. Epub 2017 Jul 19.
Desensitisation is a procedure undergone by the recipient of a kidney transplant from a donor who is cross-match positive. The aim of this study was to present the outcomes from our hospital of kidney transplant recipients from HLA-incompatible live donors after desensitisation. We studied 32 patients aged 46±14 years with a mean fluorescence intensity (MFI) versus class I HLA of 7979±4089 and 6825±4182 MFI versus class II and relative intensity scale (RIS) of 8.9±7.6. The complement-dependent cytotoxicity (CDC) cross-matching test was positive in 18 patients, flow cytometry was positive in 7 patients and donor-specific antibodies (DEA) were detected in 7. The protocol used was rituximab, plasmapheresis/immunoadsorption, immunoglobulins, tacrolimus, mycophenolic acid derivatives and prednisone. After 8±3 sessions of plasmapheresis/immunoadsorption, 23 patients were trasplanted (71.9%) and desensitisation was ineffective in 9. There were baseline differences in MFI class I (P<.001), RIS (P=.008), and CDC cross-matching, DSA and flow cytometry (P=.05). MFI class I and RIS were predictors of inefficiency in ROC curves. After follow-up of 43±30 months, 13 patients (56%) presented postoperative bleeding, 3 (13%) delayed graft function, 4 (17.4%) acute rejection, 6 (26%) CMV viraemia and 1 (4%) BK viraemia. Five-year patient survival was 90%, with 86% allograft survival. Five-year creatinine was 1.5±0.4 and proteinuria was 0.5±0.7.
Kidney transplantation from HLA-incompatible live donors after desensitisation was possible in 71.9% of patients. MFI class I and RIS predict the inefficiency of desensitisation. Five-year allograft survival (86%) was acceptable with a low incidence of acute rejection (17.4%), although with a greater trend towards postoperative bleeding.
脱敏是肾移植受者接受来自交叉配型阳性供体的肾脏移植时所经历的一种程序。本研究的目的是呈现我院经脱敏后接受来自HLA不相合活体供肾移植受者的结局。我们研究了32例年龄为46±14岁的患者,其与I类HLA的平均荧光强度(MFI)为7979±4089,与II类HLA的MFI为6825±4182,相对强度标度(RIS)为8.9±7.6。18例患者补体依赖细胞毒性(CDC)交叉配型试验呈阳性,7例患者流式细胞术呈阳性,7例检测到供体特异性抗体(DEA)。所采用的方案为利妥昔单抗、血浆置换/免疫吸附、免疫球蛋白、他克莫司、霉酚酸衍生物和泼尼松。经过8±3次血浆置换/免疫吸附治疗后,23例患者接受了移植(71.9%),9例脱敏治疗无效。I类MFI、RIS以及CDC交叉配型、供体特异性抗体和流式细胞术存在基线差异(P<0.001、P = 0.008、P = 0.05)。I类MFI和RIS在ROC曲线中是脱敏无效的预测指标。随访43±30个月后,13例患者(56%)出现术后出血,3例(13%)发生移植肾功能延迟,4例(17.4%)发生急性排斥反应,6例(26%)发生巨细胞病毒血症,1例(4%)发生BK病毒血症。患者5年生存率为90%,移植肾5年生存率为86%。5年时血肌酐为1.5±0.4,蛋白尿为0.5±0.7。
经脱敏后,71.9%的患者能够接受来自HLA不相合活体供肾的移植。I类MFI和RIS可预测脱敏治疗的无效性。移植肾5年生存率(86%)可接受,急性排斥反应发生率较低(17.4%),尽管术后出血趋势更明显。