1 Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan. 2 Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan. 3 Division of Surgery, Harasanshin Hospital, Fukuoka, Japan. 4 Department of Urology, Tokyo Women's Medical University, Tokyo, Japan. 5 Department of Integrated Therapy for Chronic Kidney Disease, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Transplantation. 2017 Jun;101(6):1416-1422. doi: 10.1097/TP.0000000000001324.
ABO-incompatible (ABO-I) kidney transplantation (KTx) is an established procedure to expand living donor sources. Although graft and patient survival rates are comparable between ABO-compatible (ABO-C) and ABO-I KTx, several studies have suggested that ABO-I KTx is associated with infection. Additionally, the histological findings and incidence of antibody-mediated rejection under desensitization with rituximab and plasmapheresis remain unclear.
We reviewed 327 patients who underwent living-donor KTx without preformed donor-specific antibodies (ABO-C, n = 226; ABO-I, n = 101). Patients who underwent ABO-I KTx received 200 mg/body of rituximab and plasmapheresis, and protocol biopsy (PB) was planned at 3 and 12 months. We compared the PB findings, cumulative incidence of acute rejection in both PBs and indication biopsies, infection, and patient and graft survivals.
The 3- and 12-month PBs were performed in 85.0% and 79.2% of the patients, respectively. Subclinical acute rejection occurred in 6.9% and 9.9% of patients in the ABO-C and ABO-I groups at 3 months (P = 0.4) and in 12.4% and 10.1% at 12 months, respectively (P = 0.5). The cumulative incidence of acute rejection determined by both PBs and indication biopsies was 20.5% and 19.6%, respectively (P = 0.8). The degrees of microvascular inflammation and interstitial fibrosis/tubular atrophy were comparable. Polyomavirus BK nephropathy was found in 2.7% and 3.0% of patients in the ABO-C and ABO-I groups, respectively (P = 1.0). The incidence of other infections and the graft/patient survival rates were not different.
Analyses using 3- and 12-month PBs suggested comparable allograft pathology between ABO-C and ABO-I KTx under desensitization with low-dose rituximab and plasmapheresis.
ABO 不相容(ABO-I)肾移植(KTx)是扩大活体供者来源的一种既定方法。尽管 ABO 相容(ABO-C)和 ABO-I KTx 之间的移植物和患者存活率相当,但几项研究表明,ABO-I KTx 与感染有关。此外,在使用利妥昔单抗和血浆置换进行脱敏治疗下,抗体介导的排斥反应的组织学发现和发生率尚不清楚。
我们回顾了 327 名接受无预先形成的供体特异性抗体的活体供者 KTx 的患者(ABO-C,n=226;ABO-I,n=101)。接受 ABO-I KTx 的患者接受了 200mg/体的利妥昔单抗和血浆置换,并计划在 3 个月和 12 个月进行方案活检(PB)。我们比较了 PB 结果、两次 PB 和指示活检的急性排斥反应累积发生率、感染以及患者和移植物存活率。
分别有 85.0%和 79.2%的患者进行了 3 个月和 12 个月的 PB。在 3 个月时,ABO-C 和 ABO-I 组的患者分别有 6.9%和 9.9%发生亚临床急性排斥反应(P=0.4),在 12 个月时分别有 12.4%和 10.1%发生亚临床急性排斥反应(P=0.5)。通过两次 PB 和指示活检确定的急性排斥反应累积发生率分别为 20.5%和 19.6%(P=0.8)。微血管炎症和间质纤维化/肾小管萎缩的程度相似。BK 多瘤病毒肾病分别在 ABO-C 和 ABO-I 组中发现了 2.7%和 3.0%的患者(P=1.0)。其他感染的发生率和移植物/患者存活率没有差异。
使用 3 个月和 12 个月的 PB 分析表明,在使用低剂量利妥昔单抗和血浆置换进行脱敏治疗下,ABO-C 和 ABO-I KTx 的同种异体移植物病理学相似。