Lee Juhan, Park Borae G, Jeong Hyang Sook, Park Youn Hee, Kim Sinyoung, Kim Beom Seok, Kim Hye Jin, Huh Kyu Ha, Jeong Hyeon Joo, Kim Yu Seun
Department of Transplantation Surgery, Severance Hospital, Yonsei University Health System Department of Laboratory Medicine, Severance Hospital, Yonsei University Health System Department of Pathology, Severance Hospital, Yonsei University Health System Department of Nephrology, Severance Hospital, Yonsei University Health System Department of Surgery, Yonsei University College of Medicine, Seoul, Republic of Korea.
Medicine (Baltimore). 2017 Sep;96(39):e8145. doi: 10.1097/MD.0000000000008145.
Human leukocyte antigen (HLA) is the major immunologic barrier in kidney transplantation (KT). Various desensitization protocols to overcome the HLA barrier have increased the opportunity for transplantation in sensitized patients. In addition, technological advances in solid-phase assays have permitted more comprehensive assessment of donor-specific antibodies. Although various desensitization therapies and immunologic techniques have been developed, the final transplantation decision is still based on the classic complement-dependent cytotoxicity (CDC) crossmatch (XM) technique. Some patients who fail to achieve negative XM have lost their transplant opportunities, even after receiving sufficient desensitization therapies.
A 57-year-old male with end-stage renal disease secondary to chronic glomerulonephritis was scheduled to have a second transplant from his son, but CDC XM was positive.
Initial CDC XM (Initial T-AHG 1:32) and flow-cytometry XM were positive. Anti-HLA-B59 donor specific antibody was detected by Luminex single antigen assay.
Herein, we report a successful case of KT across a positive CDC XM (T-AHG 1:8 at the time of transplantation) by using C1q assay-directed, bortezomib-assisted desensitization. After confirming a negative conversion in the C1q donor-specific antibody, we decided to perform KT accepting a positive AHG-CDC XM of 1:8 at the time of transplantation.
The posttransplant course was uneventful and a protocol biopsy at 3 months showed no evidence of rejection. The patient had excellent graft function at 12 months posttransplant.
The results of XM test and solid-phase assay should be interpreted in the context of the individual patient.
人类白细胞抗原(HLA)是肾移植(KT)中的主要免疫屏障。各种克服HLA屏障的脱敏方案增加了致敏患者的移植机会。此外,固相检测技术的进步使得对供体特异性抗体的评估更加全面。尽管已经开发了各种脱敏疗法和免疫技术,但最终的移植决策仍然基于经典的补体依赖细胞毒性(CDC)交叉配型(XM)技术。一些未能实现XM阴性的患者即使接受了充分的脱敏治疗,也失去了移植机会。
一名57岁男性,因慢性肾小球肾炎继发终末期肾病,计划接受来自其儿子的第二次移植,但CDC XM呈阳性。
初始CDC XM(初始T - AHG 1:32)和流式细胞术XM均为阳性。通过Luminex单抗原检测法检测到抗HLA - B59供体特异性抗体。
在此,我们报告一例通过使用C1q检测指导、硼替佐米辅助脱敏成功进行的KT病例,该病例的CDC XM为阳性(移植时T - AHG 1:8)。在确认C1q供体特异性抗体转为阴性后,我们决定进行KT,接受移植时AHG - CDC XM为1:8的阳性结果。
移植后过程顺利,3个月时的方案活检未显示排斥反应迹象。患者在移植后12个月时移植肾功能良好。
XM检测和固相检测的结果应结合个体患者情况进行解读。