Department of Transfusion Medicine, Histocompatibility and Molecular Biology, Jaypee Hospital, Noida, India.
Department of Nephrology and Renal Transplantation, Jaypee Hospital, Noida, India.
Ther Apher Dial. 2020 Oct;24(5):578-590. doi: 10.1111/1744-9987.13467. Epub 2020 Feb 11.
Successful renal transplantation across HLA barrier in sensitized individuals has been on the rise during the past decade, primarily due to improved desensitization regimes. The aim of this study was to share outcome of desensitization in renal transplant recipients with donor-specific anti-HLA antibodies (DSA). This was a retrospective analysis of all HLA immunized individuals who were prospective renal transplant recipients. All such patients underwent preconditioning as per the institutional desensitization protocol. Complement-dependent cytoxicity-based crossmatch (CDC-XM), luminex-based crossmatch (LM-XM) and flowcytometry-based crossmatch (FC-XM) were done in all cases. If any of these tests turned out positive, single antigen bead assay (SAB) was performed. Desensitization for DSA was performed in 55 patients and all patients were followed-up for 1 year to assess graft function and patient outcome. CDC-XM being a less sensitive assay, could not detect incompatibility in 29 (52.73%) cases. After desensitization, even though SAB and LM-XM results revealed an MFI within acceptable range, FC-XM being an extremely sensitive assay, continued to give a positive result in eight (14.55%) cases. The mean ± SD number of pretransplant TPE were 3.44 ± 0.98 (2-11). Out of 55, there were 10 patients who were lost to follow up. Patient and graft survival of 45 patients at 1 year was found to be 100%. Preconditioning for renal transplants in the form of immunosuppression with TPE is an extremely useful auxiliary for transplantation in HLA sensitized renal transplant recipients.
在过去十年中,由于脱敏方案的改进,HLA 屏障跨器官移植在致敏个体中的成功率一直在上升。本研究旨在分享具有供体特异性抗 HLA 抗体 (DSA) 的肾移植受者脱敏的结果。这是对所有前瞻性肾移植受者进行 HLA 免疫的个体的回顾性分析。所有此类患者均根据机构脱敏方案进行预处理。所有情况下均进行基于补体依赖性细胞毒性的交叉配型 (CDC-XM)、基于 Luminex 的交叉配型 (LM-XM) 和基于流式细胞术的交叉配型 (FC-XM)。如果这些测试中的任何一项呈阳性,则进行单抗原珠测定 (SAB)。对 55 例 DSA 进行脱敏,所有患者均随访 1 年,以评估移植物功能和患者结局。CDC-XM 作为一种敏感性较低的检测方法,无法检测出 29 例(52.73%)患者的不兼容情况。脱敏后,即使 SAB 和 LM-XM 结果显示 MFI 在可接受范围内,FC-XM 作为一种极其敏感的检测方法,在 8 例(14.55%)患者中仍持续呈阳性结果。移植前 TPE 的平均 ± SD 数量为 3.44 ± 0.98(2-11)。在 55 例中,有 10 例患者失访。45 例患者在 1 年内的患者和移植物存活率为 100%。以 TPE 形式进行免疫抑制预处理的肾移植是 HLA 致敏肾移植受者移植的一种非常有用的辅助手段。