Bhaskaran Madhu C, Heidt Sebastiaan, Muthukumar Thangamani
Division of Kidney Diseases and Hypertension, Department of Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Great Neck, New York, USA.
Kidney Transplant Program, Northwell Health, Manhasset, New York, USA.
Kidney Int Rep. 2022 Mar 15;7(6):1179-1188. doi: 10.1016/j.ekir.2022.03.006. eCollection 2022 Jun.
Human leukocyte antigens (HLAs) are the primary determinants of alloimmunity. A crossmatch test is a test that determines the immunologic risk of a recipient with a potential donor by ensuring that there are no transplant-relevant circulating antibodies in the recipient directed against donor antigens. Physical crossmatch (PXM) tests, such as complement-dependent cytotoxicity crossmatch (CDCXM) and flow cytometry crossmatch (FCXM), require mixing of patient serum and donor cells, are labor intensive, and are logistically challenging. Virtual crossmatch (VXM) test assesses immunologic compatibility between recipient and potential donor by analyzing the results of 2 independently done physical laboratory tests-patient anti-HLA antibody and donor HLA typing. The goal of VXM is pretransplant risk stratification-though there is no consensus on whether such risk assessment involves predicting the PXM result or the posttransplant outcome. Although the concept of VXM is not new, the advent of solid-phase assays for detecting circulating antibodies in the recipient directed against individual HLA and DNA-based methods for typing donor HLA specificities at a higher resolution makes the routine use of VXM a reality. Accordingly, VXM may be applied at different scenarios-both for sensitized and nonsensitized patients. Implementation of VXM-based approach has resulted in statistically significant reduction in cold ischemia time without an increase in hyperacute rejection episodes. Though there are considerable challenges, VXM is expected to be used more often in the future, depending on the transplant center's tolerance of immunologic risk.
人类白细胞抗原(HLA)是同种免疫的主要决定因素。交叉配型试验是一种通过确保受者体内不存在针对供者抗原的与移植相关的循环抗体,来确定潜在供者与受者之间免疫风险的试验。物理交叉配型(PXM)试验,如补体依赖细胞毒性交叉配型(CDCXM)和流式细胞术交叉配型(FCXM),需要将患者血清和供者细胞混合,劳动强度大,且在后勤方面具有挑战性。虚拟交叉配型(VXM)试验通过分析两项独立进行的物理实验室检测结果——患者抗HLA抗体和供者HLA分型,来评估受者与潜在供者之间的免疫相容性。VXM的目标是移植前风险分层——尽管对于这种风险评估是涉及预测PXM结果还是移植后结果尚无共识。虽然VXM的概念并不新鲜,但用于检测受者体内针对个体HLA的循环抗体的固相检测方法以及用于以更高分辨率对供者HLA特异性进行分型的基于DNA的方法的出现,使得VXM的常规应用成为现实。因此,VXM可应用于不同场景——无论是致敏患者还是非致敏患者。基于VXM方法的实施已使冷缺血时间在统计学上显著缩短,而超急性排斥反应发生率并未增加。尽管存在相当大的挑战,但根据移植中心对免疫风险的耐受性,预计VXM在未来会更频繁地使用。