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Risk stratification by the virtual crossmatch : a prospective study in 233 renal transplantations

机译:虚拟交叉匹配的风险分层:233例肾移植的前瞻性研究

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摘要

The virtual crossmatch (virtual-XM) has been proposed for accurate identification of donor-specific HLA-antibodies, but large prospective studies assessing its value for pretransplant risk stratification are lacking. A total of 233 consecutive renal allograft recipients were prospectively stratified according to the virtual-XM. In patients with a negative virtual-XM (n=190, 82%), prospective cytotoxicity crossmatches (CDC-XM) were omitted, and they received standard immunosuppression. Virtual-XM positive patients were only transplanted if CDC-XM were negative. They received additional induction with anti-T-lymphocyte-globulin and intravenous immunoglobulins (n=43, 18%). The cumulative incidence of clinical/subclinical antibody-mediated rejection (AMR) at 1 year was lower in the negative virtual-XM than in the positive virtual-XM group [15/190 (8%) vs. 18/43 (42%); P>0.0001]. After a median follow-up of 2.6 years, allograft loss because of AMR occurred less often in the negative virtual-XM group (1% vs. 7%; P=0.04) and death-censored allograft survival at 2 years was higher (98% vs. 91%; P=0.02). Serum creatinine was not different at the last follow-up (129 ?m vs. 130 ?m; P=0.58). We conclude that a negative virtual-XM defines patients at low risk for AMR and early allograft loss, while a positive virtual-XM represents a significant risk for AMR despite enhanced induction therapy. This supports the utility of the virtual-XM for risk stratification and treatment allocation.
机译:已提出使用虚拟交叉匹配(virtual-XM)来准确鉴定供体特异性HLA抗体,但尚缺乏评估其在移植前风险分层中的价值的大型前瞻性研究。根据虚拟XM,总共对233位连续的同种异体肾移植受者进行了前瞻性分层。在虚拟XM阴性(n = 190,82%)的患者中,省略了预期的细胞毒性交叉匹配(CDC-XM),并且接受了标准的免疫抑制。仅当CDC-XM阴性时,才将Virtual-XM阳性患者移植。他们接受了抗T淋巴细胞球蛋白和静脉内免疫球蛋白的额外诱导(n = 43,18%)。阴性虚拟XM组在1年时临床/亚临床抗体介导的排斥反应(AMR)的累积发生率低于阳性虚拟XM组[15/190(8%)对18/43(42%) ; P> 0.0001]。中位随访2.6年后,虚拟XM阴性组中因AMR引起的同种异体移植损失较少发生(1%vs. 7%; P = 0.04),以死亡为条件的同种异体移植2年生存率更高(98) %对91%; P = 0.02)。末次随访时血清肌酐无差异(129μmvs. 130μm; P = 0.58)。我们得出的结论是,虚拟XM阴性定义为具有较低的AMR和早期同种异体移植风险的患者,而虚拟XM阳性表示尽管进行了增强的诱导治疗,但仍代表AMR的重大风险。这支持了虚拟XM用于风险分层和治疗分配的实用程序。

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