Erasmus Medical Center Transplant Institute, Department of Internal Medicine, University Medical Center Rotterdam, Rotterdam, Netherlands.
HLA Laboratory, Department of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Front Immunol. 2023 Jan 10;13:1093359. doi: 10.3389/fimmu.2022.1093359. eCollection 2022.
The impact of donor-specific antibodies (DSA) in (highly-) immunized living donor kidney transplant recipients is reported differentially in various patient cohorts.
We have performed a retrospective analysis of all consecutive HLA-incompatible living donor kidney transplant recipients in our center between 2010-2019. Recipients who underwent plasmafiltration for a positive CDC-crossmatch were excluded. For each DSA+ recipient (DSA+), one immunized recipient without DSA (pPRA+) and two non-immunized recipients (pPRA-) were included. Patient and graft survival were analyzed and a subgroup analysis of DSA+ recipients was performed.
For 63 DSA+ recipients, 63 PRA+ and 126 PRA- recipients were included. 26 (41%) had class I, 24 (38%) class II and 13 (21%) combined HLA class I and II DSA. Death-censored graft survival was inferior in DSA+ recipients compared to pPRA+ (HR 2.38 [95% CI 1.00-5.70]) as well as to pPRA- (HR 3.91 [1.86-8.22]). In multivariate analysis, DSA remained of negative influence on death-censored graft survival. Flowcytometric crossmatch, MFI value, HLA class and origin of DSA were not of significant impact.
In our cohort of (highly-) immunized recipients, pretransplant DSA led to inferior death-censored graft survival. There were no "safe" DSA characteristics since only DSA impacted death-censored graft survival.
供体特异性抗体(DSA)在(高度)免疫的活体供肾移植受者中的影响在不同的患者队列中报告结果不同。
我们对 2010-2019 年期间在我们中心进行的所有连续 HLA 不相容的活体供肾移植受者进行了回顾性分析。排除因 CDC 交叉配型阳性而行血浆滤过的受者。对于每个 DSA+受者(DSA+),我们纳入了一名无 DSA 的免疫受者(pPRA+)和两名非免疫受者(pPRA-)。分析患者和移植物存活率,并对 DSA+受者进行亚组分析。
在 63 名 DSA+受者中,纳入了 63 名 pPRA+和 126 名 pPRA-受者。26 名(41%)存在 I 类 HLA 抗体,24 名(38%)存在 II 类 HLA 抗体,13 名(21%)存在 I 类和 II 类 HLA 抗体的混合抗体。与 pPRA+(HR 2.38[95%CI 1.00-5.70])和 pPRA-(HR 3.91[1.86-8.22])相比,DSA+受者的无死亡原因移植物存活率较低。在多变量分析中,DSA 仍然对无死亡原因移植物存活率有负面影响。流式细胞交叉配型、MFI 值、HLA 类别和 DSA 的来源均无显著影响。
在我们的(高度)免疫受者队列中,移植前 DSA 导致无死亡原因移植物存活率降低。由于只有 DSA 影响无死亡原因移植物存活率,因此没有“安全”的 DSA 特征。