Division of Nephrology and Hypertension and Transplant Center, Department of Internal Medicine, Mayo Clinic and Foundation, 200 First Street SW, Rochester, MN 55905, USA.
Am J Transplant. 2010 Mar;10(3):582-9. doi: 10.1111/j.1600-6143.2009.02985.x. Epub 2010 Jan 29.
Renal transplant candidates with donor-specific alloantibody (DSA) have increased risk of antibody-mediated allograft injury. The goal of this study was to correlate the risk of antibody-mediated rejection (AMR), transplant glomerulopathy (TG) and graft survival with the baseline DSA level (prior to initiation of pretransplant conditioning). These analyses include 119 positive crossmatch (+XM) compared to 70 negative crossmatch (-XM) transplants performed between April 2000 and July 2007. Using a combination of cell-based crossmatch tests, DSA level was stratified into very high +XM, high +XM, low +XM and -XM groups. In +XM transplants, increasing DSA level was associated with increased risk for AMR (HR = 1.76 [1.51, 2.07], p = 0.0001) but not TG (p = 0.18). We found an increased risk for both early and late allograft loss associated with very high DSA (HR = 7.71 [2.95, 20.1], p = 0.0001). Although lower DSA recipients commonly developed AMR and TG, allograft survival was similar to that of -XM patients (p = 0.31). We conclude that the baseline DSA level correlates with risk of early and late alloantibody-mediated allograft injury. With current protocols, very high baseline DSA patients have high rates of AMR and poor long-term allograft survival highlighting the need for improved therapy for these candidates.
肾移植受者携带供体特异性抗体(DSA)会增加抗体介导的移植物损伤风险。本研究旨在探讨基线 DSA 水平(移植前预处理前)与抗体介导排斥反应(AMR)、移植肾小球病(TG)和移植物存活率的相关性。这些分析包括 119 例阳性交叉配型(+XM)与 70 例阴性交叉配型(-XM)移植的比较,这些移植于 2000 年 4 月至 2007 年 7 月期间进行。使用细胞交叉配型检测的组合,将 DSA 水平分层为极高+XM、高+XM、低+XM 和 -XM 组。在+XM 移植中,DSA 水平的升高与 AMR 风险的增加相关(HR = 1.76 [1.51, 2.07],p = 0.0001),但与 TG 无关(p = 0.18)。我们发现,与极高 DSA 相关的早期和晚期移植物丢失风险均增加(HR = 7.71 [2.95, 20.1],p = 0.0001)。尽管低 DSA 受者常发生 AMR 和 TG,但移植物存活率与 -XM 患者相似(p = 0.31)。我们得出结论,基线 DSA 水平与早期和晚期同种异体抗体介导的移植物损伤风险相关。根据当前的方案,极高基线 DSA 患者 AMR 发生率高,长期移植物存活率差,突出了需要为这些患者提供更好的治疗方法。