Sengul Sule, Keven Kenan, Gormez Ulku, Kutlay Sim, Erturk Sehsuvar, Erbay Bulent
Department of Nephrology, Ankara University School of Medicine, Ankara, Turkey.
Transplantation. 2006 Apr 27;81(8):1216-9. doi: 10.1097/01.tp.0000203324.49969.30.
In this study, we investigated the impact of pre- and posttransplantation sCD30 monitoring on early (<6 months) acute rejection (AR) risk and analyzed the effect of different immunosuppressive regimens on posttransplantation sCD30 levels in kidney recipients. Fifty patients receiving kidney allograft and 10 healthy donors were included in this retrospective cohort study. Eight patients developed biopsy-proven AR (19%). In pretransplantation samples, patients showed a significantly higher sCD30 than healthy controls. The pretransplantation and posttransplantation (day-15) sCD30 levels were significantly elevated in rejecting patients compared to non-rejecting patients. No significant differences among immunosuppressive regimens were found in posttransplantation sCD30 levels. High pretransplantation and posttransplantation (day 15) sCD30 levels are associated with increased risk of early AR, and sCD30 can be another tool to evaluate immunological risk prior to kidney transplantation. There was no difference in immunosuppressive regimens used in this study on posttransplantation sCD30 levels at the first month.
在本研究中,我们调查了移植前后sCD30监测对早期(<6个月)急性排斥反应(AR)风险的影响,并分析了不同免疫抑制方案对肾移植受者移植后sCD30水平的作用。本回顾性队列研究纳入了50例接受同种异体肾移植的患者和10例健康供者。8例患者发生了经活检证实的AR(19%)。在移植前样本中,患者的sCD30水平显著高于健康对照。与未发生排斥反应的患者相比,发生排斥反应的患者移植前和移植后(第15天)的sCD30水平显著升高。免疫抑制方案之间在移植后sCD30水平上未发现显著差异。移植前和移植后(第15天)的高sCD30水平与早期AR风险增加相关,并且sCD30可作为肾移植前评估免疫风险的另一种工具。本研究中使用的免疫抑制方案在第1个月时对移植后sCD30水平没有差异。