Cinti Paola, Pretagostini Renzo, Arpino Alessia, Tamburro Maria Luisa, Mengasini Sonia, Lattanzi Roberto, De Simone Paolo, Berloco Pasquale, Molajoni Elvira Renna
General and Transplant Surgery, La Sapienza University of Rome, Policlinico Umberto I, Rome, Italy.
Transplantation. 2005 May 15;79(9):1154-6.
To retrospectively compare the accuracy of pretransplant panel of reactivity antibodies (PRA) and serum level of soluble CD30 (sCD30) in predicting early (<6 months) acute rejection (AR) in living-donor and deceased-donor kidney-transplant (KT) patients.
Pretransplant sera of 24 KT recipients were retrospectively tested for sCD30 and compared with PRA. Inclusion criteria were de novo graft patients on calcineurin-inhibitor-based immunosuppression, minimum follow-up of 1 year, alive with a functioning graft, and stable renal function over the last 12 months. Objective measures were incidence of biopsy-proven AR (BPAR) within 6 months of KT and sCD30 and PRA diagnostic indexes. The relative risk (RR) of BPAR for each test was also obtained.
Fourteen (58.3%) patients presented at least one episode of BPAR within 6 months of KT. All rejection episodes were responsive to steroid treatment. PRA was positive in six (25%) patients, and four (66.7%) of them presented at least one episode of BPAR. sCD30 tested positive in nine (37.5%) patients, and all these later presented at least one episode of BPAR. sCD30 and PRA diagnostic indexes in predicting early (< 6months) BPAR were sensitivity 64.2% versus 28.5%; specificity 100% versus 80%; accuracy 79.1% versus 50%; positive predictive value 100% versus 66.6%; and negative predictive value 66.6% versus 44.4%. The RR of early AR was 1.4 in PRA-positive patients and extremely higher in the sCD30-positive group.
Pretransplant sCD30 is a more accurate predictor of AR when compared with PRA. These results support its use in the pretransplant work-up of kidney-graft recipients.
回顾性比较移植前反应性抗体检测(PRA)和可溶性CD30(sCD30)血清水平在预测活体供肾和尸体供肾肾移植(KT)受者早期(<6个月)急性排斥反应(AR)中的准确性。
回顾性检测24例KT受者移植前血清中的sCD30,并与PRA进行比较。纳入标准为接受基于钙调神经磷酸酶抑制剂的免疫抑制治疗的初发移植患者,至少随访1年,移植肾存活且功能良好,以及在过去12个月内肾功能稳定。客观指标为KT后6个月内活检证实的AR(BPAR)发生率以及sCD30和PRA诊断指标。还获得了每项检测的BPAR相对风险(RR)。
14例(58.3%)患者在KT后6个月内出现至少1次BPAR发作。所有排斥反应均对类固醇治疗有反应。6例(25%)患者PRA呈阳性,其中4例(66.7%)出现至少1次BPAR发作。9例(37.5%)患者sCD30检测呈阳性,所有这些患者随后均出现至少1次BPAR发作。sCD30和PRA在预测早期(<6个月)BPAR方面的诊断指标分别为:敏感性64.2%对28.5%;特异性100%对80%;准确性79.1%对50%;阳性预测值100%对66.6%;阴性预测值66.6%对44.4%。PRA阳性患者早期AR的RR为1.4,而sCD30阳性组则极高。
与PRA相比,移植前sCD30是AR更准确的预测指标。这些结果支持将其用于肾移植受者的移植前检查。