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在6个月方案活检中未经治疗的排斥反应与系列活检中的纤维化或移植物功能丧失无关。

Untreated rejection in 6-month protocol biopsies is not associated with fibrosis in serial biopsies or with loss of graft function.

作者信息

Scholten Eduard M, Rowshani Ajda T, Cremers Serge, Bemelman Frederike J, Eikmans Michael, van Kan Erik, Mallat Marko J, Florquin Sandrine, Surachno Janto, ten Berge Ineke J, Bajema Ingeborg M, de Fijter Johan W

机构信息

Department of Nephrology, Leiden University Medical Center, PO Box 9600, 2300 RC Leiden, The Netherlands.

出版信息

J Am Soc Nephrol. 2006 Sep;17(9):2622-32. doi: 10.1681/ASN.2006030227. Epub 2006 Aug 9.

Abstract

Donor age, calcineurin inhibitor nephrotoxicity, and acute rejection are the most significant predictors of chronic allograft nephropathy. Protocol biopsies, both in deceased- and living-donor renal grafts, have shown that cortical tubulointerstitial fibrosis correlates with graft survival and function. The impact of not treating subclinical acute rejection (SAR) is less clear. In this study, 126 de novo renal transplant recipients were randomly assigned to receive area-under-the-curve-controlled exposure of either a cyclosporine or a tacrolimus-based immunosuppressive regimen that included steroids, mycophenolate mofetil, and basiliximab induction. Protocol biopsies were taken before and 6 and 12 mo after transplantation. The prevalence of SAR was determined retrospectively. Fibrosis was evaluated by quantitative digital analysis of Sirius red staining in serial biopsies. Donor age correlated significantly with tubulointerstitial fibrosis in pretransplantation biopsies and inferior graft function at month 6 (rtau = -0.26; P = 0.033). Acute rejection incidence was 11.5%, and no clinical late rejection occurred. The prevalence of SAR at 6 mo was 30.8% but was not associated with differences in serial quantitative Sirius red staining at 6 or 12 mo, proteinuria, or progressive loss of GFR up to 2 yr. No differences were found in donor variables, histocompatibility, rejection history, or exposure of immunosuppressants. Controlled individualized calcineurin inhibitor exposure and subsequent tapering resulted in a low early acute rejection rate and prevented late acute rejection. Because, by design, we did not treat SAR, these results provide evidence that asymptomatic infiltrates in 6-mo surveillance biopsies may not be deleterious in the intermediate term. There is need for reliable biomarkers to prove that not all cell infiltrates are equivalent or that infiltrates may change with time.

摘要

供体年龄、钙调神经磷酸酶抑制剂肾毒性和急性排斥反应是慢性移植肾肾病最重要的预测因素。对尸体供肾和活体供肾移植进行的方案活检均显示,皮质肾小管间质纤维化与移植肾的存活及功能相关。对于未治疗亚临床急性排斥反应(SAR)的影响,目前尚不清楚。在本研究中,126例初次接受肾移植的受者被随机分配,接受基于环孢素或他克莫司的免疫抑制方案,该方案包括类固醇、霉酚酸酯和巴利昔单抗诱导治疗,其药物暴露量通过曲线下面积进行控制。在移植前、移植后6个月和12个月进行方案活检。回顾性确定SAR的发生率。通过对连续活检中天狼星红染色进行定量数字分析来评估纤维化情况。供体年龄与移植前活检中的肾小管间质纤维化以及术后6个月时移植肾功能较差显著相关(rtau = -0.26;P = 0.033)。急性排斥反应发生率为11.5%,未发生临床晚期排斥反应。6个月时SAR的发生率为30.8%,但与6个月或12个月时连续定量天狼星红染色、蛋白尿或长达2年的肾小球滤过率逐渐下降的差异无关。在供体变量、组织相容性、排斥反应史或免疫抑制剂暴露方面未发现差异。控制个体化的钙调神经磷酸酶抑制剂暴露并随后逐渐减量,导致早期急性排斥反应率较低,并预防了晚期急性排斥反应。由于按照设计我们未治疗SAR,这些结果表明,6个月监测活检中无症状浸润在中期可能并无危害。需要可靠的生物标志物来证明并非所有细胞浸润都是等同的,或者浸润可能随时间变化。

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