Stallone Giovanni, Infante Barbara, Schena Antonio, Battaglia Michele, Ditonno Pasquale, Loverre Antonia, Gesualdo Loreto, Schena Francesco Paolo, Grandaliano Giuseppe
Department of Biomedical Sciences, Division of Nephrology, University of Foggia, Foggia, Italy.
J Am Soc Nephrol. 2005 Dec;16(12):3755-62. doi: 10.1681/ASN.2005060635. Epub 2005 Oct 19.
Chronic allograft nephropathy (CAN) represents the main cause of renal allograft loss after 1 yr of transplantation. Calcineurin inhibitor (CNI) use is associated with increased graft expression of profibrotic cytokines, whereas rapamycin inhibits fibroblast proliferation. The aim of this randomized, prospective, open-label, single-center study was to evaluate the histologic and clinical effect of rapamycin on biopsy-proven CAN. Eighty-four consecutive patients who had biopsy-proven CAN and received a transplant were randomized to receive either a 40% CNI reduction plus mycophenolate mofetil (group 1; 50 patients) or immediate CNI withdrawal and rapamycin introduction with a loading dose of 0.1 mg/kg per d and a maintaining dose aiming at through levels of 6 to 10 ng/ml (group 2; 34 patients). The follow-up period was 24 mo. At the end of follow-up, 25 patients (group 1, 10 patients; group 2, 15 patients) underwent a second biopsy. CAN lesions were graded according to Banff criteria. alpha-Smooth muscle actin (alpha-SMA) protein expression was evaluated in all biopsies as a marker of fibroblast activation. Graft function and Banff grading were superimposable at randomization. Graft survival was significantly better in group 2 (P = 0.0376, chi2 = 4.323). CAN grading worsened significantly in group 1, whereas it remained stable in group 2. After 24 mo, all group 1 biopsies showed an increase of alpha-SMA expression at the interstitial and vascular levels (P < 0.001); on the contrary, alpha-SMA expression was dramatically reduced in group 2 biopsies (P = 0.005). This study demonstrates that rapamycin introduction/CNI withdrawal improves graft survival and reduces interstitial and vascular alpha-SMA expression, slowing down the progression of allograft injury in patients with CAN.
慢性移植肾肾病(CAN)是移植1年后移植肾丢失的主要原因。使用钙调神经磷酸酶抑制剂(CNI)会使移植肾中促纤维化细胞因子的表达增加,而雷帕霉素可抑制成纤维细胞增殖。这项随机、前瞻性、开放标签、单中心研究的目的是评估雷帕霉素对经活检证实的CAN的组织学和临床效果。84例经活检证实患有CAN且接受移植的连续患者被随机分为两组,一组为CNI剂量减少40%加霉酚酸酯(第1组,50例患者),另一组为立即停用CNI并引入雷帕霉素,负荷剂量为每天0.1mg/kg,维持剂量目标是使血药浓度达到6至10ng/ml(第2组,34例患者)。随访期为24个月。随访结束时,25例患者(第1组10例,第2组15例)接受了第二次活检。根据班夫标准对CAN病变进行分级。在所有活检中评估α平滑肌肌动蛋白(α-SMA)蛋白表达,作为成纤维细胞活化的标志物。随机分组时移植肾功能和班夫分级具有可比性。第2组的移植肾存活率显著更高(P = 0.0376,χ2 = 4.323)。第1组的CAN分级显著恶化,而第2组保持稳定。24个月后,第1组所有活检均显示间质和血管水平的α-SMA表达增加(P < 0.001);相反,第2组活检中α-SMA表达显著降低(P = 0.005)。本研究表明,引入雷帕霉素/停用CNI可提高移植肾存活率,降低间质和血管α-SMA表达,减缓CAN患者移植肾损伤的进展。