Dörge S E, Roux-Lombard P, Dayer J M, Koch K M, Frei U, Lonnemann G
Department of Nephrology, Medizinische Hochschule Hannover, Germany.
Transplantation. 1994 Nov 15;58(9):1000-8. doi: 10.1097/00007890-199411150-00005.
Tumor necrosis factor-alpha is elevated in plasma during kidney transplant rejection. However, the measurement and biological activity of TNF alpha is influenced by inhibitory soluble TNF receptors. We therefore determined plasma levels of TNF alpha and the 2 soluble TNF receptors, the 55-kDa TNF receptor (TNF-sR55) and the 75-kDa TNF receptor (TNF-sR75), by immunoassays in 25 patients before and daily after kidney transplantation. Plasma samples were retrospectively assigned to 3 groups: (1) patients with well-functioning grafts (n = 14); (2) patients with biopsy-proven graft rejections (n = 7 patients with 10 rejections); and (3) patients with episodes of CsA nephrotoxicity (n = 4 patients with 9 samples). On the day of biopsy-proven graft rejection, TNF alpha increased from 8.6 +/- 0.9 pg/ml to 14.8 +/- 3.5 pg/ml (P < 0.02), TNF-sR55 from 6.6 +/- 1.3 ng/ml to 9.0 +/- 1.2 ng/ml (NS), and TNF-sR75 from 10.3 +/- 1.0 ng/ml to 15.3 +/- 2.0 ng/ml (P < 0.01). During episodes of CsA toxicity, TNF alpha levels did not change, TNF-sR55 increased from 5.2 +/- 0.5 ng/ml to 10.5 +/- 0.5 ng/ml (P < 0.01), and TNF-sR75 increased from 10.2 +/- 0.8 ng/ml to 17.5 +/- 0.9 ng/ml (P < 0.01). There was a strong correlation between serum creatinine and plasma TNF-sR55 (r = 0.7, P < 0.001) and TNF-sR75 (r = 0.7, P < 0.001), but not with TNF alpha. Therefore, levels of TNF-sR55 and TNF-sR75 were corrected for serum creatinine. An index expressing TNF alpha over actively released soluble receptors (index = TNF alpha/(corr.TNF-sR55 + corr.TNF-sR75)) detected rejection episodes with a sensitivity of 70-80% and a specificity of 89%. We conclude that the measurement of plasma TNF alpha in combination with its soluble receptors is superior to isolated TNF alpha determinations in discriminating acute graft rejection from episodes of CsA toxicity in kidney transplant recipients.
在肾移植排斥反应期间,血浆中肿瘤坏死因子-α(TNF-α)水平会升高。然而,TNF-α的测量及生物活性会受到可溶性TNF受体抑制剂的影响。因此,我们通过免疫测定法测定了25例患者肾移植术前及术后每日血浆中TNF-α以及两种可溶性TNF受体,即55 kDa TNF受体(TNF-sR55)和75 kDa TNF受体(TNF-sR75)的水平。血浆样本被回顾性分为3组:(1)移植肾功能良好的患者(n = 14);(2)经活检证实有移植排斥反应的患者(n = 7,共10次排斥反应);(3)发生环孢素A(CsA)肾毒性的患者(n = 4,共9份样本)。在经活检证实有移植排斥反应当天,TNF-α从8.6±0.9 pg/ml升至14.8±3.5 pg/ml(P < 0.02),TNF-sR55从6.6±1.3 ng/ml升至9.0±1.2 ng/ml(无统计学意义),TNF-sR75从10.3±1.0 ng/ml升至15.3±2.0 ng/ml(P < 0.01)。在CsA毒性发作期间,TNF-α水平未变化,TNF-sR55从5.2±0.5 ng/ml升至10.5±0.5 ng/ml(P < 0.01),TNF-sR75从10.2±0.8 ng/ml升至17.5±0.9 ng/ml(P < 0.01)。血清肌酐与血浆TNF-sR55(r = 0.7,P < 0.001)和TNF-sR75(r = 0.7,P < 0.001)之间存在强相关性,但与TNF-α无相关性。因此,对TNF-sR55和TNF-sR75的水平进行了血清肌酐校正。一个表示TNF-α相对于活性释放的可溶性受体的指数(指数 = TNF-α/(校正后的TNF-sR55 + 校正后的TNF-sR75))检测排斥反应发作的敏感性为70 - 80%,特异性为89%。我们得出结论,在区分肾移植受者的急性移植排斥反应和CsA毒性发作方面,联合测量血浆TNF-α及其可溶性受体优于单独测定TNF-α。