应用激光流式细胞术和单克隆抗体(免疫细胞术)分析肾移植患者的临床白细胞表型。

Diagnostic immunology Pub Date : 1986-01-01
R Mazaheri, C R Stiller, P A Keown
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引用次数: 0

摘要

采用免疫细胞术对54例连续接受硫唑嘌呤/强的松(STD gp, N = 16)或环孢素加或不加强的松(CsA gp, N = 38)的同种异体肾移植前后的外周血单核细胞绝对水平进行了监测。在接受性病治疗的CsA组中,除了OKT4+细胞外,所有细胞的平均绝对水平都随着治疗时间的延长而显著增加。在两个治疗组(STD + CsA)中,平均% δ OKT4/8比值从射血前静止值80 +/- 6% SE增加到排斥值120 +/- 6% (P小于0.001),并在射血后静止中回落到77 +/- 6% (P小于0.0005)。该比值升高对排斥反应的敏感性为84.4%,特异性为88.6%,阳性似然比为7.40,阴性似然比为0.15。在排斥反应中,伴随的免疫病理学显示移植物中OKT8+细胞占优势,肾活检的平均T细胞亚群比为0.8 +/- 0.3 SE,而循环细胞的平均T细胞亚群比为2.0 +/- 0.3 SE (P小于0.0125)。淋巴细胞介导的细胞毒性(LMC)平行供体抗原特异性测定在移植排斥反应中呈阳性。因此,纵向分析中序列数据归一化的免疫细胞术似乎是免疫实验室监测移植排斥反应的一种有价值的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical leukocyte phenotyping by laser flow cytometry and monoclonal antibodies (immunocytometry) in renal transplantation.

Absolute levels of peripheral blood mononuclear cells were sequentially monitored by immunocytometry in 54 consecutive renal allograft recipients receiving azathioprine/prednisone (STD gp, N = 16) or cyclosporine with or without prednisone (CsA gp, N = 38), before and after transplantation. In the CsA group, but not in those receiving STD therapy, the mean absolute levels of all but OKT4+ cells increased significantly with the duration of therapy. In both treatment groups (STD + CsA), the mean % delta OKT4/8 ratio increased from a prerejection quiescent value of 80 +/- 6% SE to a rejection value of 120 +/- 6% (P less than .001) and fell back to 77 +/- 6% (P less than .0005) in postrejection quiescence. The sensitivity and specificity of such an elevated ratio for rejection were 84.4% and 88.6%, while positive and negative likelihood ratios were 7.40 and 0.15, respectively. In rejection, concomitant immunopathology showed a predominance of OKT8+ cells in the graft with a mean T cell subset ratio of 0.8 +/- 0.3 SE in renal biopsies compared to 2.0 +/- 0.3 for circulating cells (P less than .0125). Parallel donor-antigen-specific assay of lymphocyte-mediated cytotoxicity (LMC) became positive with graft rejection. Immunocytometry with normalization of sequential data in longitudinal analysis thus appears to be a valuable tool in immunologic laboratory monitoring of graft rejection.

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