Spriewald B M, Hara M, Bushell A, Jenkins S, Morris P J, Wood K J
Nuffield Department of Surgery, University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom.
Am J Pathol. 2000 Nov;157(5):1453-8. doi: 10.1016/S0002-9440(10)64783-9.
The early and reliable diagnosis of allograft rejection is a difficult task and the assessment of cytokine expression in the grafts can be a helpful parameter. We have compared competitive reverse transcriptase-polymerase chain reaction (RT-PCR) with intracellular cytokine staining by flow cytometry as tools to measure cytokine expression in rejecting and nonrejecting murine cardiac allografts. Both techniques gave comparable results for cytokine expression in rejecting allografts and syngeneic controls. Grafts from mice pretreated with anti-CD4 antibody and donor-specific blood transfusion showed a marked reduction in cytokine expression, as assessed by competitive RT-PCR, even though a cellular infiltrate was present in the graft. In contrast, the cytokine production measured by intracellular cytokine staining of the isolated graft-infiltrating cells was high and exceeded even that of the rejecting allografts. We conclude that intracellular cytokine staining of graft-infiltrating leukocytes by flow cytometry does not necessarily reflect accurately the cytokine milieu in the graft. This technique might therefore have a limited clinical application in contrast to competitive RT-PCR for the differentiation between graft acceptance and graft rejection.
同种异体移植排斥反应的早期可靠诊断是一项艰巨任务,评估移植物中的细胞因子表达可能是一个有用的参数。我们比较了竞争性逆转录聚合酶链反应(RT-PCR)与流式细胞术检测细胞内细胞因子染色,以此作为测量排斥和未排斥小鼠心脏同种异体移植物中细胞因子表达的工具。两种技术在排斥性同种异体移植物和同基因对照中的细胞因子表达方面给出了可比的结果。通过竞争性RT-PCR评估,用抗CD4抗体和供体特异性输血预处理的小鼠的移植物,尽管移植物中存在细胞浸润,但细胞因子表达显著降低。相比之下,通过对分离的移植物浸润细胞进行细胞内细胞因子染色测量的细胞因子产生量很高,甚至超过了排斥性同种异体移植物。我们得出结论,流式细胞术检测移植物浸润白细胞的细胞内细胞因子染色不一定能准确反映移植物中的细胞因子环境。因此,与竞争性RT-PCR相比,该技术在区分移植物接受和移植物排斥方面的临床应用可能有限。