Cunningham A C, Kirby J A, Colquhoun I W, Flecknell P A, Ashcroft T, Dark J H
Department of Surgery, Medical School, University of Newcastle upon Tyne.
Thorax. 1994 Feb;49(2):151-6. doi: 10.1136/thx.49.2.151.
At present the diagnosis of pulmonary allograft rejection is made after examination of transbronchial biopsy specimens; this method is highly invasive. A study was performed to determine whether immunological parameters measured in peripheral blood or bronchoalveolar lavage samples correlate with the histological diagnosis of rejection.
Left unilateral pulmonary allotransplantation was performed between dogs. The animals were immunosuppressed with cyclosporin A after transplantation but the dose of this drug was gradually reduced to allow controlled rejection to take place. Rejection was diagnosed histologically. Four immunological parameters were investigated: measurement of lavage derived T cell proliferation in response to limited culture with interleukin 2; measurement of changes in the frequency of donor reactive cytotoxic T lymphocytes; assay of the level of donor cell binding IgG antibody in recipient plasma; and measurement of the antibody dependent cell mediated cytotoxic response to donor cells after labelling with recipient plasma.
Assays based on measurement of the function of T cells produced significant results at a time later than the histological diagnosis of severe rejection. The level of donor reactive IgG antibody increased at a time that corresponded closely with the diagnosis of severe rejection. This IgG did not activate the antibody dependent cell mediated cytotoxic effector mechanism to a significant extent.
Measurement of parameters of donor specific immunoreactivity can yield data which are indicative of severe pulmonary allograft rejection. These methods make use of samples which can be obtained by minimally invasive methods. Measurement of the plasma level of donor reactive IgG antibody appears to be the most useful assay. However, each of the in vitro assays used during this series of experiments was less sensitive to the onset of rejection than was routine histological examination.
目前,肺移植排斥反应的诊断是在经支气管活检标本检查后做出的;这种方法具有高度侵入性。进行了一项研究,以确定在外周血或支气管肺泡灌洗样本中测量的免疫参数是否与排斥反应的组织学诊断相关。
在犬之间进行左单侧肺同种异体移植。动物在移植后用环孢素A进行免疫抑制,但逐渐降低该药物的剂量以允许可控的排斥反应发生。通过组织学诊断排斥反应。研究了四个免疫参数:测量灌洗来源的T细胞在白细胞介素2有限培养下的增殖;测量供体反应性细胞毒性T淋巴细胞频率的变化;测定受体血浆中供体细胞结合IgG抗体的水平;以及测量用受体血浆标记后对供体细胞的抗体依赖性细胞介导的细胞毒性反应。
基于T细胞功能测量的检测在严重排斥反应的组织学诊断之后的时间产生了显著结果。供体反应性IgG抗体水平在与严重排斥反应诊断密切对应的时间升高。这种IgG在很大程度上没有激活抗体依赖性细胞介导的细胞毒性效应机制。
测量供体特异性免疫反应性参数可以产生指示严重肺移植排斥反应的数据。这些方法利用的样本可以通过微创方法获得。测量供体反应性IgG抗体的血浆水平似乎是最有用的检测方法。然而,在这一系列实验中使用的每种体外检测方法对排斥反应发生的敏感性都低于常规组织学检查。