Griffiths G M, Namikawa R, Mueller C, Liu C C, Young J D, Billingham M, Weissman I
Department of Pathology, Stanford University School of Medicine.
Eur J Immunol. 1991 Mar;21(3):687-93. doi: 10.1002/eji.1830210322.
The use of granzyme A and perforin as markers for rejection after cardiac transplantation has been investigated. Using in situ hybridization we have detected lymphocytes expressing granzyme A and perforin RNA that are infiltrating the donor heart after transplantation. A total of 29 different biopsies from 17 different patients who had undergone cardiac transplantation were examined. Twelve biopsies classified by conventional histological criteria as showing evidence of rejection were found to contain lymphocytes expressing granzyme A and perforin. Seven biopsies classified as showing no histological evidence of rejection infiltrating lymphocytes were found not to be expressing granzyme A or perforin. However, in 10 other biopsies from 5 different patients that had been classified as showing no evidence of rejection by the conventional grading system, lymphocytes expressing granzyme A and perforin were detected. In six of these cases the patient was found to have undergone a subsequent rejection episode. In the other four cases the biopsies were either taken at a very early stage after transplantation and the high doses of immunosuppression used routinely at that stage are likely to have averted any rejection episodes, or it was not possible to follow subsequent rejection episodes. These results, which are statistically significant (p = 0.06), demonstrate that granzyme A- and perforin-expressing lymphocytes can be identified in rejecting biopsies before histological damage is seen. The identification of perforin and granzyme A expression in vivo suggest a possible role for these proteins in the cytolysis that occurs during transplantation rejection. Furthermore, the data presented here suggest that it may be possible to use granzyme A and perforin as early predictive markers of transplantation rejection.
已对将颗粒酶A和穿孔素用作心脏移植后排斥反应标志物进行了研究。通过原位杂交,我们检测到移植后浸润供体心脏的表达颗粒酶A和穿孔素RNA的淋巴细胞。共检查了17例接受心脏移植的不同患者的29份不同活检样本。12份根据传统组织学标准分类为有排斥反应证据的活检样本中发现含有表达颗粒酶A和穿孔素的淋巴细胞。7份分类为无组织学排斥反应证据的活检样本中未发现浸润淋巴细胞表达颗粒酶A或穿孔素。然而,在5例不同患者的另外10份活检样本中,根据传统分级系统分类为无排斥反应证据,但检测到了表达颗粒酶A和穿孔素的淋巴细胞。其中6例患者随后发生了排斥反应。在另外4例中,活检样本要么是在移植后非常早期采集的,当时常规使用的高剂量免疫抑制可能避免了任何排斥反应,要么无法追踪随后的排斥反应。这些结果具有统计学意义(p = 0.06),表明在出现组织学损伤之前,可在有排斥反应的活检样本中识别出表达颗粒酶A和穿孔素的淋巴细胞。体内穿孔素和颗粒酶A表达的鉴定表明这些蛋白质在移植排斥反应期间发生 的细胞溶解中可能发挥作用。此外,此处给出的数据表明,可能可以将颗粒酶A和穿孔素用作移植排斥反应的早期预测标志物。