Holzinger C, Zuckermann A, Schöllhammer A, Kopp C, Imhof M, Laufer G, Griesmacher A, Zwölfer W, Laczkovics A, Wolner E
II. Chirurgische Universitätsklinik, Wien.
Wien Klin Wochenschr. 1992;104(24):748-52.
Mononuclear cells are the component of blood responsible for allograft recognition, rejection and acceptance. Shifts in the patterns of various mononuclear cell subpopulations were often used as a diagnostic tool in detection of heart rejection. The specificity of mononuclear cell monitoring has remained a controversial point until today, because infections led to similar changes as organ rejection. In this study we investigated whether mononuclear cells taken from coronary sinus blood give more information about the immunological status of the transplanted heart than those taken from central verous blood. After endomyocardial biopsy, coronary sinus blood was sampled by catheterization under X-ray control. Blood from the right atrium was taken for control measurement. Mononuclear cells obtained by density gradient cytocentrifugation were stained with monoclonal fluorescein conjugated antibodies detecting CD4- (T helper)-, CD8- (T suppressor)-, CD25- (Interleukin-2 receptor), and the CD71- (Transferrin receptor) antigens. Endomyocardial biopsies were graded according to the Billingham scheme. In the absence of rejection, the phenotypes of mononuclear cells from the coronary sinus did not differ from those of right atrial cells. Mild rejection led to a statistically insignificant increase of CD4- CD25- and CD7-antigen bearing cells in the coronary sinus blood, whereas the CD8 positive cells remained stable as compared to mononuclear cells from the right atrium. However, patients with moderate rejection showed a significant elevation of CD4 positive cells and activated T-cells (CD15-, CD71-positive cells) in the coronary sinus as compared with cells from the right atrium. The T helper/suppressor ratio (Th/s-ratio) shifted towards the T-helper population.(ABSTRACT TRUNCATED AT 250 WORDS)
单核细胞是血液中负责同种异体移植识别、排斥和接受的成分。各种单核细胞亚群模式的变化常被用作检测心脏排斥反应的诊断工具。直到今天,单核细胞监测的特异性仍然是一个有争议的问题,因为感染会导致与器官排斥反应类似的变化。在本研究中,我们调查了从冠状窦血中获取的单核细胞是否比从中央静脉血中获取的单核细胞能提供更多关于移植心脏免疫状态的信息。在心肌内膜活检后,在X射线控制下通过导管插入术采集冠状窦血。采集右心房血作为对照测量。通过密度梯度细胞离心法获得的单核细胞用检测CD4 -(辅助性T细胞)、CD8 -(抑制性T细胞)、CD25 -(白细胞介素-2受体)和CD71 -(转铁蛋白受体)抗原的单克隆荧光素偶联抗体进行染色。心肌内膜活检根据比林厄姆方案进行分级。在无排斥反应的情况下,冠状窦单核细胞的表型与右心房细胞的表型没有差异。轻度排斥反应导致冠状窦血中携带CD4 -、CD25 -和CD7抗原的细胞在统计学上无显著增加,而与右心房单核细胞相比,CD8阳性细胞保持稳定。然而,与右心房细胞相比,中度排斥反应患者的冠状窦中CD4阳性细胞和活化T细胞(CD15 -、CD71阳性细胞)显著升高。辅助性T细胞/抑制性T细胞比值(Th/s比值)向辅助性T细胞群体偏移。(摘要截短于250字)