Mangge H, Beaufort F, Kaulfersch W, Rossipal E, Schauenstein K
Department of Pediatrics, School of Medicine, University of Graz, Austria.
J Cancer Res Clin Oncol. 1990;116(6):575-80. doi: 10.1007/BF01637077.
The purpose of this study was to examine patterns of peripheral T-cell-activation antigen expression after polyclonal in vitro stimulation in early stages of lymphoproliferative diseases. With 18 patients afflicted with recently diagnosed, non-leukemic stages of B and T cell lymphoma cytofluorimetric analysis was performed with peripheral blood lymphocytes (PBL) after 72 h in culture with and without phytohemagglutinin, using antibodies against the differentiation antigens CD3, CD8, CD4, CD16, CD19, CDw14, and the activation antigens interleukin-2 receptor (IL-2R, CD25), HLA-DR (DR), CD56 and transferrin receptor (TR). Compared to healthy controls and patients with other diseases, a very significant reduction of large T cells bearing activation markers was found in all lymphoma cases. Furthermore, a pronounced inhibition in the expression of the activation markers IL-2R and TR, but not of DR, was detected on CD3+ cells in phytohemagglutinin-stimulated PBL of all lymphoma cells independently of DNA synthesis, as measured by [3H]thymidine uptake. Determination of the natural-killer-cell-(NK)-associated antigens CD16 and CD56, available for our studies in a CD16 + CD56 combination kit, revealed, after phytohemagglutinin stimulation, significantly increased expression values in 8 lymphoma patients so far investigated, as compared to 12 healthy controls. Thus, polyclonal activation combined with cytofluorimetric screening of activation antigens seems to give useful information on the functional defect(s) of PBL in an early state of lymphoma, and may therefore be of considerable diagnostic value. The observed pattern of T cell activation antigen expression after phytohemagglutinin stimulation may give further clues to the understanding of immune dysfunction(s) associated with lymphoma.
本研究的目的是检测淋巴细胞增殖性疾病早期多克隆体外刺激后外周血T细胞活化抗原的表达模式。对18例近期诊断为非白血病期的B细胞和T细胞淋巴瘤患者,将外周血淋巴细胞(PBL)在有或没有植物血凝素的情况下培养72小时后,使用针对分化抗原CD3、CD8、CD4、CD16、CD19、CDw14以及活化抗原白细胞介素-2受体(IL-2R,CD25)、HLA-DR(DR)、CD56和转铁蛋白受体(TR)的抗体进行细胞荧光分析。与健康对照和其他疾病患者相比,在所有淋巴瘤病例中均发现带有活化标记的大T细胞显著减少。此外,在所有淋巴瘤细胞经植物血凝素刺激的PBL中,通过[3H]胸腺嘧啶核苷摄取测定,发现CD3+细胞上活化标记IL-2R和TR的表达受到明显抑制,但DR不受影响,且与DNA合成无关。通过可用于我们研究的CD16 + CD56组合试剂盒测定自然杀伤细胞(NK)相关抗原CD16和CD56,结果显示,与12名健康对照相比,在目前研究的8例淋巴瘤患者中,植物血凝素刺激后其表达值显著增加。因此,多克隆激活结合活化抗原的细胞荧光筛选似乎能为淋巴瘤早期PBL功能缺陷提供有用信息,因而可能具有相当大的诊断价值。植物血凝素刺激后观察到的T细胞活化抗原表达模式可能为理解与淋巴瘤相关的免疫功能障碍提供进一步线索。