Bierke P
Acta Radiol Oncol. 1986 Mar-Apr;25(2):147-54. doi: 10.3109/02841868609136394.
The role of long-time immune suppression in carcinogenesis induced by the long-lived internal emitter 90Sr, is investigated in an ongoing study. The experimental design is based on the assumption that impaired immune responsiveness, by other means than 90Sr, might increase the neoplastic response in exposed individuals, and thus reflect a protective function, if existing. Intercomparison is made of the tumour yield in mice exposed to different single doses of 90Sr and simultaneously subjected or not to long-term immune suppression by adult thymectomy (ATx) and/or antilymphocyteglobulin (ALG) treatment. Information on the general condition and responsiveness of the immune system, in the respective models, during tumour expectancy time, is essential for a conclusive evaluation of the results. To meet these demands the present paper reports on histopathologic alterations in immune organs and changes in white blood cell counts, induced by the different combinations of 90Sr, ATx and ALG treatment. The results confirm the prediction, that ATx + ALG is an efficient and, with respect to the purpose of the study, suitable treatment for additive long-term depression of the immune system in 90Sr irradiated mice, evidenced in particular by increased depletion of monomorphonuclear cells (MNC) in lymphoid organs and peripheral blood. Subsequent reports will deal with functional immune parameters.
在一项正在进行的研究中,对长期免疫抑制在由长寿命内照射源90Sr诱发癌症过程中的作用进行了调查。实验设计基于这样一种假设:通过90Sr以外的其他方式导致的免疫反应受损,可能会增加受照射个体的肿瘤反应,因此,如果存在这种保护功能,就能反映出来。对接受不同单剂量90Sr照射且同时接受或未接受成年胸腺切除(ATx)和/或抗淋巴细胞球蛋白(ALG)治疗以进行长期免疫抑制的小鼠的肿瘤发生率进行了比较。在肿瘤预期发生期间,了解各个模型中免疫系统的总体状况和反应性,对于最终评估结果至关重要。为满足这些要求,本文报告了由90Sr、ATx和ALG治疗的不同组合所诱导的免疫器官组织病理学改变以及白细胞计数的变化。结果证实了以下预测:对于本研究目的而言,ATx + ALG是一种有效且合适的治疗方法,可用于对90Sr照射小鼠的免疫系统进行长期累加性抑制,尤其表现为淋巴器官和外周血中单核细胞(MNC)的耗竭增加。后续报告将探讨功能性免疫参数。