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Tumour Growth and Non-Specific Immunity in Rats: The Mechanisms Involved in Inhibition of Tumour Growth

机译:大鼠肿瘤生长和非特异性免疫:抑制肿瘤生长的机制。

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摘要

Various non-specific in vivo stimulants of phagocytosis, such as peptone, starch, glycogen, BCG, inhibit the growth of Walker carcinosarcoma in rats. This was confirmed by comparison of the histological appearance of tumour beds and tumours of peptone-treated and control rats. In rats given peptone or BCG, tumour inhibition was detectable only during a limited period of time. Experiments on the effect of pretreatment with peptone on the growth of Walker ascites tumour cells revealed a clear-cut inhibition, and suggest that tumour cells may be successfully eliminated during the lag phase. Data showing that activated macrophages labelled with 51Cr significantly accumulate around the tumour implant support the view that macrophages are of prime importance in the elimination of tumour cells in this model system.
机译:吞噬作用的各种非特异性体内刺激物,例如蛋白one,淀粉,糖原,卡介苗,均能抑制大鼠沃克癌肉瘤的生长。通过比较肿瘤床和蛋白ept治疗的和对照大鼠的肿瘤的组织学外观,证实了这一点。在接受蛋白ept或BCG的大鼠中,仅在有限的时间内可检测到肿瘤抑制作用。蛋白ept预处理对Walker腹水肿瘤细胞生长的影响的实验显示出明显的抑制作用,并表明在滞后阶段可以成功消除肿瘤细胞。数据显示,标记为 51 Cr的活化巨噬细胞大量聚集在肿瘤植入物周围,这支持了以下观点:在此模型系统中,巨噬细胞对于消除肿瘤细胞至关重要。

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