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肿瘤免疫疗法的实验研究。I. 巨噬细胞移动抑制活性作为一项免疫学参数。

Experimental studies of tumor immunotherapy. I. Macrophage migration inhibitory activity as an immunological parameter.

作者信息

Hayashi S

出版信息

Acta Med Okayama. 1976 Apr;30(2):95-106.

PMID:135489
Abstract

The macrophage migration inhibition activity [MI activity) was stable in sensitized lymphocyte-to-marcophage ratios of 1:5 to 1:20 in mice. Antigen protein concentrations under 100 mug/ml did not induce nonspecific macrophage migration inhibition. Inhibition of tumor proliferation and survival was observed after a combined injection of BCG and MH-134 cells. After a single injection of MH-134 tumor cells, MI activity was reinforced and prolonged, demonstrating the clear effects of BCG as adjuvant. In DDS mice MI activity was weakened in the regional lymph node after a subcutaneous injection of just above or below 10(5) Ehrlich cancer cells previously treated with mitomycin C. This finding suggests the presence of an optimal tumor antigen concentration.

摘要

在小鼠中,巨噬细胞移动抑制活性(MI活性)在致敏淋巴细胞与巨噬细胞比例为1:5至1:20时保持稳定。100μg/ml以下的抗原蛋白浓度不会诱导非特异性巨噬细胞移动抑制。在联合注射卡介苗(BCG)和MH-134细胞后,观察到肿瘤增殖和存活受到抑制。单次注射MH-134肿瘤细胞后,MI活性增强且持续时间延长,表明BCG作为佐剂具有明显效果。在DDS小鼠中,皮下注射经丝裂霉素C预处理的略高于或低于10⁵个艾氏癌细胞后,区域淋巴结中的MI活性减弱。这一发现提示存在最佳肿瘤抗原浓度。

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