Zembala M, Ptak W, Hanczakowska M
Immunology. 1973 Oct;25(4):631-44.
Lymph node and spleen cells from normal mice were cultured for 3 days with polyoma virus-induced tumour, Ehrlich's ascites tumour or leukaemia L 1210 cells. This resulted in immunization of the lymphocytes, which were then transferred to irradiated target cells labelled with Cr. Normal, i.e. non-immune thioglycollate-stimulated peritoneal macrophages were also added to some tubes. Non-immune macrophages mixed with immunized lymphocytes showed a significantly increased ability to destroy tumour cells as compared with macrophages in the absence of immunized lymphocytes. The immunized lymphocytes were almost entirely inactive alone. When the number of macrophages was kept constant the cytotoxicity was dependent on the number of viable immunized lymphocytes placed on the target cells. Immunized lymphocytes, in the presence of macrophages, only exhibited strong killing of the target cells against which they had been immunized; some lysis of bystander' cells was, however, seen provided specific target cells were present. Macrophage monolayers exposed to immunized lymphocytes upon contact with specific antigen became armed' and showed a significant cytotoxicity for specific target cells. When immunized lymphocytes and normal macrophages were treated with actinomycin D and puromycin, cytotoxicity was inhibited in the immunized lymphocytes but not in the macrophages. The possible mechanism of normal macrophage cooperation with immunized lymphocytes in the cytotoxic killing reaction is discussed. Results presented in this paper favour the view that immunologically specific cytophilic factor (presumptive cytophilic antibody) is involved in the macrophage-mediated cytotoxicity in the system studied.
将正常小鼠的淋巴结和脾细胞与多瘤病毒诱导的肿瘤细胞、艾氏腹水瘤细胞或白血病L1210细胞一起培养3天。这导致淋巴细胞被免疫,然后将其转移到用铬标记的经辐照的靶细胞中。在一些试管中还加入了正常的、即未免疫的巯基乙酸盐刺激的腹腔巨噬细胞。与不存在免疫淋巴细胞时的巨噬细胞相比,与免疫淋巴细胞混合的未免疫巨噬细胞破坏肿瘤细胞的能力显著增强。单独的免疫淋巴细胞几乎完全没有活性。当巨噬细胞数量保持恒定时,细胞毒性取决于放置在靶细胞上的存活免疫淋巴细胞的数量。在巨噬细胞存在的情况下,免疫淋巴细胞仅对其已被免疫的靶细胞表现出强烈的杀伤作用;然而,如果存在特异性靶细胞,也会观察到一些“旁观者”细胞的裂解。与特异性抗原接触后暴露于免疫淋巴细胞的巨噬细胞单层会“武装”起来,并对特异性靶细胞表现出显著的细胞毒性。当用放线菌素D和嘌呤霉素处理免疫淋巴细胞和正常巨噬细胞时,免疫淋巴细胞的细胞毒性受到抑制,但巨噬细胞不受影响。本文讨论了正常巨噬细胞与免疫淋巴细胞在细胞毒性杀伤反应中协同作用的可能机制。本文给出的结果支持这样一种观点,即免疫特异性亲细胞因子(推测为亲细胞抗体)参与了所研究系统中巨噬细胞介导的细胞毒性作用。