Pels E, de Weger R A, den Otter W
Immunobiology. 1984 Jan;166(1):84-95. doi: 10.1016/S0171-2985(84)80146-1.
The phenotype of lymphocytes, obtained from mice immunized with allogeneic tumor cells, with the capacity to induce macrophage cytotoxicity was determined. Macrophage cytotoxicity was induced, either by incubating the macrophages with Macrophage Arming Factor (MAF) containing supernatants of cultures of sensitized lymphocytes and tumor cells (arming) or by incubating the macrophages directly with sensitized lymphocytes and tumor cells (activation). The MAF producing or activating capacity of the lymphocytes was not only "triggered" by the sensitizing tumor cells but also by normal cells and other tumor cells bearing the H-2 determinants of the sensitizing tumor cell. The capacity to render macrophages cytotoxic was not reduced after treatment of the lymphocytes with mitomycin-C or treatment with anti-murine Ig and complement. This capacity of the lymphocytes was abrogated after treatment with anti-T-cell serum or anti-Thy 1.2 serum and complement. After treatment with anti-Lyt 1 or anti-Lyt 2 serum and complement, the activating capacity was significantly reduced and the MAF producing capacity of the lymphocytes abrogated. Mixing the Lyt 1 depleted and Lyt 2 depleted lymphocytes or addition of normal lymphocytes to the Lyt 1 depleted or Lyt 2 depleted populations did not restore the MAF producing and activating capacities. This indicated that the lymphocytes inducing macrophage cytotoxicity in this allogeneic system are Lyt-1+2+ T-lymphocytes, which do not need to divide prior to perform their action.
对用同种异体肿瘤细胞免疫的小鼠所获得的、具有诱导巨噬细胞细胞毒性能力的淋巴细胞的表型进行了测定。巨噬细胞细胞毒性的诱导方式有两种,一种是将巨噬细胞与含有致敏淋巴细胞和肿瘤细胞培养上清液中的巨噬细胞武装因子(MAF)一起孵育(武装),另一种是将巨噬细胞直接与致敏淋巴细胞和肿瘤细胞一起孵育(激活)。淋巴细胞产生或激活MAF的能力不仅由致敏肿瘤细胞“触发”,也由正常细胞和带有致敏肿瘤细胞H-2决定簇的其他肿瘤细胞触发。用丝裂霉素-C处理淋巴细胞或用抗小鼠Ig和补体处理后,使巨噬细胞产生细胞毒性的能力并未降低。用抗T细胞血清或抗Thy 1.2血清及补体处理后,淋巴细胞的这种能力被消除。用抗Lyt 1或抗Lyt 2血清及补体处理后,激活能力显著降低,淋巴细胞产生MAF的能力被消除。将Lyt 1缺失和Lyt 2缺失的淋巴细胞混合,或将正常淋巴细胞加入Lyt 1缺失或Lyt 2缺失的细胞群中,均不能恢复产生MAF和激活的能力。这表明在这个同种异体系统中诱导巨噬细胞细胞毒性的淋巴细胞是Lyt-1+2+ T淋巴细胞,它们在发挥作用之前不需要分裂。