Schechter B, Segal S, Feldman M
J Immunol. 1978 Apr;120(4):1268-73.
We investigated the effect of depletion of histamine-binding lymphoid cells on immunological properties of lymphocytes sensitized in culture against tumor cells. C57BL/6 spleen cells that were sensitized in vitro on monolayers of the syngeneic Lewis lung carcinoma (3LL) became cytotoxic to the tumor cells in vitro after 3 to 5 days of sensitization. Sensitized cells harvested after 4 days of sensitization occasionally enhanced tumor growth in vivo. Fractionation of the sensitized lymphocytes over insolubilized histamine-rabbit serum albumin-Sepharose (HRS) columns decreased or abolished the enhancing activity in vivo and specifically increased the in vitro cytotoxic activity of the depleted lymphocytes. A similar increase in the cytotoxic activity of HRS-fractionated cells was observed in an allogeneic combination of C57BL spleen cells sensitized against C3H fibroblasts. The effect of HRS chromatography on the in vitro cytotoxic activity increased with prolonged incubation of the depleted effector cells with the target cells.
我们研究了组胺结合淋巴细胞耗竭对体外培养致敏于肿瘤细胞的淋巴细胞免疫特性的影响。在同基因Lewis肺癌(3LL)单层细胞上体外致敏的C57BL/6脾细胞,致敏3至5天后在体外对肿瘤细胞产生细胞毒性。致敏4天后收获的致敏细胞偶尔会在体内促进肿瘤生长。将致敏淋巴细胞通过不溶性组胺-兔血清白蛋白-琼脂糖(HRS)柱进行分离,可降低或消除体内的增强活性,并特异性增加耗竭淋巴细胞的体外细胞毒性活性。在针对C3H成纤维细胞致敏的C57BL脾细胞的同种异体组合中,观察到HRS分离的细胞的细胞毒性活性有类似增加。HRS层析对体外细胞毒性活性的影响随着耗竭的效应细胞与靶细胞孵育时间的延长而增加。