Toder V, Blank M, Nebel L
Br J Exp Pathol. 1977 Dec;58(6):678-82.
The lymph node and spleen lymphocytes of placenta-sensitized guinea pigs were tested for their ability to destroy kidney monolayer. It was shown by microcytotoxicity assay that these sensitized lymphoid cells killed target monolayer at different effector/target cell ratios. About 35% of kidney cells were destroyed when sensitized lymph node cells were added at a ratio of 500: 1, and 50% at a ratio of 1000:1. Immunized spleen cells produced approximately the same results. No significant cytotoxicity was measured when placenta-sensitized lymphocytes were added to nonrelated mouse skin fibroblasts. In order to exclude the possibility of participation of species-specific antigens in this experimental model, placenta-sensitized lymphocytes were added to L-cell monolayer in the presence of kidney antigens or mouse normal serum (a carrier of species-specific determinants). An extensive cytotoxic effect was observed in the presence of kidney antigens, while addition of mouse normal serum did not induce significant target cell lysis. The cross-reactivity of the cytotoxic ability of placenta-sensitized lymphocytes may indicate that cell-mediated immunity can be involved in the pathogenesis of nephropathy in toxaemic pregnancies, accompanying sensitization by placental antigens.
对经胎盘致敏的豚鼠的淋巴结和脾脏淋巴细胞进行检测,以评估它们破坏肾单层细胞的能力。微细胞毒性试验表明,这些致敏淋巴细胞在不同的效应细胞/靶细胞比例下能够杀死靶单层细胞。当以500:1的比例加入致敏淋巴结细胞时,约35%的肾细胞被破坏;当比例为1000:1时,50%的肾细胞被破坏。免疫后的脾细胞产生了大致相同的结果。当将经胎盘致敏的淋巴细胞加入到无关的小鼠皮肤成纤维细胞中时,未检测到明显的细胞毒性。为了排除物种特异性抗原参与该实验模型的可能性,在存在肾抗原或小鼠正常血清(物种特异性决定簇的载体)的情况下,将经胎盘致敏的淋巴细胞加入到L细胞单层中。在存在肾抗原的情况下观察到广泛的细胞毒性作用,而加入小鼠正常血清并未诱导明显的靶细胞裂解。经胎盘致敏淋巴细胞细胞毒性能力的交叉反应性可能表明,细胞介导的免疫可能参与了中毒性妊娠肾病的发病机制,并伴随着胎盘抗原致敏。