Stanley H A, Reese R T
Am J Trop Med Hyg. 1984 Jan;33(1):12-6. doi: 10.4269/ajtmh.1984.33.12.
Beginning at the ring stage, synchronized cultures of Plasmodium falciparum were grown in suspension for 22-32 hours. Intracellular growth was assayed by measuring cellular uptake and incorporation into protein of 35S-methionine. Low concentrations (2%) of serum from immune humans and Aotus monkeys were found to inhibit the uptake of the 35S-methionine. The amount of inhibition for a given serum was often inversely related to its indirect fluorescent antibody test titer. Inhibition occurred during the trophozoite stage and was not obtained with a clone lacking the erythrocyte modifications referred to as knobs. Thus, a sensitive new assay is described which allows detection of factors in immune primate sera which can affect maturation of P. falciparum within the erythrocyte. These serum factors are likely to be antibodies which react with antigens expressed at the trophozoite stage on the surface of K+-infected erythrocytes.
从环状体阶段开始,恶性疟原虫的同步培养物在悬浮液中培养22 - 32小时。通过测量35S - 甲硫氨酸的细胞摄取量及其掺入蛋白质的量来检测细胞内生长情况。发现来自免疫人群和夜猴的低浓度(2%)血清可抑制35S - 甲硫氨酸的摄取。给定血清的抑制量通常与其间接荧光抗体试验效价呈负相关。抑制发生在滋养体阶段,而缺乏称为“隆起”的红细胞修饰的克隆则未出现这种抑制现象。因此,描述了一种灵敏的新检测方法,该方法能够检测免疫灵长类动物血清中可影响红细胞内恶性疟原虫成熟的因子。这些血清因子可能是与K +感染红细胞表面滋养体阶段表达的抗原发生反应的抗体。