Shirahata T, Shimizu K, Suzuki N
Z Parasitenkd. 1976 Mar 31;49(1):11-23. doi: 10.1007/BF00445014.
In vitro studies on cell-mediated immunity against Toxoplasma infection were carried out by estimating the ability of antigenically stimulated lymphocytes. Splenic lymphocytes from normal mice and from hyper-immunized mice were cultured in the presence or absence of Toxoplasma lysate antigen. The cell-free supernatant fluids from the lymphocyte cultures were assassed for their ability to alter the functional capacities of normal macrophages. When glycogen-induced peritoneal macrophages were incubated with the culture supernatant from immune lymphocytes reacting with specific angigen, the intracellular multiplication of the organisms was inhibited remarkably. In contrast, the addition of antitoxoplasma antibody to culture medium had no effect on the enhancement of phagocytic activity of culture macrophages. However, when extra-cellular organisms were exposed to fresh or heat-inactivated immune serum just before infection of the monolayers, the intracellular multiplication of Toxoplasmas was inhibited significantly by either activated or normal macrophages.
通过评估抗原刺激淋巴细胞的能力,对细胞介导的抗弓形虫感染免疫进行了体外研究。将正常小鼠和超免疫小鼠的脾淋巴细胞在有无弓形虫裂解物抗原的情况下进行培养。对淋巴细胞培养物的无细胞上清液进行检测,以评估其改变正常巨噬细胞功能能力的能力。当糖原诱导的腹腔巨噬细胞与与特异性抗原反应的免疫淋巴细胞的培养上清液一起孵育时,病原体的细胞内增殖受到显著抑制。相比之下,向培养基中添加抗弓形虫抗体对培养巨噬细胞吞噬活性的增强没有影响。然而,当细胞外病原体在感染单层细胞之前暴露于新鲜或热灭活的免疫血清时,活化或正常巨噬细胞均能显著抑制弓形虫的细胞内增殖。