Sethi K K, Pelster B, Suzuki N, Piekarski G, Brandis H
J Immunol. 1975 Oct;115(4):1151-8.
Male and female CBA mice were used to study in vitro the mechanisms involved in the development and expression of cellular immunity to toxoplasma infection. The lag phase preceding toxoplasma division was delayed in nonimmune macrophages obtained from peritoneal cavities stimulated with thioglycollate. Specific anti-toxoplasma activity was conferred on nonimmune macrophages incubated with toxoplasma-immune spleen lymphocytes and soluble toxoplasma antigen. Treatment of immune spleen cell populations with anti-theta serum plus complement abolished completely their activity of conferring anti-toxoplasma activity on nonimmune macrophages, demonstrating that the essential cells were T lymphocytes. The mediator(s) responsible for the acquisition of immunity to toxoplasma in the nonimmune macrophages were soluble. Heat-inactivated, toxoplasm-immune macrophages of fibroblasts. The findings are related to previous investigations of induced immunity in animals and man.
采用雄性和雌性CBA小鼠在体外研究细胞免疫对弓形虫感染的发生和表达机制。在用巯基乙酸刺激的腹腔获得的非免疫巨噬细胞中,弓形虫分裂前的延迟期被延长。将非免疫巨噬细胞与弓形虫免疫脾淋巴细胞及可溶性弓形虫抗原一起孵育,可赋予其特异性抗弓形虫活性。用抗θ血清加补体处理免疫脾细胞群体,可完全消除它们赋予非免疫巨噬细胞抗弓形虫活性的能力,表明关键细胞是T淋巴细胞。负责使非免疫巨噬细胞获得对弓形虫免疫力的介质是可溶性的。热灭活的弓形虫免疫巨噬细胞或成纤维细胞。这些发现与先前对动物和人类诱导免疫的研究相关。