Yamamoto K, Kato K, Kimura T
Immunology. 1985 Aug;55(4):609-19.
Pretreatment of mice by intravenous injection with killed Listeria provided neither delayed-type hypersensitivity to Listeria protoplasm nor protection against Listeria infection. Assuming that this suppression is due to suppressor cells, we attempted to clarify their induction and characterization. Pretreatment with killed BCG instead of killed Listeria suppressed the induction of DTH and protection in subsequent Listeria-immunized mice. Conversely, pretreatment with killed Listeria suppressed subsequent induction of DTH to PPD or protection from tuberculosis. Thus, these suppressions were induced antigen nonspecifically. Transfer of splenic non-adherent cells from killed Listeria-injected mice which had been treated with anti-BA theta serum plus complement, or had been passed through Sephadex G-10 columns, resulted in both afferent and efferent DTH suppression, suggesting that the DTH suppression is closely associated with suppressor T cells. Moreover, the splenic nonadherent cells from killed Listeria-injected mice showed suppression in vitro of listericidal activity of PEC from Listeria-immune mice in the presence of Listeria protoplasm.
通过静脉注射灭活李斯特菌对小鼠进行预处理,既未产生对李斯特菌原生质的迟发型超敏反应,也未提供针对李斯特菌感染的保护作用。假设这种抑制作用是由抑制性细胞引起的,我们试图阐明它们的诱导过程和特性。用灭活卡介苗而非灭活李斯特菌进行预处理,可抑制后续接种李斯特菌的小鼠中迟发型超敏反应的诱导和保护作用。相反,用灭活李斯特菌进行预处理可抑制后续对结核菌素纯蛋白衍生物的迟发型超敏反应的诱导或对结核病的保护作用。因此,这些抑制作用是由抗原非特异性诱导的。将来自注射过灭活李斯特菌的小鼠的脾非黏附细胞进行转移,这些小鼠已用抗BAθ血清加补体处理过,或已通过葡聚糖凝胶G - 10柱,结果导致传入和传出迟发型超敏反应均受到抑制,这表明迟发型超敏反应的抑制与抑制性T细胞密切相关。此外,来自注射过灭活李斯特菌的小鼠的脾非黏附细胞在存在李斯特菌原生质的情况下,体外可抑制来自李斯特菌免疫小鼠的腹腔渗出细胞的杀菌活性。