Van Der Meer C, Hofhuis F M, Willers J M
Immunology. 1979 May;37(1):77-82.
Delayed-type hypersensitivity (DH) and acquired cellular resistance (ARC) to Listeria monocytogenes in mice was studied following immunization with killed bacteria in combination with Freund's complete adjuvant or the adjuvant dimethyldioctadecylammonium bromide (DDA). Intracutaneous or intraperitoneal injections of killed listeria mixed with Freund's complete adjuvant did neither result in DH nor in ACR. Intracutaneous injections of killed listeria and DDA resulted in an antigen-dose dependent DH but not in ACR. Intraperitoneal injections of listeria and DDA, however, induced ACR but no DH. Optimal conditions for the induction of ACR were simultaneous intraperitoneal injection of 15 mg DDA/kg body weight and 10(7) or 10(8) listeria. The optimal interval between immunization and challenge was 7 days. No protection was found against challenge with a lethal dose of Salmonella enteritidis, suggesting that the protection is specific. Intraperitoneal injection of mice with DDA resulted in inhibition of phagosome-lysosome fusion in macrophages harvested 24 h later. Interference with macrophage activity is discussed as one of the possible mechanisms for the adjuvant effect of DDA.
在用灭活细菌与弗氏完全佐剂或二甲基二十八烷基溴化铵(DDA)佐剂联合免疫小鼠后,研究了小鼠对单核细胞增生李斯特菌的迟发型超敏反应(DH)和获得性细胞抗性(ARC)。皮内或腹腔注射与弗氏完全佐剂混合的灭活李斯特菌,既未导致DH,也未导致ACR。皮内注射灭活李斯特菌和DDA可导致抗原剂量依赖性DH,但不会导致ACR。然而,腹腔注射李斯特菌和DDA可诱导ACR,但不会导致DH。诱导ACR的最佳条件是同时腹腔注射15 mg DDA/ kg体重和10⁷或10⁸个李斯特菌。免疫和攻击之间的最佳间隔为7天。未发现对致死剂量肠炎沙门氏菌攻击的保护作用,这表明这种保护是特异性的。给小鼠腹腔注射DDA会导致24小时后收获的巨噬细胞中吞噬体-溶酶体融合受到抑制。干扰巨噬细胞活性被认为是DDA佐剂效应的可能机制之一。