Bruinink A, Haller O
Exp Cell Biol. 1979;47(3):190-201.
Using M-TUR, a macrophage-adapted avian influenza A virus (Hav1, Nav3), antiviral resistance of peritoneal macrophages obtained from specifically or nonspecifically immunized mice towards in vitro infection was assessed. M-TUR grew to high titers in macrophages from nonimmune mice thereby causing a marked cytopathic effect. In contrast, peritoneal macrophages from mice specifically immunized with TUR virus were not affected by infection with M-TUR in vitro. This antiviral immunity was specific: mice immunized with antigenetically unrelated influenza strains such as influenza A/Hong Kong/1/68 (H3, N2) or influenza B/Lee yielded susceptible macrophages. Specific macrophage immunity could be abrogated by trypsin treatment in vitro. Susceptible macrophages from nonimmune hosts became resistant following in vitro exposure to homologous anti-TUR sera. Peritoneal exudate cells from BCG-infected animals were less susceptible to in vitro challenge with M-TUR than control macrophages. In vivo treatment of mice with the unspecific immunostimulants BCG or Corynebacterium parvum did not protect the animals against lethal infection with a hepatotropic variant of TUR.
利用M-TUR,一种适应巨噬细胞的甲型禽流感病毒(Hav1,Nav3),评估了从特异性或非特异性免疫小鼠获得的腹腔巨噬细胞对体外感染的抗病毒抗性。M-TUR在非免疫小鼠的巨噬细胞中生长至高滴度,从而引起明显的细胞病变效应。相比之下,用TUR病毒特异性免疫的小鼠的腹腔巨噬细胞在体外不受M-TUR感染的影响。这种抗病毒免疫是特异性的:用抗原性无关的流感毒株如甲型流感病毒/香港/1/68(H3,N2)或乙型流感病毒/李株免疫的小鼠产生易感巨噬细胞。特异性巨噬细胞免疫可通过体外胰蛋白酶处理消除。非免疫宿主的易感巨噬细胞在体外暴露于同源抗TUR血清后变得具有抗性。卡介苗感染动物的腹腔渗出细胞比对照巨噬细胞对M-TUR的体外攻击更不易感。用非特异性免疫刺激剂卡介苗或短小棒状杆菌对小鼠进行体内治疗并不能保护动物免受TUR嗜肝变体的致死性感染。