Virgin H W, Unanue E R
J Immunol. 1984 Jul;133(1):104-9.
Murine infection with the facultative intracellular pathogen Listeria monocytogenes was studied as a model of cell-mediated immunity. Overwhelming lethal infection with Listeria developed when mice were given a secondary challenge with a protein antigen at the same time as Listeria infection. Three days after infection, mice immunized with ovalbumin and then challenged with Listeria and ovalbumin had up to 2.1(10)6 times as many viable Listeria organisms in their spleens as mice challenged only with Listeria. The suppressive effect of secondary challenge with a protein antigen was found to be antigen-specific, transient, and not dependent on route of challenge with either Listeria or ovalbumin. Secondary challenge with a protein antigen suppressed both the primary and the secondary responses to Listeria. Immune serum, or affinity-purified antibody, was found to transfer the suppressive effect to nonimmune mice. These findings demonstrate that acute formation of immune complexes causes a transient state of high susceptibility to infection with an intracellular pathogen. Possible mechanisms for, and implications of, these findings are discussed.
将兼性细胞内病原体单核细胞增生李斯特菌感染小鼠作为细胞介导免疫的模型进行了研究。当小鼠在感染李斯特菌的同时接受蛋白质抗原二次攻击时,会发生严重的致死性李斯特菌感染。感染三天后,用卵清蛋白免疫然后接受李斯特菌和卵清蛋白攻击的小鼠脾脏中存活的李斯特菌数量比仅接受李斯特菌攻击的小鼠多高达2.1×10⁶倍。发现蛋白质抗原二次攻击的抑制作用具有抗原特异性、短暂性,且不依赖于李斯特菌或卵清蛋白的攻击途径。蛋白质抗原二次攻击抑制了对李斯特菌的初次和二次反应。发现免疫血清或亲和纯化抗体可将抑制作用传递给未免疫的小鼠。这些发现表明,免疫复合物的急性形成会导致对细胞内病原体感染的高易感性短暂状态。讨论了这些发现的可能机制及其意义。