Berche P, Gaillard J L, Sansonetti P J
J Immunol. 1987 Apr 1;138(7):2266-71.
The in vivo induction of T cell-mediated immunity was studied by infecting mice with two genetically closely related mutants from Listeria monocytogenes, differing only with respect to the secretion of an active SH-dependent hemolysin. It is shown that even minute doses of hemolytic bacteria capable of growing in host tissues easily induced the expression of T cell-mediated immunity, as estimated by the level of delayed sensitivity, adoptive protection and long-lasting immunological memory. On the contrary, nonhemolytic bacteria unable to multiply in host tissues totally failed to initiate the expression of T cell-mediated immunity in vivo. This failure was even observed when mice were repeatedly infected by high doses of nonhemolytic bacteria, allowing to maintain a significant amount of viable bacteria for several days in host tissues. These results mean that the presence of viable bacteria at a significant level in the host is not sufficient per se to induce detectable T cell clonal expansion in the in vivo setting, implying that the process of bacterial growth inside macrophages is required to initiate in vivo the expression of T cell-mediated immunity.
通过用来自单核细胞增生李斯特菌的两个遗传关系密切的突变体感染小鼠,研究了体内T细胞介导免疫的诱导情况,这两个突变体仅在活性SH依赖性溶血素的分泌方面有所不同。结果表明,即使是能够在宿主组织中生长的微量溶血性细菌,也很容易诱导T细胞介导免疫的表达,这可以通过迟发型超敏反应水平、过继性保护和持久免疫记忆来评估。相反,无法在宿主组织中繁殖的非溶血性细菌完全无法在体内启动T细胞介导免疫的表达。即使小鼠被高剂量的非溶血性细菌反复感染,使得宿主组织中在数天内维持大量活菌,这种失败情况仍会出现。这些结果意味着,宿主中存在大量活菌本身不足以在体内诱导可检测到的T细胞克隆扩增,这意味着巨噬细胞内的细菌生长过程是在体内启动T细胞介导免疫表达所必需的。