Kaufmann S H
Abt. Med. Mikrobiol. Immunol., Oberer Eselsberg, Ulm.
Infection. 1988;16 Suppl 2:S128-36. doi: 10.1007/BF01639735.
Evidence is summarized to suggest that both CD4 and CD8 T cells and both helper and cytolytic T cell functions are involved in protective immunity to infection with the intracellular bacterium, Listeria monocytogenes. This suggestion is based on the following findings obtained with T cell lines and clones from L. monocytogenes infected mice: L3T4+ (CD4) T cells produce multiple lymphokines after antigen stimulation in vitro; Lyt2+ (CD8) T cells lyse L. monocytogenes primed macrophages; L3T4+ (CD4) T cells also lyse L. monocytogenes primed macrophages provided the latter express Ia-molecules; Lyt2+ (CD8) T cells secret Interferon-gamma provided that exogenous Interleukin-2 is supplied. Furthermore, both L3T4+ (CD4) and Lyt2+ (CD8) T cell lines can confer a certain degree of adoptive protection upon naive recipient mice.
现有证据表明,CD4和CD8 T细胞以及辅助性和细胞溶解性T细胞功能均参与了针对细胞内细菌——单核细胞增生李斯特菌感染的保护性免疫。这一观点基于从感染单核细胞增生李斯特菌的小鼠中获得的T细胞系和克隆所得到的以下发现:L3T4 +(CD4)T细胞在体外受到抗原刺激后会产生多种淋巴因子;Lyt2 +(CD8)T细胞可裂解经单核细胞增生李斯特菌致敏的巨噬细胞;只要L3T4 +(CD4)T细胞致敏的巨噬细胞表达Ia分子,L3T4 +(CD4)T细胞也可裂解这些巨噬细胞;只要提供外源性白细胞介素-2,Lyt2 +(CD8)T细胞就会分泌γ-干扰素。此外,L3T4 +(CD4)和Lyt2 +(CD8)T细胞系均可给予未接触过抗原的受体小鼠一定程度的过继性保护。