Antonissen A C, Lemmens P J, van den Bosch J F, van Boven C P
Immunol Lett. 1986 Nov 17;14(1):21-8. doi: 10.1016/0165-2478(86)90015-5.
In this study we investigated the mechanism of enhanced resistance against Listeria monocytogenes induced with Listeria ribosomal RNA and the adjuvant dimethyldioctadecylammonium bromide (DDA). Mice immunized with DDA alone (which were not protected against Listeria-infection) were used as negative controls. Mice immunized with RNA plus DDA were found to have an increased capacity to mobilize polymorphonuclear leukocytes (PMNs) and macrophages to the inflamed peritoneal cavity compared to mice immunized with adjuvant alone. Intraperitoneal (i.p.) inflammation was induced by injection of the sterile irritant proteose peptone. The protective capacity of various cell-populations was investigated by i.p. transfer of cells to normal recipient mice and concomitant challenge of recipient animals with a lethal dose of viable Listeria. Inflammatory PMNs as well as inflammatory macrophages from mice immunized with RNA plus DDA protected recipient animals against listeriosis whereas cells from mice immunized with DDA alone failed to do so. Therefore, enhanced mobilization as well as activation of PMNs and macrophages may have contributed to the expression of protection against L. monocytogenes induced with RNA plus DNA.
在本研究中,我们调查了用李斯特菌核糖体RNA和佐剂二甲基二十八烷基溴化铵(DDA)诱导产生的对单核细胞增生李斯特菌增强抵抗力的机制。单独用DDA免疫的小鼠(对李斯特菌感染无保护作用)用作阴性对照。与单独用佐剂免疫的小鼠相比,用RNA加DDA免疫的小鼠动员多形核白细胞(PMN)和巨噬细胞至炎症腹膜腔的能力增强。通过注射无菌刺激性蛋白胨诱导腹膜内(i.p.)炎症。通过将细胞i.p.转移至正常受体小鼠并同时用致死剂量的活李斯特菌攻击受体动物,研究了各种细胞群的保护能力。用RNA加DDA免疫的小鼠的炎性PMN以及炎性巨噬细胞保护受体动物免受李斯特菌病感染,而单独用DDA免疫的小鼠的细胞则不能。因此,PMN和巨噬细胞的增强动员以及激活可能有助于表达对RNA加DNA诱导的单核细胞增生李斯特菌的保护作用。