特殊活化巨噬细胞活疫苗对肠炎沙门氏菌的氧不依赖性抗菌活性研究。

T Sasahara, N Ikewaki, H Tamauchi, N Osawa
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引用次数: 0

摘要

比较了肠沙门氏菌SER和Jena两种减毒株感染小鼠后腹腔巨噬细胞的特征。用SER菌株免疫的小鼠对肠炎沙门氏菌强毒株116-54有较强的抵抗力,而用耶拿菌株免疫的小鼠和对照组没有较强的抵抗力。与Jena和TG诱导的巨噬细胞相比,SER免疫小鼠腹腔巨噬细胞在感染后7至14天显示出更强的沙门氏菌杀灭活性,O2-的产生增加,Ia抗原的表达增加。感染第4天后,Jena菌株在脏器内的细菌数量比SER菌株减少得更快。这些观察结果表明,减毒沙门氏菌杆菌在网状内皮中的存活对其巨噬细胞活性的增加至关重要。小鼠巨噬细胞注射重组干扰素(IFN)- γ 3天后诱导的活化阶段与SER菌株免疫小鼠的活化阶段具有相同的特征。氧中间体(OI)清除剂如超氧化物歧化酶和过氧化氢酶对活化巨噬细胞的沙门氏菌杀灭活性的影响完全没有观察到。这些结果表明,在用活的、减毒的菌株免疫和注射rifn - γ激活的巨噬细胞中,OI的增加可能不是抑制肠炎沙门氏菌毒力菌株细胞内生长的主要原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oxygen-independent antimicrobial activity against Salmonella enteritidis of specially activated macrophage with living vaccine.

Characteristics of peritoneal macrophages recovered from mice infected with two attenuated strains SER and Jena of Salmonella enteritidis were compared. Strong resistance against lethal infection with a virulent strain 116-54 of S. enteritidis was seen in a group of mice immunized with strain SER, but not in a group of mice immunized with strain Jena as well as in a control group. Peritoneal macrophages from mice immunized with strain SER showed an enhanced Salmonella-killing activity, an increased generation of O2- and an increased expression of Ia antigen on 7 to 14 days after infection when compared with those from mice immunized with strain Jena and thioglycollate(TG)-elicited macrophages as a control. The bacterial number of strain Jena in organs decreased more rapidly than that of strain SER after day 4 of infection. These observations suggest that the survival of an attenuated Salmonella bacilli at reticulo-endothelium is essential to increase of their activities of macrophages. Macrophages from mice injected with recombinant interferon(IFN)-gamma for 3 days induced the activated stage of the same characteristics as noted in activated macrophages from mice immunized with strain SER. Effect of oxygen intermediates (OI) scavengers such as superoxide dismutase and catalase on Salmonella-killing activity of activated macrophages was not seen at all. These results suggest that an increased generation of OI may be not primarily responsible for the ability to inhibit the intracellular growth of a virulent strain of S. enteritidis in macrophages activated by immunization with live, attenuated strains and injection with rIFN-gamma.

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