Effects of Staphylococcus epidermidis on Cellular Immunity to Infection with Listeria monocytogenes

Stefan Ehlers , Arne C. Rodloff , Helmut Hahn
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引用次数: 4

Abstract

With the present study, the effects of intravenous applications of Staphylococcus epidermidis (SE) on the course of experimental infections of mice with Listeria monocytogenes were evaluated. SE treatment 24 h prior to Listeria infection led to a reduced growth of Listeria organisms in both livers and spleens and to an increased resistance of infected animals against a lethal Listeria challenge. SE treatment 24 h after Listeria infection resulted in an enhanced growth of and retarded elimination of Listeria organisms from animal organs as well as in a reduction of delayed-type hypersensitivity to soluble Listeria antigen. Adoptive immunotherapy accomplished by transferring immune peritoneal exudate T-lymphocyte-enriched cells (PETLEs) to Listeria-infected recipients 24 h before SE treatment did not prevent the delay in clearance of Listeria organisms. When Listeria-infected recipients compromised in their immune response by SE treatment were infused with immune PETLEs either immediately or 24 h after the application of SE, the immunosuppression induced by SE proved to be reversible. It is concluded that, in analogy to other bacterial immunomodulators, Staphylococcus epidermidis is able to either nonspecifically activate macrophages or interfere with T-lymphocyte functions.

表皮葡萄球菌对单核增生李斯特菌感染细胞免疫的影响
本研究评价了表皮葡萄球菌(SE)静脉注射对小鼠实验性单核细胞增生李斯特菌感染过程的影响。在李斯特菌感染前24小时进行SE治疗,可减少肝脏和脾脏中李斯特菌的生长,并增强受感染动物对致命李斯特菌攻击的抵抗力。李斯特菌感染24小时后,SE处理导致动物器官中李斯特菌的生长增强和消除迟缓,以及对可溶性李斯特菌抗原的延迟型超敏反应减少。通过在SE治疗前24小时将免疫的腹膜渗出t淋巴细胞富集细胞(PETLEs)转移给李斯特菌感染的受者来完成过继免疫治疗,并不能阻止李斯特菌有机体清除的延迟。当李斯特菌感染的免疫反应受损的受者在使用SE后立即或24小时内输注免疫PETLEs时,SE诱导的免疫抑制被证明是可逆的。由此可见,与其他细菌免疫调节剂类似,表皮葡萄球菌能够非特异性激活巨噬细胞或干扰t淋巴细胞功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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