Hauser T, Frei K, Zinkernagel R M, Leist T P
Laboratory of Experimental Pathology, University Hospital Zurich, Switzerland.
Med Microbiol Immunol. 1990;179(2):95-104. doi: 10.1007/BF00198530.
The effects of sheep anti-murine recombinant tumor necrosis factor-alpha (TNF-alpha) on resistance to Listeria monocytogenes infection were studied in T cell-deficient nu/nu mice. The sheep anti-TNF-alpha antibody preparation was specific for TNF since it neutralized 300 U of recombinant murine TNF-alpha in vitro at a dilution of up to 1/1,000 but did not neutralize 32 U of interferon (IFN)-alpha, -beta or 32 U of IFN-gamma in vitro at a 1/20 dilution. When tested in vivo in sublethally Listeria-infected nu/nu or T cell-competent C57BL/6 or ICR mice, a single treatment of 0.2 ml anti-TNF-alpha given intraperitoneally on either day -1,0 or +1 resulted in the death of mice by day 5-7 due to the uncontrolled growth of Listeria; bacterial counts in spleen and liver were increased on days 3-5 by a factor of 10-1,000 in these organs. When examined histologically, organs from mice with the anti-TNF-alpha treatment contained more, and considerably bigger, lesions that exhibited central necrosis. The enhancing effect of anti-TNF-alpha on Listeria infection seemed greater early during Listeria infection on days 1-6 when compared to later phases of the infection around days 6-10. From the data presented we conclude that in addition to other lymphokines, such as IFN-gamma, TNF-alpha is of importance during the entire course of a Listeria infection in nu/nu mice.
在T细胞缺陷的裸鼠中研究了羊抗小鼠重组肿瘤坏死因子-α(TNF-α)对单核细胞增生李斯特菌感染抵抗力的影响。羊抗TNF-α抗体制剂对TNF具有特异性,因为它在体外以高达1/1000的稀释度可中和300 U的重组小鼠TNF-α,但在1/20的稀释度下不能在体外中和32 U的干扰素(IFN)-α、-β或32 U的IFN-γ。当在亚致死剂量感染李斯特菌的裸鼠或具有T细胞功能的C57BL/6或ICR小鼠体内进行测试时,在第-1、0或+1天腹腔内单次注射0.2 ml抗TNF-α会导致小鼠在第5-7天死亡,原因是李斯特菌不受控制地生长;在这些器官中,脾脏和肝脏中的细菌计数在第3-5天增加了10-1000倍。组织学检查时,接受抗TNF-α治疗的小鼠器官中含有更多且明显更大的病变,表现为中央坏死。与感染后期第6-10天相比,抗TNF-α对李斯特菌感染的增强作用在感染早期第1-6天似乎更大。根据所呈现的数据,我们得出结论,除了其他淋巴因子,如IFN-γ外,TNF-α在裸鼠李斯特菌感染的整个过程中也很重要。