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补体在小鼠实验性肺炎球菌肺炎发展中的保护作用。

Protective role of complement in the development of experimental pneumococcal pneumonia in mice.

作者信息

Nakajima R, Namba K, Ishida Y, Une T, Osada Y

机构信息

Research Institute, Daiichi Pharmaceutical Co., Ltd., Tokyo, Japan.

出版信息

Chemotherapy. 1990;36(4):287-93. doi: 10.1159/000238779.

Abstract

To evaluate the role of complement in the lung defense against Streptococcus pneumoniae, mice decomplemented with multiple injections of cobra venom factor were challenged with type 3 pneumococci by inhalation. Without injection of cobra venom factor, the organisms were eliminated rapidly from the lungs in the majority of mice, accompanied by a significant but transient decrease in the serum C3 level. Focal pneumonia developed occasionally in some mice retaining the organisms in the lungs. By decomplementation with cobra venom factor, on the other hand, pneumococci were not eliminated completely from the lungs during the early stage of infection and afterward proliferated extensively. Consequently, the mice developed typical pneumococcal pneumonia with attendant bacteremia, while the serum C3 level has recovered compensatory during the course of infection. Thus, the complement was indicated to play an important role in the lung defense against pneumococci in mice, especially during the early stage of infection.

摘要

为评估补体在肺部抵御肺炎链球菌中的作用,通过多次注射眼镜蛇毒因子使小鼠失活补体,然后经吸入途径用3型肺炎球菌对其进行攻击。未注射眼镜蛇毒因子时,大多数小鼠肺部的细菌能迅速被清除,同时血清C3水平显著但短暂下降。部分肺部留存细菌的小鼠偶尔会发生局灶性肺炎。另一方面,通过眼镜蛇毒因子使补体失活后,肺炎球菌在感染早期未从肺部完全清除,随后大量增殖。结果,小鼠发展为典型的肺炎球菌性肺炎并伴有菌血症,而血清C3水平在感染过程中已代偿性恢复。因此,表明补体在小鼠肺部抵御肺炎球菌中发挥重要作用,尤其是在感染早期。

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