Brunner H, Feldner J, Bredt W
Isr J Med Sci. 1984 Sep;20(9):878-81.
Mycoplasma pneumoniae, an important human pathogen, is an extra-cellular parasite, colonizing mucosal surfaces. Attachment to epithelial cells of the host is therefore an important mechanism of pathogenicity, and inhibition of adhesion might protect the host. M. pneumoniae predominantly adheres with a special organelle, the attachment-tip, to host cells. In vitro studies confirmed the observation that monoclonal antibodies (MOAB) to the tip inhibited adherence to erythrocytes. In animal experiments, high numbers of virulent M. pneumoniae exposed for 4 h at 37 C to MOAB and kept in suspension with MOAB 1:100 were inoculated intranasally into hamsters. A significant reduction in the lung lesion score, but not in the numbers of organisms in lung tissue or wash fluid of the upper respiratory tract, was seen in hamsters 14 days after inoculation of MOAB-treated organisms, as compared with controls. These observations, although preliminary, may have implications for the understanding of pathogenesis and for vaccine development.
肺炎支原体是一种重要的人类病原体,是一种胞外寄生虫,定殖于粘膜表面。因此,附着于宿主上皮细胞是一种重要的致病机制,而抑制粘附可能会保护宿主。肺炎支原体主要通过一种特殊的细胞器——附着尖端与宿主细胞粘附。体外研究证实了针对该尖端的单克隆抗体(MOAB)可抑制与红细胞的粘附这一观察结果。在动物实验中,将大量在37℃下暴露于MOAB 4小时并与MOAB以1:100比例悬浮保存的强毒肺炎支原体经鼻接种到仓鼠体内。与对照组相比,在接种经MOAB处理的病原体14天后的仓鼠中,肺部病变评分显著降低,但肺组织或上呼吸道冲洗液中的病原体数量并未减少。这些观察结果尽管是初步的,但可能对理解发病机制和疫苗开发具有启示意义。