Adams J, Follett D, Hamilton H, Czuprynski C
Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison.
Immunol Lett. 1993 Feb;35(2):183-9. doi: 10.1016/0165-2478(93)90089-k.
In this study, we examined the roles of CD4+ and CD8+ cells in resistance to experimental paratuberculosis. Mice received purified anti-CD4 or anti-CD8 monoclonal antibodies before intragastric challenge with Mycobacterium paratuberculosis and on a biweekly basis for six months. This resulted in sustained depletion of CD4+ and CD8+ cells as verified by flow cytometry analysis of spleen cells from M. paratuberculosis infected mice. Depletion of CD4+ or CD8+ cells did not enhance fecal shedding of M. paratuberculosis, bacillary multiplication in the liver and ceca, nor histopathologic damage to the intestinal tract, mesenteric lymph nodes, spleen and liver. These data suggest that cells other than CD4+ or CD8+ cells are important for host defense in experimental paratuberculosis.
在本研究中,我们检测了CD4+和CD8+细胞在实验性副结核病抗性中的作用。小鼠在经副结核分枝杆菌进行胃内攻击之前接受纯化的抗CD4或抗CD8单克隆抗体,并每两周一次,持续六个月。通过对感染副结核分枝杆菌小鼠的脾细胞进行流式细胞术分析证实,这导致CD4+和CD8+细胞持续耗竭。CD4+或CD8+细胞的耗竭并未增强副结核分枝杆菌的粪便排出量、肝脏和盲肠中的细菌增殖,也未增强肠道、肠系膜淋巴结、脾脏和肝脏的组织病理学损伤。这些数据表明,除CD4+或CD8+细胞之外的其他细胞对于实验性副结核病中的宿主防御很重要。