Collins F M, Montalbine V
Am Rev Respir Dis. 1975 Jan;111(1):43-51. doi: 10.1164/arrd.1975.111.1.43.
Normal CD-1 mice were infected intravenously, subcutaneously, or aerogenically with live bacille Calmette Guerin (BCG) Tice or BCG streptomycin resistant (SM-res) and growth of the organisms in the footpad, the draining popliteal lymph node, the blood, lung, liver, and spleen was followed for as long as 50 days. The vaccinated mice were then challenged on day 50 with 10-5 viable Mycobacterium tuberculosis Erdman organisms introduced intravenously or subcutaneously. The growth of the Erdman challenge was followed in the appropriate organs for the next 20 days. Measurement of tuberculin hypersensitivity was carried out by footpad tests. The BCG Tice introduced aerogenically or subcutaniously into normal mice induced degrees of antituberculous resistance equivalent to those seen earlier in intravenously infected mice. The BCG SM-res was still nonimmunogenic when introduced subcutaneously or by the aerogenic route. Suspension of the organisms in sterile mineral oil before their injection into the footpad slowed their rate of inactivation and marginally increased the immune response seen later in the host. Introduction of BCG SM-res into T-cell depleted mice by the 3 inoculation routes was associated with no marked improvement in the survival of this organism in vivo, suggesting that BCG SM-res is inactivated in vivo by a nonimmunologically mediated mechanism.
将活的卡介苗(BCG)Tice株或耐链霉素卡介苗(BCG SM-res)通过静脉、皮下或气溶胶途径感染正常CD-1小鼠,并观察长达50天的时间里,这些细菌在足垫、引流的腘淋巴结、血液、肺、肝和脾中的生长情况。然后在第50天,对接种过疫苗的小鼠通过静脉或皮下途径注射10-5个存活的结核分枝杆菌 Erdman株进行攻击。在接下来的20天里,观察Erdman攻击株在相应器官中的生长情况。通过足垫试验进行结核菌素超敏反应的检测。通过气溶胶或皮下途径将BCG Tice引入正常小鼠所诱导的抗结核抵抗力程度,与之前静脉感染小鼠中观察到的相当。当通过皮下或气溶胶途径引入时,BCG SM-res仍然没有免疫原性。在将细菌注射到足垫之前,将其悬浮于无菌矿物油中会减缓其失活速度,并在一定程度上增强宿主随后出现的免疫反应。通过三种接种途径将BCG SM-res引入T细胞耗竭的小鼠体内,并未使其在体内的存活情况有明显改善,这表明BCG SM-res在体内是通过非免疫介导机制失活的。