Feng Hui-min, Walker David H
Department of Pathology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555-0609, USA.
Vaccine. 2003 Sep 8;21(25-26):3901-5. doi: 10.1016/s0264-410x(03)00301-3.
Two excellent C3H/HeN mouse models of spotted fever rickettsioses caused by the distantly related organisms, Rickettsia conorii and Rickettsia australis, were utilized to evaluate the possibility of the stimulation of broad cross-protective immunity. Sublethal infection stimulated complete immunity, that is absence of disease, after challenge with a dose of the heterologous Rickettsia that uniformly killed naïve mice. In contrast, heterologous immune sera did not protect mice against a lethal dose (two LD50) of rickettsiae in the mouse toxicity neutralization assay, the standard method for evaluation of rickettsial vaccine potency. These observations suggest that development of a broadly protective vaccine against spotted fever group (SFG) rickettsiae is feasible, and the results indicate that mouse toxicity neutralization is an inappropriate method for evaluation of candidate vaccines.
利用两种优良的C3H/HeN小鼠模型来评估激发广泛交叉保护性免疫的可能性,这两种模型分别由远缘相关病原体——康氏立克次体和澳大利亚立克次体引起斑点热立克次体病。亚致死感染激发了完全免疫,即在使用能使未感染小鼠全部死亡的异源立克次体剂量进行攻击后不发病。相比之下,在评估立克次体疫苗效力的标准方法——小鼠毒性中和试验中,异源免疫血清不能保护小鼠免受致死剂量(两个半数致死量)立克次体的攻击。这些观察结果表明,开发一种针对斑点热群(SFG)立克次体的广泛保护性疫苗是可行的,结果还表明小鼠毒性中和是评估候选疫苗的不恰当方法。