Hommel M, David P H, Guillotte M, Pereira da Silva L
Ann Immunol (Paris). 1982 Jan-Feb;133C(1):57-67. doi: 10.1016/0769-2625(82)90006-x.
Rodent malaria can be a useful experimental model for preliminary studies of some of the variables of a future malaria vaccine (e. g. optimal doses of merozoites to be used for immunization, nature of adjuvant, etc.). The present study shows that a partial protection can be achieved in outbred OF-1 mice after vaccination with isolated Plasmodium chabaudi merozoites and Freund's complete adjuvant. These results show the relative importance of parasite virulence, number of merozoites used for immunization and size of challenge inoculum. The optimal conditions for using such a model in vaccination experiments are discussed. In these conditions the major effect of immunization is to transform an acute lethal infection into an acute self-curing infection, which is subsequently followed by a solid state of protection against a secondary challenge.
啮齿动物疟疾可作为一种有用的实验模型,用于对未来疟疾疫苗的一些变量进行初步研究(例如用于免疫的裂殖子最佳剂量、佐剂的性质等)。本研究表明,在用分离的查巴迪疟原虫裂殖子和弗氏完全佐剂接种后,远交系OF-1小鼠可获得部分保护。这些结果表明了寄生虫毒力、用于免疫的裂殖子数量和攻击接种物大小的相对重要性。讨论了在疫苗接种实验中使用这种模型的最佳条件。在这些条件下,免疫的主要作用是将急性致死性感染转变为急性自愈性感染,随后产生针对二次攻击的稳固保护状态。