Alexander J E, Lock R A, Peeters C C, Poolman J T, Andrew P W, Mitchell T J, Hansman D, Paton J C
Department of Microbiology and Immunology, University of Leicester, United Kingdom.
Infect Immun. 1994 Dec;62(12):5683-8. doi: 10.1128/iai.62.12.5683-5688.1994.
Pneumolysin is the thiol-activated cytolysin produced by Streptococcus pneumoniae. Mice were immunized with a genetically engineered toxoid version of pneumolysin, which was derived from a serotype 2 pneumococcus. The toxoid carried the mutation Trp-433-->Phe. Alum was used as the adjuvant. Immunized mice had significantly increased levels of anti-pneumolysin antibodies, principally immunoglobulin G1. Mice were challenged intraperitoneally or intranasally with 12 strains covering capsular serotypes 1 to 6, 7F, 8, and 18C. Following challenge, the survival rate and/or the time of death of nonsurvivors (survival time) was significantly greater than that of sham-immunized mice for all nine serotypes. However, differences in the degree of protection were noted between different strains. The route of challenge also appeared to influence the degree of protection. Nevertheless, the significant, albeit in some cases partial, protection provided against all nine pneumococcal serotypes supports the conclusion that pneumolysin toxoids warrant consideration for inclusion in a human vaccine.
肺炎溶血素是肺炎链球菌产生的硫醇激活细胞毒素。用源自2型肺炎球菌的基因工程类毒素形式的肺炎溶血素免疫小鼠。该类毒素携带Trp-433→Phe突变。使用明矾作为佐剂。免疫小鼠的抗肺炎溶血素抗体水平显著升高,主要是免疫球蛋白G1。用覆盖1至6、7F、8和18C荚膜血清型的12种菌株对小鼠进行腹腔内或鼻内攻击。攻击后,对于所有九种血清型,非存活小鼠的存活率和/或死亡时间(存活时间)显著高于假免疫小鼠。然而,不同菌株之间在保护程度上存在差异。攻击途径似乎也会影响保护程度。尽管如此,针对所有九种肺炎球菌血清型提供的显著保护(尽管在某些情况下是部分保护)支持了肺炎溶血素类毒素值得考虑纳入人类疫苗的结论。