Bosarge J R, Watt J M, McDaniel D O, Swiatlo E, McDaniel L S
Department of Microbiology, The University of Mississippi Medical Center, Jackson, Mississippi 39216, USA.
Infect Immun. 2001 Sep;69(9):5456-63. doi: 10.1128/IAI.69.9.5456-5463.2001.
Pneumococcal surface protein A (PspA) is a pneumococcal virulence factor capable of eliciting protection against pneumococcal infection in mice. Previous studies have demonstrated that the protection is antibody mediated. Here we examined the ability of pspA to elicit a protective immune response following genetic immunization of mice. Mice were immunized by intramuscular injections with a eukaryotic expression vector encoding the alpha-helical domain of PspA/Rx1. Immunization induced a PspA-specific serum antibody response, and immunized mice survived pneumococcal challenge. Survival and antibody responses occurred in a dose-dependent manner, the highest survival rates being seen with doses of 10 microg or greater. The ability of genetic immunization to elicit cross-protection was demonstrated by the survival of immunized mice challenged with pneumococcal strains differing in capsule and PspA types. Also, immunized mice were protected from intravenous and intratracheal challenges with pneumococci. Similar to the results seen with immunization with PspA, the survival of mice genetically immunized with pspA was antibody mediated. There was no decline in the level of protection 7 months after immunization. These results support the use of genetic immunization to elicit protective immune responses against extracellular pathogens.
肺炎球菌表面蛋白A(PspA)是一种肺炎球菌毒力因子,能够在小鼠中引发针对肺炎球菌感染的保护作用。先前的研究表明,这种保护作用是由抗体介导的。在此,我们研究了pspA在小鼠基因免疫后引发保护性免疫反应的能力。通过肌肉注射用编码PspA/Rx1α螺旋结构域的真核表达载体对小鼠进行免疫。免疫诱导了PspA特异性血清抗体反应,且免疫小鼠在肺炎球菌攻击后存活。存活和抗体反应呈剂量依赖性,剂量为10微克或更高时观察到最高存活率。用不同荚膜和PspA类型的肺炎球菌菌株攻击免疫小鼠后其存活情况证明了基因免疫引发交叉保护的能力。此外,免疫小鼠免受肺炎球菌静脉内和气管内攻击。与用PspA免疫的结果相似,用pspA进行基因免疫的小鼠的存活是由抗体介导的。免疫7个月后保护水平没有下降。这些结果支持使用基因免疫来引发针对细胞外病原体的保护性免疫反应。