Matthews-Greer J M, Gilleland H E
J Infect Dis. 1987 Jun;155(6):1282-91. doi: 10.1093/infdis/155.6.1282.
Outer membrane (OM) protein F (porin) was purified by extraction from polyacrylamide gels of cell envelope proteins of the Pseudomonas aeruginosa PA01 strain. Mice were immunized intramuscularly with 10 micrograms of protein F preparation on days 1 and 14 and then subjected to burn and challenge on day 28. Protein F immunization afforded significant protection above that provided by PA01 lipopolysaccharide (LPS) immunization against subsequent challenge with six of six heterologous LPS immunotype strains of P. aeruginosa. By an ELISA, the murine immune response revealed an IgG titer of 5,120 to protein F by day 30. Immunoblot analysis of antisera from protein F-immunized mice revealed bands with both protein F and protein H of cell envelopes of all immunotypes tested. Active immunization with OM protein H did not, however, afford significant protection to mice in this burned mouse model. These data show the efficacy of OM protein F as a protective vaccine in a murine model representative of human infection.
外膜(OM)蛋白F(孔蛋白)是通过从铜绿假单胞菌PA01菌株的细胞包膜蛋白聚丙烯酰胺凝胶中提取而纯化得到的。在第1天和第14天,给小鼠肌肉注射10微克蛋白F制剂,然后在第28天进行烧伤并给予攻击。与PA01脂多糖(LPS)免疫相比,蛋白F免疫为小鼠提供了显著的保护作用,使其免受随后六种异源LPS免疫型铜绿假单胞菌菌株攻击的影响。通过酶联免疫吸附测定(ELISA),到第30天时,小鼠免疫反应显示针对蛋白F的IgG滴度为5120。对蛋白F免疫小鼠的抗血清进行免疫印迹分析,结果显示在所有测试免疫型的细胞包膜中,蛋白F和蛋白H均出现条带。然而,在这个烧伤小鼠模型中,用OM蛋白H进行主动免疫并不能为小鼠提供显著的保护。这些数据表明,在代表人类感染的小鼠模型中,OM蛋白F作为一种保护性疫苗具有有效性。