Wittner M K, Fox E N
Infect Immun. 1977 Jan;15(1):104-8. doi: 10.1128/iai.15.1.104-108.1977.
Purified streptococcal M proteins precipitated with alum (APM) were used to immunize mice. A trivalent vaccine of serotypes 1, 3, and 12 protected mice against challenges by homologous live streptococci and also conferred protection against serotypes 6 and 14 but not against a strain of group B streptococci. Monovalent APM vaccines afforded homologous protection and restricted heterologous protection. The extent of heterologous protection was a function of serotype combinations and was also dose dependent. Rabbit antisera exhibiting strong opsonic activities were active in vitro and in passive mouse protection only for homologous serotypes. Mouse antisera did not passively transfer protection and were not bactericidal in vitro. It was concluded that homologous and heterologous active mouse protection was most likely a result of shared antigenic determinants of the various M proteins although protection of mice could not be measured as a function of circulating anti-M antibodies.
用明矾沉淀的纯化链球菌M蛋白(APM)免疫小鼠。1、3和12型三价疫苗可保护小鼠免受同源活链球菌的攻击,也可提供针对6型和14型的保护,但不能保护小鼠免受B组链球菌菌株的攻击。单价APM疫苗提供同源保护并限制异源保护。异源保护的程度是血清型组合的函数,并且也是剂量依赖性的。表现出强调理活性的兔抗血清仅在体外以及对同源血清型的被动小鼠保护中具有活性。小鼠抗血清不能被动转移保护作用,并且在体外没有杀菌作用。得出的结论是,同源和异源活性小鼠保护最可能是各种M蛋白共享抗原决定簇的结果,尽管小鼠的保护不能作为循环抗M抗体的函数来测量。