Schaffer Adam C, Lee Jean C
Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, PBB-B-422, 75 Francis street, Boston, MA 02115, USA.
Infect Dis Clin North Am. 2009 Mar;23(1):153-71. doi: 10.1016/j.idc.2008.10.005.
Staphylococcus aureus is an important pathogen in the hospital and in the community, and it is increasingly resistant to multiple antibiotics. A nonantimicrobial approach to controlling S aureus is needed. The most extensively tested vaccine against S aureus, which is a capsular polysaccharide-based vaccine known as StaphVAX, showed promise in an initial phase 3 trial, but was found to be ineffective in a confirmatory trial, leading to its development being halted. Likewise, a human IgG preparation known as INH-A21 (Veronate) with elevated levels of antibodies to the staphylococcal surface adhesins ClfA and SdrG made it into phase 3 testing, where it failed to show a clinical benefit. Several novel antigens are being tested for potential inclusion in a staphylococcal vaccine, including cell wall-anchored adhesin proteins and exotoxins. Given the multiple and sometimes redundant virulence factors of S aureus that enable it to be such a crafty pathogen, if a vaccine is to prove effective, it will have to be multicomponent, incorporating several surface proteins, toxoids, and surface polysaccharides.
金黄色葡萄球菌是医院和社区中的一种重要病原体,并且它对多种抗生素的耐药性日益增强。因此需要一种非抗菌方法来控制金黄色葡萄球菌。针对金黄色葡萄球菌测试最为广泛的疫苗是一种基于荚膜多糖的疫苗,称为葡萄球菌疫苗(StaphVAX),它在最初的3期试验中显示出前景,但在一项验证性试验中被发现无效,导致其研发停止。同样,一种名为INH-A21(Veronate)的人IgG制剂,其针对葡萄球菌表面粘附素ClfA和SdrG的抗体水平升高,进入了3期试验,但未显示出临床益处。目前正在测试几种新型抗原,以确定它们是否有可能被纳入葡萄球菌疫苗,包括细胞壁锚定粘附素蛋白和外毒素。鉴于金黄色葡萄球菌具有多种有时是冗余的毒力因子,使其成为一种狡猾的病原体,如果一种疫苗要证明有效,它必须是多组分的,包含几种表面蛋白、类毒素和表面多糖。