Fattom A, Schneerson R, Szu S C, Vann W F, Shiloach J, Karakawa W W, Robbins J B
National Institute of Child Health and Human Development, Bethesda, Maryland 20892.
Infect Immun. 1990 Jul;58(7):2367-74. doi: 10.1128/iai.58.7.2367-2374.1990.
Epidemiological, serological and in vitro phagocytosis experiments provide evidence that the newly discovered type 5 and type 8 capsular polysaccharides (CPs) are both virulence factors and protective antigens for bacteremia caused by Staphylococcus aureus. Neither type 5 nor type 8 CP elicited serum antibodies when injected into mice. These two CPs were bound to Pseudomonas aeruginosa exotoxin A (ETA) to form conjugates by using the synthetic scheme devised for the CP (Vi) of Salmonella typhi and of pneumococcus type 12F (A. Fattom, W. F. Vann, S. C. Szu, A. Sutton, X. Li, D. Bryla, G. Schiffman, J. B. Robbins, and R. Schneerson, Infect. Immun. 56:2292-2298, 1988; S. C. Szu, A. L. Stone, J. D. Robbins, R. Schneerson, and J. B. Robbins, J. Exp. Med. 166:1510-1524, 1987). Both S. aureus CP-ETA conjugates elicited a rise in CP antibodies. As components of conjugates, both S. aureus CPs acquired T-cell-dependent properties, as shown by their ability to respond to carrier priming and to stimulate booster responses. The conjugate-induced antibodies facilitated type-specific opsonization of S. aureus by human polymorphonuclear leukocytes. The conjugates also induced ETA antibodies which neutralized the native toxin in vitro. Clinical studies of these two conjugates for active or passive immunization of patients at risk for S. aureus bacteremia are planned.
流行病学、血清学及体外吞噬实验表明,新发现的5型和8型荚膜多糖(CPs)既是金黄色葡萄球菌引起菌血症的毒力因子,也是保护性抗原。将5型和8型CPs注射到小鼠体内均未引发血清抗体。利用为伤寒沙门菌的CP(Vi)和12F型肺炎球菌设计的合成方案(A. Fattom、W. F. Vann、S. C. Szu、A. Sutton、X. Li、D. Bryla、G. Schiffman、J. B. Robbins和R. Schneerson,《感染与免疫》56:2292 - 2298,1988;S. C. Szu、A. L. Stone、J. D. Robbins、R. Schneerson和J. B. Robbins,《实验医学杂志》166:1510 - 1524,1987),将这两种CPs与铜绿假单胞菌外毒素A(ETA)结合形成偶联物。两种金黄色葡萄球菌CP - ETA偶联物均引发了CP抗体的升高。作为偶联物的组分,两种金黄色葡萄球菌CPs均获得了T细胞依赖性特性,这表现为它们对载体引发产生反应并刺激加强反应的能力。偶联物诱导产生的抗体促进了人多形核白细胞对金黄色葡萄球菌的型特异性调理作用。偶联物还诱导产生了能在体外中和天然毒素的ETA抗体。计划对这两种偶联物进行临床研究,用于对有金黄色葡萄球菌菌血症风险的患者进行主动或被动免疫。