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5型和8型金黄色葡萄球菌荚膜多糖-蛋白质结合疫苗

Staphylococcus aureus types 5 and 8 capsular polysaccharide-protein conjugate vaccines.

作者信息

Robbins John B, Schneerson Rachel, Horwith Gary, Naso Robert, Fattom Ali

机构信息

National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Am Heart J. 2004 Apr;147(4):593-8. doi: 10.1016/j.ahj.2004.01.012.

Abstract

BACKGROUND

Staphylococcus aureus, the first or second most common pathogen isolated from patients, is capsulated; there are at least 12 capsular types, and types 5 and 8 comprise approximately 85% of blood. Types 5 and 8, composed of a trisaccharide repeat unit including a mannose uronic acid and 2 fucoses, are non-immunogenic. As protein conjugates, they induce opsonophagocytic antibodies that confer type-specific active and passive protection in mice.

METHODS

A phase II study of patients with end-stage renal disease showed that these conjugates induced approximately one third of the immunoglobulin G antibody of healthy individuals. Increasing the dose to 100 microg of polysaccharide induced levels similar to that in healthy individuals injected with 25 microg.

RESULTS

In a double-blinded randomized and controlled study of patients undergoing renal dialysis, the conjugates induced statistically significant protection against bacteremia for as long as 10 months after immunization. The estimated protective level was 80 microg Ab/mL. At re-injection approximately 2 years later, 83 of 83 recipients responded with protective levels.

CONCLUSIONS

Conjugate vaccine-induced antibodies to the types 5 and 8 capsular polysaccharide antibodies of S aureus prevent bacteremia caused by this pathogen. The extent and duration of conjugate-induced immunity can be extended by re-immunization approximately 1 year later. Studies of patients undergoing cardiovascular surgery who would be immunized with the staphylococcus conjugates when they are immunologically intact are planned.

摘要

背景

金黄色葡萄球菌是从患者体内分离出的最常见的一种或第二种病原体,它具有荚膜;至少有12种荚膜类型,其中5型和8型约占血液感染的85%。5型和8型由包含甘露糖醛酸和2个岩藻糖的三糖重复单元组成,无免疫原性。作为蛋白质偶联物,它们可诱导调理吞噬抗体,在小鼠体内赋予型特异性主动和被动保护。

方法

一项针对终末期肾病患者的II期研究表明,这些偶联物诱导产生的免疫球蛋白G抗体约为健康个体的三分之一。将多糖剂量增加到100微克可诱导出与注射25微克的健康个体相似的抗体水平。

结果

在一项针对接受肾透析患者的双盲随机对照研究中,偶联物在免疫后长达10个月的时间里对菌血症诱导出具有统计学意义的保护作用。估计的保护水平为80微克抗体/毫升。在大约2年后再次注射时,83名接受者中有83名产生了具有保护水平的反应。

结论

金黄色葡萄球菌5型和8型荚膜多糖抗体的偶联疫苗可预防该病原体引起的菌血症。偶联物诱导的免疫程度和持续时间可通过大约1年后的再次免疫来延长。计划对在免疫功能正常时接受葡萄球菌偶联疫苗免疫的心血管手术患者进行研究。

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