首页> 外文期刊>Biomaterials >The influence of antibodies on Staphylococcus epidermidis adherence to polyvinylpyrrolidone-coated silicone elastomer in experimental biomaterial-associated infection in mice.
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The influence of antibodies on Staphylococcus epidermidis adherence to polyvinylpyrrolidone-coated silicone elastomer in experimental biomaterial-associated infection in mice.

机译:在小鼠实验性生物材料相关感染中,抗体对表皮葡萄球菌粘附于聚乙烯吡咯烷酮涂层的有机硅弹性体的影响。

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摘要

Biomaterial-associated infection (BAI) is a major problem in modern medicine, and is often caused by Staphylococcus epidermidis. We aimed to raise monoclonal antibodies (mAbs) against major surface protein antigens of S. epidermidis, and to assess their possible protective activity in experimental BAI. Mice were vaccinated with a cell wall protein preparation of S. epidermidis. A highly immunodominant antigen was identified as Accumulation-associated protein (Aap). mAbs against Aap and against surface-exposed lipoteichoic acid (LTA) were used for passive immunization of mice in experimental biomaterial-associated infection. Neither anti-Aap nor anti-LTA mAbs showed protection. Either with or without antibodies, tissue surrounding the implants was more often culture positive than the implants themselves, but bacterial adherence to the implants was significantly increased in mice injected with anti-LTA. In vitro, anti-Aap and anti-LTA did show binding to S. epidermidis, but no opsonic activity was observed. We conclude that antibodies against S. epidermidis LTA or Aap showed no opsonic activity and did not protect mice against BAI. Moreover, the increase in binding to implanted biomaterial suggests that passive immunization may increase the risk for BAI.
机译:生物材料相关感染(BAI)是现代医学中的一个主要问题,通常是由表皮葡萄球菌引起的。我们旨在提高针对表皮葡萄球菌主要表面蛋白抗原的单克隆抗体(mAb),并评估其在实验性BAI中的可能的保护活性。给小鼠接种表皮葡萄球菌的细胞壁蛋白制剂。高度免疫优势的抗原被确定为积累相关蛋白(Aap)。针对Aap和针对表面暴露的脂磷壁酸(LTA)的单克隆抗体用于实验性生物材料相关感染的小鼠被动免疫。抗Aap和抗LTA mAb均未显示保护作用。无论有无抗体,植入物周围的组织通常比植入物本身培养阳性,但是在注射了抗LTA的小鼠中细菌对植入物的粘附明显增加。在体外,抗Aap和抗LTA确实显示与表皮葡萄球菌结合,但未观察到调理活性。我们得出的结论是,针对表皮葡萄球菌LTA或Aap的抗体没有调理活性,也不能保护小鼠免受BAI侵害。此外,与植入的生物材料的结合增加表明被动免疫可能会增加BAI的风险。

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