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首页> 外文期刊>Infection and immunity >Recombinant ESAT-6-Like Proteins Provoke Protective Immune Responses against Invasive Staphylococcus aureus Disease in a Murine Model
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Recombinant ESAT-6-Like Proteins Provoke Protective Immune Responses against Invasive Staphylococcus aureus Disease in a Murine Model

机译:重组ESAT-6样蛋白在鼠模型中引发针对侵袭性金黄色葡萄球菌疾病的保护性免疫反应。

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Staphylococcus aureus is a common pathogen found in the community and in hospitals. Most notably, methicillin-resistant S. aureus is resistant to many antibiotics, which is a growing public health concern. The emergence of drug-resistant strains has prompted the search for alternative treatments, such as immunotherapeutic approaches. To date, most clinical trials of vaccines or of passive immunization against S. aureus have ended in failure. In this study, we investigated two ESAT-6-like proteins secreted by S. aureus, S. aureus EsxA (SaEsxA) and SaEsxB, as possible targets for a vaccine. Mice vaccinated with these purified proteins elicited high titers of anti-SaEsxA and anti-SaEsxB antibodies, but these antibodies could not prevent S. aureus infection. On the other hand, recombinant SaEsxA (rSaEsxA) and rSaEsxB could induce Th1- and Th17-biased immune responses in mice. Mice immunized with rSaEsxA and rSaEsxB had significantly improved survival rates when challenged with S. aureus compared with the controls. These findings indicate that SaEsxA and SaEsxB are two promising Th1 and Th17 candidate antigens which could be developed into multivalent and serotype-independent vaccines against S. aureus infection.
机译:金黄色葡萄球菌是在社区和医院中发现的常见病原体。最值得注意的是,耐甲氧西林的金黄色葡萄球菌对许多抗生素具有抗药性,这是公众对健康日益关注的问题。耐药菌株的出现促使人们寻求替代疗法,例如免疫治疗方法。迄今为止,大多数针对金黄色葡萄球菌的疫苗或被动免疫的临床试验都以失败告终。在这项研究中,我们调查了金黄色葡萄球菌分泌的两种ESAT-6样蛋白,金黄色葡萄球菌EsxA(SaEsxA)和SaEsxB,它们可能是疫苗的靶标。接种了这些纯化蛋白的小鼠引发了高滴度的抗SaEsxA和抗SaEsxB抗体,但这些抗体不能预防金黄色葡萄球菌感染。另一方面,重组SaEsxA(rSaEsxA)和rSaEsxB可以在小鼠体内诱导偏向Th1和Th17的免疫反应。与对照组相比,用金黄色葡萄球菌攻击的小鼠用rSaEsxA和rSaEsxB免疫后,其存活率显着提高。这些发现表明,SaEsxA和SaEsxB是两种有前途的Th1和Th17候选抗原,可以开发成多价且不依赖血清型的金黄色葡萄球菌感染疫苗。

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