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金黄色葡萄球菌凝聚因子A和荚膜多糖在体内的异质性表达:对疫苗设计的启示

Heterogeneous in vivo expression of clumping factor A and capsular polysaccharide by Staphylococcus aureus: implications for vaccine design.

作者信息

Nanra Jasdeep S, Timofeyeva Yekaterina, Buitrago Sandra M, Sellman Bret R, Dilts Deborah A, Fink Pamela, Nunez Lorna, Hagen Michael, Matsuka Yury V, Mininni Terri, Zhu Duzhang, Pavliak Viliam, Green Bruce A, Jansen Kathrin U, Anderson Annaliesa S

机构信息

Wyeth Vaccine Research, 401 N. Middletown Road, Pearl River, NY 10965, USA.

出版信息

Vaccine. 2009 May 26;27(25-26):3276-80. doi: 10.1016/j.vaccine.2009.01.062. Epub 2009 Feb 5.

Abstract

There is a clear unmet medical need for a vaccine that would prevent infections from Staphylococcus aureus (S. aureus). To validate antigens as potential vaccine targets it has to be demonstrated that the antigens are expressed in vivo. Using murine bacteremia and wound infection models, we demonstrate that the expression of clumping factor A (ClfA) and capsular polysaccharide antigens are heterogeneous and dependent on the challenge strains examined and the in vivo microenvironment. We also demonstrate opsonophagocitic activity mediated by either antigen is not impeded by the presence of the other antigen. The data presented in this report support a multiantigen approach for the development of a prophylactic S. aureus vaccine to ensure broad coverage against this versatile pathogen.

摘要

对于一种能够预防金黄色葡萄球菌(S. aureus)感染的疫苗,存在明显未满足的医学需求。为了验证抗原作为潜在疫苗靶点,必须证明抗原在体内表达。利用小鼠菌血症和伤口感染模型,我们证明了凝聚因子A(ClfA)和荚膜多糖抗原的表达是异质性的,并且取决于所检测的攻击菌株和体内微环境。我们还证明,一种抗原介导的调理吞噬活性不会受到另一种抗原存在的阻碍。本报告中呈现的数据支持采用多抗原方法来开发预防性金黄色葡萄球菌疫苗,以确保对这种多面性病原体具有广泛的覆盖范围。

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