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迈向鉴定保护性B细胞表位:肺炎链球菌表面蛋白A的故事

Towards Identifying Protective B-Cell Epitopes: The PspA Story.

作者信息

Khan Naeem, Jan Arif T

机构信息

Glycobiology Group, Max Planck Institute of Colloids and Interfaces (MPG)Potsdam, Germany.

Department of Medical Biotechnology, Yeungnam UniversityGyeongsan, South Korea.

出版信息

Front Microbiol. 2017 May 2;8:742. doi: 10.3389/fmicb.2017.00742. eCollection 2017.

Abstract

Pneumococcal surface protein A (PspA) is one of the most abundant cell surface protein of (). PspA variants are structurally and serologically diverse and help evade complement-mediated phagocytosis of , which is essential for its survival in the host. PspA is currently been screened for employment in the generation of more effective (serotype independent) vaccine to overcome the limitations of polysaccharide based vaccines, providing serotype specific immune responses. The cross-protection eliciting regions of PspA localize to the α-helical and proline rich regions. Recent data indicate significant variation in the ability of antibodies induced against the recombinant PspA variants to recognize distinct strains. Hence, screening for the identification of the topographical repertoire of B-cell epitopes that elicit cross-protective immune response seems essential in the engineering of a superior PspA-based vaccine. Herein, we revisit epitope identification in PspA and the utility of hybridoma technology in directing the identification of protective epitope regions of PspA that can be used in vaccine research.

摘要

肺炎球菌表面蛋白A(PspA)是()中最丰富的细胞表面蛋白之一。PspA变体在结构和血清学上具有多样性,有助于逃避补体介导的()吞噬作用,这对其在宿主体内的存活至关重要。目前正在筛选PspA,以便用于生产更有效的(血清型非依赖性)疫苗,以克服基于多糖的疫苗的局限性,后者提供血清型特异性免疫反应。PspA的交叉保护诱导区域定位于α螺旋和富含脯氨酸的区域。最近的数据表明,针对重组PspA变体诱导产生的抗体识别不同()菌株的能力存在显著差异。因此,筛选鉴定能引发交叉保护免疫反应的B细胞表位的拓扑结构库,对于构建更优质的基于PspA的疫苗似乎至关重要。在此,我们重新审视PspA中的表位鉴定以及杂交瘤技术在指导鉴定可用于疫苗研究的PspA保护性表位区域方面的效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3813/5411445/0887d176fb20/fmicb-08-00742-g001.jpg

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