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脑膜炎奈瑟菌的自转运蛋白A:一种通过表达克隆检测到的强效CD4 + T细胞和B细胞刺激抗原。

Auto-transporter A protein of Neisseria meningitidis: a potent CD4+ T-cell and B-cell stimulating antigen detected by expression cloning.

作者信息

Ait-Tahar K, Wooldridge K G, Turner D P, Atta M, Todd I, Ala'Aldeen D A

机构信息

Meningococcal Research Group, Divisions of Microbiology and Immunology, University of Nottingham, Nottingham NG7 2UH, UK.

出版信息

Mol Microbiol. 2000 Sep;37(5):1094-105. doi: 10.1046/j.1365-2958.2000.02061.x.

Abstract

A meningococcal genomic expression library was screened for potent CD4+ T-cell antigens, using patients' peripheral blood lymphocytes (PBLs). One of the most promising positive clones was fully characterized. The recombinant meningococcal DNA contained a single, incomplete, open reading frame (ORF), which was fully reconstructed with reference to available genomic sequence data. The gene was designated autA (auto-transporter A) as its peptide sequence shares molecular characteristics of the auto-transporter family of proteins. Only a single copy of this gene was detected in the meningococcal, and none in the gonococcal, genomic sequence databases. The complete autA gene, when cloned into an expression vector, expressed a protein of approximately 68 kDa. Purified rAutA recalled strong secondary T-cell responses in PBLs of patients and some healthy donors, and induced strong primary T-cell responses in healthy donors. The human B-cell immunogenicity and cross-reactivity of AutA, purified under native conditions, was confirmed in dot immunoblot experiments. Immunoblots with rabbit polyclonal antibodies to rAutA demonstrated the conserved nature, antigenicity and cross-reactivity of AutA amongst meningococci of different serogroups and strains representing different hypervirulent lineages. AutA showed homology with another meningococcal and gonococcal ORF (designated AutB). AutB was cloned and expressed and used to raise an autB-specific antiserum. Immunoblot experiments indicated that AutB is not expressed in meningococci and does not cross-react with AutA. Thus, AutA, being a potent CD4+ T-cell and B-cell-stimulating antigen, which is highly conserved, deserves further investigation as a potential vaccine candidate.

摘要

利用患者外周血淋巴细胞(PBL)对脑膜炎球菌基因组表达文库进行筛选,以寻找有效的CD4 + T细胞抗原。对其中一个最有前景的阳性克隆进行了全面表征。重组脑膜炎球菌DNA包含一个单一的、不完整的开放阅读框(ORF),根据现有的基因组序列数据对其进行了完全重建。该基因被命名为autA(自转运蛋白A),因为其肽序列具有自转运蛋白家族蛋白质的分子特征。在脑膜炎球菌基因组序列数据库中仅检测到该基因的一个拷贝,而在淋球菌基因组序列数据库中未检测到。当完整的autA基因克隆到表达载体中时,表达出一种约68 kDa的蛋白质。纯化的rAutA在患者和一些健康供体的PBL中引发了强烈的继发性T细胞反应,并在健康供体中诱导了强烈的原发性T细胞反应。在斑点免疫印迹实验中证实了天然条件下纯化的AutA的人B细胞免疫原性和交叉反应性。用针对rAutA的兔多克隆抗体进行的免疫印迹显示,AutA在代表不同高毒力谱系的不同血清群和菌株的脑膜炎球菌中具有保守性、抗原性和交叉反应性。AutA与另一个脑膜炎球菌和淋球菌的ORF(命名为AutB)具有同源性。克隆并表达了AutB,并用于制备抗AutB特异性抗血清。免疫印迹实验表明,AutB在脑膜炎球菌中不表达,且与AutA无交叉反应。因此,AutA作为一种高效的CD4 + T细胞和B细胞刺激抗原,具有高度保守性,作为潜在的疫苗候选物值得进一步研究。

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