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针对产肠毒素大肠杆菌(ETEC)CFA/I菌毛的DNA免疫

DNA immunisation against the CFA/I fimbriae of enterotoxigenic Escherichia coli (ETEC).

作者信息

Alves A M, Lásaro M O, Almeida D F, Ferreira L C

机构信息

Laboratório de Fisiologia Celular, Instituto de Biofísica Carlos Chagas Filho, UFRJ-CCS, Cidade Universitária, RJ 21941-590, Rio de Janeiro, Brazil.

出版信息

Vaccine. 2000 Nov 22;19(7-8):788-95. doi: 10.1016/s0264-410x(00)00244-9.

Abstract

The CFA/I fimbria promotes the attachment of enterotoxigenic Escherichia coli (ETEC) to the surface of human enterocytes. The generation of a protective immune response requires the induction of antibodies able to block the CFA/I-mediated binding of ETEC to receptors located on the small intestine epithelium or on the surface of human red blood cells, in hemagglutination tests. An eukaryotic expression plasmid, pBLCFA, encoding the CFA/I gene under the control of the human cytomegalovirus major immediate-early promoter was constructed as a prototype DNA vaccine against ETEC. pBLCFA-tranfected BHK-21 cells secreted a peptide cross-reacting with a monoclonal antibody raised against CFA/I subunits. BALB/c mice immunized intramuscularly with one or two doses of purified pBLCFA developed CFA/I-specific serum antibodies for at least 52 weeks, composed predominantly of the IgG1 subclass. pBLCFA-induced antibodies bind mainly to epitopes exposed on the surface of intact CFA/I fimbriae and do not react with immune recessive epitopes found in other ETEC fimbra sharing amino acid homologies with CFA/I. Furthermore, pBLCFA-induced antibodies were able to block the adhesive properties of the CFA/I fimbriae, as evaluated by the ability to inhibit the hemagglutination promoted by CFA/I-expressing ETEC cells. These results suggest that secretion of CFA/I encoded by pBLCFA preserves important conformational epitopes required for the generation of protective antibodies against the adhesive properties of the CFA/I fimbriae and open new perspectives for the development of DNA vaccines against enteric bacterial pathogens.

摘要

CFA/I菌毛促进产肠毒素大肠杆菌(ETEC)与人肠上皮细胞表面的附着。产生保护性免疫反应需要诱导出能够在血凝试验中阻断ETEC通过CFA/I介导与位于小肠上皮或人红细胞表面的受体结合的抗体。构建了一种真核表达质粒pBLCFA,其在人巨细胞病毒主要立即早期启动子的控制下编码CFA/I基因,作为针对ETEC的原型DNA疫苗。用pBLCFA转染的BHK - 21细胞分泌一种与针对CFA/I亚基产生的单克隆抗体发生交叉反应的肽。用一剂或两剂纯化的pBLCFA肌肉注射免疫的BALB/c小鼠产生CFA/I特异性血清抗体至少52周,主要由IgG1亚类组成。pBLCFA诱导的抗体主要结合完整CFA/I菌毛表面暴露的表位,不与在与CFA/I具有氨基酸同源性的其他ETEC菌毛中发现的免疫隐性表位反应。此外,通过抑制表达CFA/I的ETEC细胞促进的血凝的能力评估,pBLCFA诱导的抗体能够阻断CFA/I菌毛的黏附特性。这些结果表明,pBLCFA编码的CFA/I的分泌保留了产生针对CFA/I菌毛黏附特性的保护性抗体所需的重要构象表位,并为开发针对肠道细菌病原体的DNA疫苗开辟了新的前景。

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