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针对定居因子抗原I(CFA/I)菌毛亚基的单克隆抗体可抑制与人肠上皮细胞的结合,并对表达异源定居因子的产肠毒素大肠杆菌起到保护作用。

Monoclonal antibodies against fimbrial subunits of colonization factor antigen I (CFA/I) inhibit binding to human enterocytes and protect against enterotoxigenic Escherichia coli expressing heterologous colonization factors.

作者信息

Rudin A, Olbe L, Svennerholm A M

机构信息

Department of Medical Microbiology and Immunology, Göteborg University, Sweden.

出版信息

Microb Pathog. 1996 Jul;21(1):35-45. doi: 10.1006/mpat.1996.0040.

Abstract

Enterotoxigenic Escherichia coli (ETEC) bind to enterocytes in the small intestine by means of antigenically distinct colonization factors (CFs). By immunizing with isolated subunits of CFA/I fimbriae we have previously produced monoclonal antibodies (MAbs) that cross-react immunologically in vitro with several CFs. Two of these MAbs [S(subunit)-CFA/ I 17:8 and S-CFA/I 5:6] were found to significantly inhibit the binding of ETEC strains expressing either homologous or heterologous CFs, i.e. CFA/I and CS4, to isolated human jejunal enterocytes. The two MAbs also conferred passive protection against fluid accumulation in rabbit ileal loops caused by CFA/I-as well as CS4-expressing ETEC strains. Immunoelectron microscopy studies showed that both MAbs bound specifically to CFA/I as well as to CS4 fimbriae expressed on bacteria. These results indicate the possibility to induce anti-CF antibodies that can protect against ETEC infection caused by bacteria expressing not only homologous but also heterologous CFs, by immunizing with fimbrial subunits.

摘要

产肠毒素大肠杆菌(ETEC)借助抗原性不同的定居因子(CFs)与小肠中的肠上皮细胞结合。我们之前通过用CFA/I菌毛的分离亚基进行免疫,制备了在体外与多种CFs发生免疫交叉反应的单克隆抗体(MAbs)。发现其中两种MAbs [S(亚基)-CFA/I 17:8和S-CFA/I 5:6]能显著抑制表达同源或异源CFs(即CFA/I和CS4)的ETEC菌株与分离的人空肠肠上皮细胞的结合。这两种MAbs还对由表达CFA/I以及CS4的ETEC菌株引起的兔回肠袢液体蓄积提供了被动保护。免疫电子显微镜研究表明,这两种MAbs均能特异性结合细菌表面表达的CFA/I以及CS4菌毛。这些结果表明,通过用菌毛亚基进行免疫,有可能诱导产生抗CF抗体,从而不仅能抵御表达同源CFs的细菌引起的ETEC感染,还能抵御表达异源CFs的细菌引起的ETEC感染。

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