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构建一种抗志贺毒素2抗体以控制肠出血性大肠杆菌O157:H7的严重感染。

Engineering an anti-Stx2 antibody to control severe infections of EHEC O157:H7.

作者信息

Ma Ying, Mao Xuhu, Li Jun, Li Haixia, Feng Youjun, Chen Hongzhang, Luo Ping, Gu Jiang, Yu Shu, Zeng Hao, Guo Gang, Yang Kang, Zou Quanming

机构信息

Department of Clinical Microbiology & Clinical Immunology, College of Medical Laboratory, Third Military Medical University, Chongqing 400038, PR China.

出版信息

Immunol Lett. 2008 Dec 22;121(2):110-5. doi: 10.1016/j.imlet.2008.09.008. Epub 2008 Nov 11.

Abstract

Enterohaemorrhagic Escherichia coli (EHEC) O157:H7, a primary enteric pathogen, has been implicated in a wide spectrum of food/water-borne infectious diseases such as hemorrhagic colitis (HC) and hemolyticuremic syndrome (HUS). Effective treatments for EHEC O157:H7 induced disease are not available yet. Shiga-toxin 2 (Stx2) has been related to clinical manifestations of HUS, suggesting its critical role in pathology following infection with EHEC O157:H7. Here we report the development of four anti-Stx2-Monoclonal antibodies (McAbs) (5F3and 5C11 for Stx2A, and 1A4 and 1A5 for Stx2B), all of which have strong immunogenicity and neutralization activities in vitro and in vivo. The full-length cDNA coding for anti-Stx2A McAb, 5F3, was cloned and an engineered antibody was developed whose therapeutic effects were evaluated. Our data indicate that the engineered scFv together with two new McAbs may be applicable for the prevention and therapy of EHEC induced pathology.

摘要

肠出血性大肠杆菌(EHEC)O157:H7是一种主要的肠道病原体,与多种食源性/水源性传染病有关,如出血性结肠炎(HC)和溶血尿毒综合征(HUS)。目前尚无针对EHEC O157:H7所致疾病的有效治疗方法。志贺毒素2(Stx2)与HUS的临床表现有关,表明其在EHEC O157:H7感染后的病理过程中起关键作用。在此,我们报告了四种抗Stx2单克隆抗体(McAbs)(针对Stx2A的5F3和5C11,以及针对Stx2B的1A4和1A5)的研制情况,所有这些抗体在体外和体内均具有很强的免疫原性和中和活性。编码抗Stx2A McAb 5F3的全长cDNA被克隆,并开发了一种工程抗体,对其治疗效果进行了评估。我们的数据表明,工程化单链抗体片段(scFv)与两种新的McAbs可能适用于预防和治疗EHEC引起的病理状况。

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