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一种基于OspA的DNA疫苗可保护小鼠免受伯氏疏螺旋体感染。

An OspA-based DNA vaccine protects mice against infection with Borrelia burgdorferi.

作者信息

Luke C J, Carner K, Liang X, Barbour A G

机构信息

Department of Microbiology, University of Texas Health Science Center at San Antonio, USA.

出版信息

J Infect Dis. 1997 Jan;175(1):91-7. doi: 10.1093/infdis/175.1.91.

Abstract

Immunization with recombinant OspA protein of Borrelia burgdorferi protects against experimental Lyme disease. In the present study, mice were injected intramuscularly with plasmid DNA (VR2210) encoding strain B31 OspA. In this vector, the ospA-coding sequence was under transcriptional control of the cytomegalovirus immediate early promoter. For negative and positive controls, mice were immunized with either the plasmid vector without an osp-coding sequence or recombinant OspA protein, respectively. Mice immunized with VR2210 DNA produced OspA-specific antibodies that bound to B. burgdorferi in a whole cell ELISA and inhibited the growth of a homologous strain of B. burgdorferi. Immunization with VR2210 protected mice against challenge with 2 infectious strains of B. burgdorferi, Sh-2-82 and N40. These results indicate that vaccination with plasmid DNA expressing OspA is an efficacious method for providing a protective response against B. burgdorferi infection.

摘要

用重组伯氏疏螺旋体OspA蛋白进行免疫可预防实验性莱姆病。在本研究中,给小鼠肌肉注射编码B31菌株OspA的质粒DNA(VR2210)。在该载体中,ospA编码序列受巨细胞病毒立即早期启动子的转录控制。作为阴性和阳性对照,分别用不含osp编码序列的质粒载体或重组OspA蛋白对小鼠进行免疫。用VR2210 DNA免疫的小鼠产生了OspA特异性抗体,这些抗体在全细胞ELISA中与伯氏疏螺旋体结合,并抑制同源伯氏疏螺旋体菌株的生长。用VR2210免疫可保护小鼠免受两种感染性伯氏疏螺旋体菌株Sh-2-82和N40的攻击。这些结果表明,用表达OspA的质粒DNA进行疫苗接种是提供针对伯氏疏螺旋体感染的保护性反应的有效方法。

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