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福氏志贺菌2a菌株CVD 1203的ΔaroAΔvirG缺失株作为黏膜志贺菌疫苗及用于递送产肠毒素大肠杆菌抗原的活载体疫苗的进一步特性研究。

Further characterization of delta aroA delta virG Shigella flexneri 2a strain CVD 1203 as a mucosal Shigella vaccine and as a live-vector vaccine for delivering antigens of enterotoxigenic Escherichia coli.

作者信息

Noriega F R, Losonsky G, Wang J Y, Formal S B, Levine M M

机构信息

Center for Vaccine Development, University of Maryland School of Medicine, Baltimore 21201, USA.

出版信息

Infect Immun. 1996 Jan;64(1):23-7. doi: 10.1128/iai.64.1.23-27.1996.

Abstract

The use of attenuated delta aroA delta virG Shigella flexneri 2a strain CVD 1203 as a live vector for enterotoxigenic Escherichia coli (ETEC) antigens is reported. CVD 1203 alone or expressing colonization factor antigen fimbriae and CS3 fibrillae of ETEC was given to guinea pigs and mice, orogastrically (o.g.) or intranasally (i.n.). CVD 1203 given i.n. elicited high titers of antilipopolysaccharide (anti-LPS) immunoglobulin A (IgA) and was protective in guinea pigs against a homologous conjunctival challenge. Whereas a strong IgA response against colonization factor antigen CS3, and Shigella LPS was detected in tears and serum of guinea pigs after o.g. or i.n. immunization, the i.n. route elicited significantly higher antibody titers. A strong serum IgG response was also observed against the ETEC antigens, although no serum anti-LPS IgG response was detected. The immune response in mice followed a pattern similar to that in guinea pigs, and the difference between the responses after o.g. and i.n. administration was even more remarkable.

摘要

据报道,减毒的aroA缺失、virG缺失的福氏志贺菌2a菌株CVD 1203被用作产肠毒素大肠杆菌(ETEC)抗原的活载体。单独的CVD 1203或表达ETEC的定居因子抗原菌毛和CS3菌毛的CVD 1203通过口服或鼻内途径给予豚鼠和小鼠。鼻内给予的CVD 1203可诱导高滴度的抗脂多糖(抗LPS)免疫球蛋白A(IgA),并对豚鼠抵抗同源结膜攻击具有保护作用。虽然在口服或鼻内免疫后,在豚鼠的眼泪和血清中检测到针对定居因子抗原CS3和志贺菌LPS的强烈IgA反应,但鼻内途径诱导的抗体滴度明显更高。还观察到针对ETEC抗原的强烈血清IgG反应,尽管未检测到血清抗LPS IgG反应。小鼠的免疫反应模式与豚鼠相似,口服和鼻内给药后反应的差异甚至更显著。

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