Mucosal delivery of a transmission-blocking DNA vaccine encoding Giardia lamblia CWP2 by Salmonella typhimurium bactofection vehicle

被引:34
作者
Abdul-Wahid, Aws [1 ]
Faubert, Gaetan [1 ]
机构
[1] McGill Univ, Inst Parasitol, Quebec City, PQ H9X 3V9, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
giardia; encystation; CWP2; transmission-blocking DNA vaccine; bactofection; Salmonella typhimurium STM1 strain;
D O I
10.1016/j.vaccine.2007.10.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this study, we investigated the use of Salmonella typhimurium (STM1 strain) as a bactofection vehicle to deliver a transmission-blocking DNA vaccine (TBDV) plasmid to the intestinal immune system. The gene encoding the full length cyst wall protein-2 (CWP2) from Giardia lamblia was subcloned into the pCDNA3 mammalian expression vector and stably introduced into S. typhimurium STM1. Eight-week-old female BALB/c mice were orally immunized every 2 weeks, for a total of three immunizations. Vaccinated and control mice were sacrificed I week following the last injection. Administration of the DNA vaccine led to the production of CVVP2-specific cellular immune responses characterized by a mixed Th1/Th2 response. Using ELISA, antigen-specific IgA and IgG antibodies were detected in intestinal secretions. Moreover, analysis of sera demonstrated that the DNA immunization also stimulated the production of CWP2-specific IgG antibodies that were mainly of the IgG2a isotype. Finally, challenge infection with live Giardia muris cysts revealed that mice receiving the CWP2-encoding DNA vaccine were able to reduce cyst shedding by similar to 60% compared to control mice. These results demonstrate, for the first time, the development of parasite transmission-blocking immunity at the intestinal level following the administration of a mucosal DNA vaccine delivered by S. typhimurium STM1. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:8372 / 8383
页数:12
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