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通过分泌与分子佐剂C3d-P28融合的30聚体寄生虫表位的减毒活沙门氏菌疫苗在小鼠中引发的针对旋毛虫肠内阶段的保护性免疫。

Protective immunity against enteral stages of Trichinella spiralis elicited in mice by live attenuated Salmonella vaccine that secretes a 30-mer parasite epitope fused to the molecular adjuvant C3d-P28.

作者信息

Pompa-Mera Ericka N, Arroyo-Matus Pablo, Ocaña-Mondragón Alicia, González-Bonilla César R, Yépez-Mulia Lilián

机构信息

Unidad de Investigación en Enfermedades Infecciosas y Parasitarias, Hospital de Pediatría, Centro Médico Nacional Siglo XXI, IMSS, Mexico City, Mexico; Unidad de Investigación Médica en Inmunología e Infectología, Hospital de Infectología, Centro Médico Nacional La Raza, IMSS, Mexico City, Mexico; Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City, Mexico.

Unidad de Investigación en Enfermedades Infecciosas y Parasitarias, Hospital de Pediatría, Centro Médico Nacional Siglo XXI, IMSS, Mexico City, Mexico.

出版信息

Res Vet Sci. 2014 Dec;97(3):533-45. doi: 10.1016/j.rvsc.2014.09.010. Epub 2014 Sep 28.

DOI:10.1016/j.rvsc.2014.09.010
PMID:25311159
Abstract

The development of a veterinary vaccine against T. spiralis infection is an alternative strategy to control trichinellosis. In an effort to develop an efficient vaccine, BALB/c mice were immunized with attenuated Salmonella enterica serovar Typhimurium SL3261 that expresses a 30-mer peptide (Ag30) derived from the gp43 of T. spiralis muscle larvae fused to three copies of the molecular adjuvant P28 (Ag30-P283) and it was either displayed on the surface or secreted by recombinant Salmonella strains. Salmonella strain secreting Ag30-P283, reduced the adult worm burden 92.8% following challenge with T. spiralis muscle larvae compared to 42% achieved by recombinant Salmonella displaying Ag30-P283 on the surface. The protection induced by secreted Ag30-P283 was associated with a mixed Th1/Th2 with predominance of Th2 phenotype, which was characterized by the production of IgG1, intestinal IgA antibodies and IL-5 secretion. This finding could provide an efficient platform technology for the design of novel vaccination strategies.

摘要

开发针对旋毛虫感染的兽用疫苗是控制旋毛虫病的一种替代策略。为了开发一种高效疫苗,用表达源自旋毛虫肌幼虫gp43的30肽(Ag30)并与三个分子佐剂P28拷贝融合(Ag30-P283)的减毒肠炎沙门氏菌血清型鼠伤寒沙门氏菌SL3261免疫BALB/c小鼠,该抗原要么展示在表面,要么由重组沙门氏菌菌株分泌。与表面展示Ag30-P283的重组沙门氏菌相比,分泌Ag30-P283的沙门氏菌菌株在用旋毛虫肌幼虫攻击后,成虫负荷降低了92.8%,而表面展示Ag30-P283的重组沙门氏菌降低了42%。分泌的Ag30-P283诱导的保护作用与以Th2表型为主的Th1/Th2混合反应有关,其特征是产生IgG1、肠道IgA抗体和分泌IL-5。这一发现可为新型疫苗接种策略的设计提供一个高效的平台技术。

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