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一种新型的抗原半胱氨酸蛋白酶 B 在感染旋毛虫的小鼠中诱导保护性免疫。

A novel antigenic cathepsin B protease induces protective immunity in Trichinella-infected mice.

机构信息

Sun Yat-sen University Zhongshan School of Medicine, Key Laboratory of Tropical Disease Control (Sun Yat-Sen University), Ministry of Education, Guangzhou 510080, China.

The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China.

出版信息

Vaccine. 2018 Jan 4;36(2):248-255. doi: 10.1016/j.vaccine.2017.11.048. Epub 2017 Dec 2.

Abstract

Trichinellosis is a foodborne disease that remains a public health hazard and an economic problem in food safety. Vaccines against the parasite can be an effective way to control this disease; however, commercial vaccines against Trichinella infection are not yet available. Trichinella cathepsin B proteins appear to be promising targets for vaccine development. Here, we reported for the first time the characterization of a novel cDNA that encodes Trichinella spiralis (T. spiralis) cathepsin B-like protease 2 gene (TsCPB2). The recombinant mature TsCPB2 protein was successfully expressed in E. coli system and purified with Ni-affinity chromatography. TsCPB2 expression was detected at all the developmental stages of T. spiralis and it was expressed as an excretory-secretory protein of T. spiralis muscle larvae. Immunization with TsCPB2 antigen induced a combination of humoral and cellular immune responses, which manifested as a mixed Th1/Th2 response, as well as remarkably elevated IgE level. Moreover, vaccination of mice with TsCPB2 that were subsequently challenged with T. spiralis larvae resulted in a 52.3% (P < .001) reduction in worm burden and a 51.2% (P < .001) reduction in muscle larval burden. Our results suggest that TsCPB2 induces protective immunity in Trichinella-infected mice and might be a novel vaccine candidate against trichinellosis.

摘要

旋毛虫病是一种食源性疾病,仍然是食品安全方面的公共卫生危害和经济问题。寄生虫疫苗可以是控制这种疾病的有效方法;然而,针对旋毛虫感染的商业疫苗尚未上市。旋毛虫组织蛋白酶 B 蛋白似乎是疫苗开发的有希望的靶标。在这里,我们首次报道了一种新的 cDNA 的特征,该 cDNA 编码旋毛虫(T. spiralis)组织蛋白酶 B 样蛋白酶 2 基因(TsCPB2)。重组成熟 TsCPB2 蛋白在大肠杆菌系统中成功表达,并通过 Ni 亲和层析纯化。TsCPB2 的表达在旋毛虫的所有发育阶段都被检测到,并且作为旋毛虫肌肉幼虫的分泌蛋白表达。用 TsCPB2 抗原免疫诱导了体液和细胞免疫反应的组合,表现为混合 Th1/Th2 反应,以及显著升高的 IgE 水平。此外,用 TsCPB2 对小鼠进行免疫接种,随后用旋毛虫幼虫进行攻虫,可使虫体负荷减少 52.3%(P <.001),肌肉幼虫负荷减少 51.2%(P <.001)。我们的结果表明,TsCPB2 诱导了感染旋毛虫的小鼠的保护性免疫,可能是一种针对旋毛虫病的新型疫苗候选物。

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