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新型酵母疫苗通过微线蛋白 16 诱导针对弓形虫的保护性免疫应答。

Protective immune response against Toxoplasma gondii elicited by a novel yeast-based vaccine with microneme protein 16.

机构信息

Shandong Institute of Parasitic Diseases, Shandong Academy of Medical Sciences, 11 Taibai Middle Road, Jining City, Shandong Province 272033, China.

Shandong Institute of Parasitic Diseases, Shandong Academy of Medical Sciences, 11 Taibai Middle Road, Jining City, Shandong Province 272033, China.

出版信息

Vaccine. 2018 Jun 22;36(27):3943-3948. doi: 10.1016/j.vaccine.2018.05.072. Epub 2018 May 21.

DOI:10.1016/j.vaccine.2018.05.072
PMID:29793893
Abstract

Toxoplasma gondii is an obligate intracellular protozoan that can invade all eukaryotic cells and infect all warm-blood animals, causing the important zoonosis toxoplasmosis. Invasion of host cells is the key step necessary for T. gondii to complete its life cycle and microneme proteins play an important role in attachment and invasion of host cells. Microneme protein 16 (TgMIC16) is a new protective protein in T. gondii and belongs to transmembrane microneme proteins (TM-MIC). The TM-MICs are released onto the parasite's surface as complexes capable of interacting with host cell receptors. In the present study, we expressed the TgMIC16 protein on the surface of Saccharomyce cerevisiae (pCTCON2-TgMIC16/EBY100) and evaluated it as a potential vaccine for BALB/c mice against challenge infection with the RH strain of T. gondii. We immunized BALB/c mice both orally and intraperitoneally. After three immunizations, the immune response was evaluated by measuring antibody levels, lymphocyte proliferative responses, percentages of CD4 and CD8 T lymphocytes, cytokine production, and the survival times of challenged mice. The results showed that the pCTCON2-TgMIC16/EBY100 vaccine stimulated humoral and cellular immune responses. In addition, mice immunized with the pCTCON2-TgMIC16/EBY100 vaccine showed increased survival times compared with non-immunized controls. In summary, TgMIC16 displayed on the cell surface of S. cerevisiae could be used as potential vaccine against toxoplasmosis.

摘要

刚地弓形虫是一种专性细胞内原生动物,能够侵入所有真核细胞并感染所有温血动物,导致重要的人畜共患病弓形虫病。宿主细胞的入侵是刚地弓形虫完成其生命周期的关键步骤,微线蛋白在宿主细胞的附着和入侵中起着重要作用。微线蛋白 16(TgMIC16)是刚地弓形虫中的一种新的保护性蛋白,属于跨膜微线蛋白(TM-MIC)。TM-MIC 作为能够与宿主细胞受体相互作用的复合物,释放到寄生虫表面。在本研究中,我们在酿酒酵母(pCTCON2-TgMIC16/EBY100)表面表达了 TgMIC16 蛋白,并评估其作为针对 RH 株刚地弓形虫感染的 BALB/c 小鼠的潜在疫苗。我们对 BALB/c 小鼠进行口服和腹腔内免疫。经过三次免疫后,通过测量抗体水平、淋巴细胞增殖反应、CD4 和 CD8 T 淋巴细胞的百分比、细胞因子产生以及受挑战小鼠的存活时间来评估免疫反应。结果表明,pCTCON2-TgMIC16/EBY100 疫苗刺激了体液和细胞免疫反应。此外,与未免疫对照组相比,用 pCTCON2-TgMIC16/EBY100 疫苗免疫的小鼠存活时间延长。综上所述,展示在酿酒酵母细胞表面的 TgMIC16 可用作抗弓形虫病的潜在疫苗。

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