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用刚地弓形虫过氧化物还原酶1进行免疫可诱导小鼠对弓形虫病产生保护性免疫。

Immunization with Toxoplasma gondii peroxiredoxin 1 induces protective immunity against toxoplasmosis in mice.

作者信息

Fereig Ragab M, Kuroda Yasuhiro, Terkawi Mohamad Alaa, Mahmoud Motamed Elsayed, Nishikawa Yoshifumi

机构信息

National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Inada-cho, Obihiro, Hokkaido, Japan.

Department of Animal Medicine, Faculty of Veterinary Medicine, South Valley University, Qena City, Qena, Egypt.

出版信息

PLoS One. 2017 Apr 27;12(4):e0176324. doi: 10.1371/journal.pone.0176324. eCollection 2017.

Abstract

To develop a vaccine against Toxoplasma gondii, a vaccine antigen with immune-stimulating activity is required. In the present study, we investigated the immunogenicity and prophylactic potential of T. gondii peroxiredoxin 1 (TgPrx1). The TgPrx1 was detected in the ascitic fluid of mice 6 days postinfection, while specific antibody levels were low in the sera of chronically infected mice. Treatment of murine peritoneal macrophages with recombinant TgPrx1 triggered IL-12p40 and IL-6 production, but not IL-10 production. In response to TgPrx1, activation of NF-kB and IL-6 production were confirmed in mouse macrophage cell line (RAW 264.7). These results suggest the immune-stimulating potentials of TgPrx1. Immunization of mice with recombinant TgPrx1 stimulated specific antibody production (IgG1 and IgG2c). Moreover, spleen cell proliferation and interferon-gamma production significantly increased in the TgPrx1- sensitized cells from mice immunized with the same antigen. Immunization with TgPrx1 also increased mouse survival and decreased cerebral parasite burden against lethal T. gondii infection. Thus, our results suggest that TgPrx1 efficiently induces humoral and cellular immune responses and is useful as a new vaccine antigen against toxoplasmosis.

摘要

为研发一种抗弓形虫的疫苗,需要一种具有免疫刺激活性的疫苗抗原。在本研究中,我们调查了弓形虫过氧化物还原酶1(TgPrx1)的免疫原性和预防潜力。感染后6天在小鼠腹水中检测到TgPrx1,而慢性感染小鼠血清中的特异性抗体水平较低。用重组TgPrx1处理小鼠腹腔巨噬细胞可引发IL-12p40和IL-6的产生,但不会引发IL-10的产生。在小鼠巨噬细胞系(RAW 264.7)中,对TgPrx1的反应证实了NF-κB的激活和IL-6的产生。这些结果表明TgPrx1具有免疫刺激潜力。用重组TgPrx1免疫小鼠可刺激特异性抗体产生(IgG1和IgG2c)。此外,在用相同抗原免疫的小鼠的TgPrx1致敏细胞中,脾细胞增殖和干扰素-γ产生显著增加。用TgPrx1免疫还提高了小鼠的存活率,并降低了致死性弓形虫感染的脑内寄生虫负荷。因此,我们的结果表明TgPrx1能有效诱导体液免疫和细胞免疫反应,可作为一种抗弓形虫病的新型疫苗抗原。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f901/5407612/fa2b5b402772/pone.0176324.g001.jpg

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