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口服 coated PEDV-loaded 微球在断奶仔猪中引发了 PEDV 特异性免疫。

Oral administration of coated PEDV-loaded microspheres elicited PEDV-specific immunity in weaned piglets.

机构信息

State Key Laboratory of Biocontrol, School of Life Science, Sun Yat-sen University, Guangzhou 510006, China.

Wen's Group Academy, Wen's Foodstuffs Group Co, Ltd, Xinxing, Guangdong 527400, China.

出版信息

Vaccine. 2018 Oct 29;36(45):6803-6809. doi: 10.1016/j.vaccine.2018.09.014. Epub 2018 Sep 20.

Abstract

Porcine epidemic diarrhea virus (PEDV) infects pigs of all ages by invading villous epithelial cells of the small intestine causing severe diarrhea with high mortality rate in suckling piglets. Mucosal immunity is believed to play an important role in PEDV control and mucosal delivery of vaccines induces mucosal immunity more efficiently than parenteral vaccination. In this study, coated PEDV-loaded microspheres with the size range of 700-900 μm in diameter were developed by centrifugal granulation-fluidized bed coating and demonstrated as an effective oral delivery system to protect PEDV antigens against the complex gastrointestinal environment by detecting the live virus particles in microspheres after the simulated gastric fluid treatment and the PEDV RNA in fecal swabs collected from all weaned piglets (100%) orally inoculated with coated PEDV-loaded microspheres. Weaned piglets orally immunized with coated PEDV-loaded microspheres developed higher levels of PEDV-specific antibodies (IgG and IgA) in their sera and saliva than those negative control groups (p < 0.001 or p < 0.01). Furthermore, neutralization assays demonstrated that serum antibodies in coated PEDV-loaded microspheres groups could significantly inhibit virus infection in Vero cells, compared to PEDV only group (p < 0.05). Overall, our results indicate that the coated PEDV-loaded microspheres might serve as an effective way to induce PEDV-specific mucosal immunity in pigs against PEDV.

摘要

猪流行性腹泻病毒(PEDV)通过感染小肠的绒毛状上皮细胞感染所有年龄段的猪,导致仔猪死亡率很高的严重腹泻。黏膜免疫被认为在 PEDV 控制中发挥重要作用,黏膜疫苗接种比全身疫苗接种更有效地诱导黏膜免疫。在这项研究中,通过离心造粒-流化床包衣法制备了直径在 700-900μm 范围内的包被 PEDV 载药微球,并证明其是一种有效的口服递送系统,可通过检测模拟胃液处理后微球中的活病毒颗粒和来自所有断奶仔猪粪便拭子中的 PEDV RNA 来保护 PEDV 抗原免受复杂的胃肠道环境影响。用包被的 PEDV 载药微球口服免疫的断奶仔猪在血清和唾液中产生了更高水平的 PEDV 特异性抗体(IgG 和 IgA),比阴性对照组高(p<0.001 或 p<0.01)。此外,中和试验表明,与 PEDV 组相比,包被的 PEDV 载药微球组的血清抗体能够显著抑制 Vero 细胞中的病毒感染(p<0.05)。总体而言,我们的结果表明,包被的 PEDV 载药微球可能是诱导猪针对 PEDV 产生 PEDV 特异性黏膜免疫的有效方法。

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