藏猪白细胞介素-15基因的克隆及其聚乙二醇和PEI修饰壳聚糖纳米粒重组质粒对小鼠口蹄疫免疫的佐剂作用

Xiaoping Wan , Xiao Yang , Suqiong Zhan , Jianlin Chen , Wenkui Sun , Yihui Chen , Kai Zeng , Jiangling Li , Yiren Gu , Zezhou Wang , Rui Liu , Xuebin Lu , Rong Gao
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The total RNA of HEK293 cell was isolated in 48<!--> <!-->h, and the successful expression of IL-15 was detected by RT-PCR and the supernatant of HEK293 cells was found to stimulate significant proliferation of lymphoblasts of pig. Subsequently, VRTIL-15 packed with CS-PEG-PEI was utilized to intramuscularly inoculate Kunming female mice at the age of 21 days. Their bloods were collected before and after inoculation on 1, 2, 3, 4 and 5 weeks to detect the changes of innate and adaptive immunity of animals. The results were found that Th and Tc, specific antibody to FMD, IgG, IgG1, IgG2a content markedly increased in the blood of treated mice compared with the control group (P<!--> <!-->&lt;<!--> <!-->0.05). The mRNA expression of TLR1, TLR4 TLR6, TLR9, TGF-β, IL-2, IL-4, IL-6 and IL-23 were significantly higher in the treated group than those of the control (P<!--> <!-->&lt;<!--> <!-->0.05). 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引用次数: 0

摘要

首先从藏猪活化淋巴细胞中克隆IL-15 cDNA,然后将其亚克隆到VR1020中构建重组VRTIL-15质粒,研究其在动物体内外的生物学效应。用PEG-PEI修饰的壳聚糖(CS-PEG-PEI)包埋VRTIL-15,转染HEK293细胞,初步研究VRTIL-15在真核细胞中的表达。48 h分离HEK293细胞总RNA, RT-PCR检测IL-15的成功表达,发现HEK293细胞上清能显著刺激猪淋巴细胞增殖。随后,用VRTIL-15包装CS-PEG-PEI,于21日龄昆明雌性小鼠肌内接种。分别于接种前、接种后1、2、3、4、5周采血,检测动物先天免疫和适应性免疫的变化。结果发现,与对照组相比,治疗组小鼠血液中Th、Tc、口蹄疫特异性抗体、IgG、IgG1、IgG2a含量显著升高(P <0.05)。治疗组TLR1、TLR4、TLR6、TLR9、TGF-β、IL-2、IL-4、IL-6、IL-23 mRNA表达量均显著高于对照组(P <0.05)。上述结果表明,CS-PEG-PEI包裹VRTIL-15可显著提高动物的先天免疫、体液免疫和细胞适应性免疫,可启发开发有效的免疫佐剂,提高动物对口蹄疫的综合免疫保护。
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Cloning of interleukin-15 gene of Tibetan pig and adjuvant effect of its recombinant plasmids packed with PEG and PEI modified chitosan nanoparticles on immunity of mice to FMD vaccination

IL-15 cDNA of Tibetan pig was firstly cloned from its activated lymphocytes, and then was sub-cloned into VR1020 to construct recombinant VRTIL-15 plasmid to study the in vitro and in vivo biological effects on animal. The VRTIL-15 was entrapped with chitosan modified with PEG-PEI (CS-PEG-PEI) to transfect HEK293 cells for the preliminary study of its expression in eukaryotic cells. The total RNA of HEK293 cell was isolated in 48 h, and the successful expression of IL-15 was detected by RT-PCR and the supernatant of HEK293 cells was found to stimulate significant proliferation of lymphoblasts of pig. Subsequently, VRTIL-15 packed with CS-PEG-PEI was utilized to intramuscularly inoculate Kunming female mice at the age of 21 days. Their bloods were collected before and after inoculation on 1, 2, 3, 4 and 5 weeks to detect the changes of innate and adaptive immunity of animals. The results were found that Th and Tc, specific antibody to FMD, IgG, IgG1, IgG2a content markedly increased in the blood of treated mice compared with the control group (P < 0.05). The mRNA expression of TLR1, TLR4 TLR6, TLR9, TGF-β, IL-2, IL-4, IL-6 and IL-23 were significantly higher in the treated group than those of the control (P < 0.05). These results indicate that the VRTIL-15 wrapped with CS-PEG-PEI can significantly improve the innate, humoral and cellular adaptive immunity of animal, which could inspire the development of effective immune adjuvant to improve the comprehensive immune protection of animals against FMD.

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