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一种针对 感染的多表位疫苗 GILE 在小鼠中的应用。

A multi-epitope vaccine GILE against infection in mice.

机构信息

Qinghai University Medical College, Xining, Qinghai, China.

Research Center for High Altitude Medicine, Qinghai-Utah Joint Research Key Lab for High Altitude Medicine, Qinghai Provincial Key Laboratory of Plateau Medical Application, Key Laboratory of Ministry of Education, Qinghai University, Xining, Qinghai, China.

出版信息

Front Immunol. 2023 Jan 17;13:1091004. doi: 10.3389/fimmu.2022.1091004. eCollection 2022.

Abstract

INTRODUCTION

The objective of this study is to construct a multi-epitope vaccine GILE containing B-cell and T-cell epitopes against () infection based on the dominant epitopes of EMY162, LAP, and GLUT1.

METHODS

The structure and hydrophobicity of GILE were predicted by SWISSMODEL, pyMOL, SOPMA and VMD, and its sequence was optimized by Optimum™ Codon. The GILE gene was inserted into pCzn1 and transformed into Arctic express competent cells. IPTG was added to induce the expression of recombinant proteins. High-purity GILE recombinant protein was obtained by Ni-NTA Resin. BALB/c mice were immunized with GILE mixed with Freund's adjuvant, and the antibody levels and dynamic changes in the serum were detected by ELISA. Lymphocyte proliferation was detected by MTS. The levels of IFN-g and IL-4 were detected by ELISpot and flow cytometry (FCM). T cells were detected by FCM. The growth of hepatic cysts was evaluated by Ultrasound and their weights were measured to evaluate the immune protective effect of GILE.

RESULTS

The SWISS-MODEL analysis showed that the optimal model was EMY162 -LAP-LAP-LAP-LAP-EMY162. The SOPMA results showed that there were Alpha helix (14.88%), Extended strand (26.25%), Beta turn (3.73%) and Random coil (45.82%) in the secondary structure of GILE. The restriction enzyme digestion and sequencing results suggested that the plasmid pCzn1-GILE was successfully constructed. The SDSPAGE results indicated that the recombinant protein was 44.68 KD. The ELISA results indicated that mice immunized with GILE showed higher levels of serum antibodies compared to the PBS group. The FCM and ELISpot results indicated that mice immunized with GILE secreted more IFN-g and IL-4. Immunization with GILE also led to a significant decrease in the maximum diameter and weight of cysts and stimulated the production of CD4 and CD8 T Cell.

DISCUSSION

A multi-epitope vaccine GILE with good immunogenicity and antigenicity has been successfully constructed in this study, which may provide important theoretical and experimental bases for the prevention and treatment of infection.

摘要

简介

本研究旨在构建一种基于 EMY162、LAP 和 GLUT1 优势表位的多表位疫苗 GILE,以对抗 ()感染。

方法

使用 SWISSMODEL、pyMOL、SOPMA 和 VMD 预测 GILE 的结构和疏水性,并用 Optimum™ Codon 对其序列进行优化。将 GILE 基因插入 pCzn1 并转化为 Arctic express 感受态细胞。加入 IPTG 诱导重组蛋白表达。用 Ni-NTA Resin 获得高纯度 GILE 重组蛋白。用 GILE 混合弗氏佐剂免疫 BALB/c 小鼠,ELISA 检测血清抗体水平和动态变化。MTS 检测淋巴细胞增殖。ELISpot 和流式细胞术(FCM)检测 IFN-g 和 IL-4 水平。FCM 检测 T 细胞。超声评估肝囊肿生长,测量其重量评估 GILE 的免疫保护作用。

结果

SWISS-MODEL 分析表明,最优模型为 EMY162-LAP-LAP-LAP-LAP-EMY162。SOPMA 结果表明,GILE 的二级结构中存在α螺旋(14.88%)、延伸链(26.25%)、β转角(3.73%)和无规则卷曲(45.82%)。酶切和测序结果表明成功构建了质粒 pCzn1-GILE。SDSPAGE 结果表明重组蛋白大小为 44.68KD。ELISA 结果表明,GILE 免疫组小鼠血清抗体水平高于 PBS 组。FCM 和 ELISpot 结果表明,GILE 免疫组小鼠分泌更多 IFN-g 和 IL-4。GILE 免疫还导致囊肿最大直径和重量显著降低,并刺激 CD4 和 CD8 T 细胞产生。

讨论

本研究成功构建了一种具有良好免疫原性和抗原性的多表位疫苗 GILE,为 感染的防治提供了重要的理论和实验依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/758c/9887108/aca3843f2956/fimmu-13-1091004-g001.jpg

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