|本期目录/Table of Contents|

[1]刘昕彤,黄焕会,舒建洪,等.猪流行性腹泻病毒的多表位 mRNA疫苗设计与免疫评价[J].浙江理工大学学报,2026,55-56(自科二):198-206.
 LIU Xintong,HUANG Huanhui,SHU Jianhong,et al.Design and immunological evaluation of a multi-epitope mRNA vaccine againstporcine epidemic diarrhea viru[J].Journal of Zhejiang Sci-Tech University,2026,55-56(自科二):198-206.
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猪流行性腹泻病毒的多表位 mRNA疫苗设计与免疫评价()

浙江理工大学学报[ISSN:1673-3851/CN:33-1338/TS]

卷:
55-56
期数:
2026年自科第二期
页码:
198-206
栏目:
出版日期:
2026-03-15

文章信息/Info

Title:
Design and immunological evaluation of a multi-epitope mRNA vaccine againstporcine epidemic diarrhea viru
文章编号:
1673-3851(2026) 03-0198-09
作者:
刘昕彤 黄焕会 舒建洪 金伟波
1. 浙江理工大学生命科学与医药学院 ,杭州 310018;2. 浙江理工大学绍兴生物医药研究院 ,浙江绍兴 312366
Author(s):
LIU Xintong HUANG Huanhui SHU JianhongJIN Weibo
1. College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou 310018, China; 2. Shaoxing Academy of Biomedicine, Zhejiang Sci-Tech University, Shaoxing312366, China
关键词:
猪流行性腹泻病毒多表位mRNA疫苗免疫信息学抗原表位免疫原性
分类号:
S858.28
文献标志码:
A
摘要:
为解决猪流行性腹泻病毒(Porcine epidemic diarrhea virus,PEDV) 现有疫苗保护力不足的问题 , 结合 免疫信息学与 mRNA技术 ,设计并构建一种基于多表位抗原(multi-epitopeantigen,ME) 的新型疫苗 。利用 VaxiJen 和 ANTIGENpro抗原性预测工具 , 以从 PEDV结构蛋白中筛选的 S蛋白(Q91AV1) 和 N蛋白(Q07499) 为候选抗 原 ,分别采用 IEDB、ABCpred和 NetMHCpan软件预测了 25条 B细胞优势表位和3条 T细胞优势表位 ,并通过柔性 连接肽将其串联整合 , 引入 Foldon三聚体结构及分泌信号肽构建 ME序列; 采用 mRNA-LNP递送系统制备 ME mRNA疫苗 ,并通过小鼠免疫实验评估该疫苗的免疫原性 。结果显示 :ME/S1mRNA联合免疫组在小鼠首次免疫 后 ,其 PEDV特异性免疫球蛋白 G(Immunoglobulin G, IgG) 抗体水平 OD450 nm 值为 1.250±0.068, 显著高于 S1 mRNA单免疫组 OD450 nm 值(0.816±0.074) 和传统灭活疫苗组 OD450 nm 值(0.805±0.065);ME/S1mRNA联合免 疫组在小鼠加强免疫后 ,联合组抗体滴度进一步提升 ,其 OD450 nm 值为 1.681±0.100,仍显著高于单免疫组 OD450 nm 值(1.238±0.074) 与传统灭活疫苗组 OD450 nm 值(1.164±0.114);ME与 S1mRNA联合免疫的多表位设计可通过 协同激发 B/T细胞应答 ,增强PEDV免疫效果 。该文结果为 PEDV防控提供了高效候选策略 ,并为其他冠状病毒 类动物疫苗的设计与开发提供了技术参考。

参考文献/References:

[1]Zhang H,Zou C C,Ouyang P,et al.Global dynamics of porcine enteric coronavirus PEDV epidemiology,evolution,and transmission[J].Molecular Biology and Evolution,2023,40 (3): msad052.

[2]张洋,欧云文,马春霞,等.猪流行性腹泻疫苗研究进展[J]. 中国 畜牧兽医,2024,51(11):5004-5013.

[3]Kong F,Jia H,Xiao Q,et al.Prevention and control of swine enteric coronaviruses in China:A review of vaccine development and application[J].Vaccines,2024,12(1):11.

[4]Li Z,Ma Z,Li Y,et al.Porcine epidemic diarrhea virus: Molecular mechanisms of attenuation and vaccines[J].Microbial Pathogenesis,2020,149:104553.

[5]Kirchdoerfer RN,Bhandari M,Martini O,et al.Structure and immune recognition of the porcine epidemic diarrhea virus spike protein[J].Structure,2021,29(4):385-392.

[6]Lin F,Zhang H,LiL,et al.PEDV:Insights and advances into types,function,structure,and receptor recognition [J]. Viruses,2022,14(8):1744.

[7]Zhao Y,Fan B,Song X,et al.PEDV-spike-protein-expressing mRNA vaccine protects piglets against PEDV challenge[J]. mBio,2024,15(2):e0295823.

[8]Song X,Li Y,Wang C,et al.Efficacy evaluation of a bivalent subunit vaccine against epidemic PEDV heterologous strains with low cross-protection[J].Journal of Virology,2024,98 (10):e0130924.

[9]Yang D,Su M,Li C,et al.Isolation and characterization of a variant subgroup GII-a porcine epidemic diarrhea vir us strain in China [J].Microbial Pathogenesis,2020,140:103922.

[10]Wei Y,Qiu T,Ai Y,et al.Advances of computational methods enhance the development of multi-epitope vaccines [J].Briefings in Bioinformatics,2024,26(1):bbaf055.

[11]De Groot AS,Moise L,Terry F,et al.Better epitope discovery,precision immune engineering,and accelerated vaccine design using immunoinformatics tools[J].Frontiers in Immunology,2020,11:442.

[12]Qin Y,Tu K,Teng Q,et al.Identification of novel T-Cell epitopes on infectious bronchitis virus N protein and development of a multi-epitope vaccine [J]. Journal of Virology,2021,95(17):e0066721.

[13]Lamb Y N.BNT162b2 mRNA COVID-19 vaccine:First approval[J].Drugs,2021,81(4):495-501.

[14]Gote V,Bolla PK,Kommineni N,et al.A comprehensive review of mRNA vaccines [J].International Journal of Molecular Sciences,2023,24(3):2700.

[15]Jain R,Jain A,Verma SK.Prediction of epitope basedpeptides for vaccine development from complete proteome of novel corona virus ( SARS-COV-2) using immunoinformatics [ J ]. International Journal of Peptide Research and Therapeutics, 2021,27(3) :1729-1740.

[16] Wilkins M R, Gasteiger E, Bairoch A, et al. Protein identification and analysis tools in the ExPASy server[J]. Methodsin MolecularBiology,1999,112:531-552.

[17] DimitrovI, BangovI, Flower D R, et al. AllerTOP v. 2: A server for in silico prediction of allergens[J]. Journal of MolecularModeling , 2014, 20(6) :2278.

[18] YeM, LiS, LuoP, etal. GeneticvariationofE6, E7, andL1 genes of human papillomavirus 51 from Central China[J]. JournalofMedicalVirology , 2022, 94(6) :2811-2823.

[19] AimanS, Alhamhoom Y, AliF, etal. Multi-epitopechimeric vaccine design against emerging monkeypox virus via reverse vaccinologytechniques-abioinformaticsand immunoinformatics approac h[J] . Frontiersin Immunology, 2022, 13: 985450.

[20] 李世念 ,刘婉宁 ,陈亚萍 ,等. 基于免疫信息学方法设计针对猪 急性腹泻综合征冠状病毒 S、M及 E蛋白的多表位疫苗[J]. 中 国畜牧兽医 ,2022,49(3) :1057-1066.

[21] Doytchinova I A, Flower D R. VaxiJen: A server for prediction ofprotectiveantigens, tumourantigensand subunit vaccines[J]. BMCBioinformatics, 2007,8:4.

[22] Yan Z, Kim K, Kim H, etal. Next-generation IEDB tools: A platform forepitopeprediction and analysis[J]. Nucleic Acids Research, 2024, 52(W1) :W526-W532.

[23] LuoT, XinC, Liu H, etal. PotentialSLA Hp-4.0 haplotype- restrictedCTL epitopes identified from the membrane protein of PRRSV induce cell immune responses[J]. Frontiers in Microbiology, 2024, 15:1404558.

[24] Rasmussen M, Fenoy E, Harndahl M, et al. Pan-Specific predictionofPeptide-MHCclassIcomplexstability, acorrelate ofT cell immunogenicity[J]. The Journal of Immunology, 2016, 197(4) :1517-1524.

[25] ZhangY, ZhaiS, HuangH, etal. Efficientsignalsequenceof mRNA vaccinesenhancestheantigen expression to expand the immune protection against viral infection [J]. Journal of Nanobiotechnology, 2024, 22(1) :295.

[26] PapanikolopoulouK, TeixeiraS, BelrhaliH, etal. Adenovirus fibreshaftsequences foldinto the native triple beta-spiralfold when N-terminallyfusedtothebacteriophageT4fibritinfoldon trimerisation motif[J]. Journal of Molecular Biology, 2004, 342(1) :219-227.

相似文献/References:

[1]张秋桠,刘高鹏,刘芹,等.猪流行性腹泻病毒RT-PCR检测方法的建立[J].浙江理工大学学报,2022,47-48(自科四):629.
 ZHANG Qiuya,LIU Gaopeng,LIU Qin,et al.Establishment of a RTPCR detection method for porcine epidemic diarrhea virus[J].Journal of Zhejiang Sci-Tech University,2022,47-48(自科二):629.

备注/Memo

备注/Memo:
收稿日期 : 2025-04-07 网络出版日期 : 2025-11-03基金项目 : 国家自然科学基金项目(32172496)作者简介 : 刘昕彤(1999— ) ,女 ,辽宁朝阳人 ,硕士研究生 ,主要从事 AI辅助药物发现方向的研究。通信作者 : 金伟波 ,E-mail:jwb@zstu. edu. cn
更新日期/Last Update: 2026-03-06