人乳头瘤病毒感染肽基疫苗设计的新进展

Maryam Moazami-goodarzi, R. Fotouhi-Ardakani, Ali Afgar
{"title":"人乳头瘤病毒感染肽基疫苗设计的新进展","authors":"Maryam Moazami-goodarzi, R. Fotouhi-Ardakani, Ali Afgar","doi":"10.1504/IJBRA.2017.10006936","DOIUrl":null,"url":null,"abstract":"To strength the potency of vaccines against infectious diseases, vaccines should be able to activate multiple arms of the immune system including innate and adaptive immunity. Moreover, genetic variation often occurs in infectious microorganisms can reduce the effectiveness of vaccines. Current vaccines and methods to immunisation against human papilloma virus, as a leading cause of different cancers, stimulate immune system moderately. In this study, to obtain highly effective responses, conserved Th and B-cell epitopes of L1 and CTL and Th epitopes of E7 are fused to helicobacter pylori NapA which is responsible for activation of innate immunity and direction favourable response to appropriate state. Finding the best conserved epitopes in order to induce better immune system may increase promising approach to achieve high-level immunity against infectious agents such as human papilloma virus (HPV). Thus, elevated immunity can be able to eradicate HPV vigorously. Designed construct can be useful as a peptide-based subunit vaccine to confer both preventive and therapeutic effects against all HPV16 subtypes.","PeriodicalId":434900,"journal":{"name":"Int. J. Bioinform. Res. Appl.","volume":"68 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2017-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Insilco new aspects of peptide-based vaccine designing for human papilloma virus infection\",\"authors\":\"Maryam Moazami-goodarzi, R. Fotouhi-Ardakani, Ali Afgar\",\"doi\":\"10.1504/IJBRA.2017.10006936\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"To strength the potency of vaccines against infectious diseases, vaccines should be able to activate multiple arms of the immune system including innate and adaptive immunity. Moreover, genetic variation often occurs in infectious microorganisms can reduce the effectiveness of vaccines. Current vaccines and methods to immunisation against human papilloma virus, as a leading cause of different cancers, stimulate immune system moderately. In this study, to obtain highly effective responses, conserved Th and B-cell epitopes of L1 and CTL and Th epitopes of E7 are fused to helicobacter pylori NapA which is responsible for activation of innate immunity and direction favourable response to appropriate state. Finding the best conserved epitopes in order to induce better immune system may increase promising approach to achieve high-level immunity against infectious agents such as human papilloma virus (HPV). Thus, elevated immunity can be able to eradicate HPV vigorously. Designed construct can be useful as a peptide-based subunit vaccine to confer both preventive and therapeutic effects against all HPV16 subtypes.\",\"PeriodicalId\":434900,\"journal\":{\"name\":\"Int. J. Bioinform. Res. Appl.\",\"volume\":\"68 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-08-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Int. J. Bioinform. Res. Appl.\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1504/IJBRA.2017.10006936\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Int. J. Bioinform. Res. Appl.","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1504/IJBRA.2017.10006936","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

为了增强疫苗对抗传染病的效力,疫苗应该能够激活免疫系统的多个分支,包括先天免疫和适应性免疫。此外,传染性微生物中经常发生的遗传变异会降低疫苗的有效性。人类乳头状瘤病毒是各种癌症的主要病因,目前的疫苗和免疫方法对免疫系统的刺激是适度的。本研究将保守的L1和CTL的Th和b细胞表位以及E7的Th表位融合到幽门螺杆菌NapA中,以获得高效的应答,而幽门螺杆菌NapA负责激活先天免疫并将有利应答引导到适当状态。寻找最佳保守的抗原表位,以诱导更好的免疫系统,可能增加有希望的方法来实现高水平的免疫,以对抗传染性病原体,如人乳头瘤病毒(HPV)。因此,提高免疫力可以有力地根除HPV。设计的构建体可作为一种基于肽的亚单位疫苗,对所有HPV16亚型具有预防和治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Insilco new aspects of peptide-based vaccine designing for human papilloma virus infection
To strength the potency of vaccines against infectious diseases, vaccines should be able to activate multiple arms of the immune system including innate and adaptive immunity. Moreover, genetic variation often occurs in infectious microorganisms can reduce the effectiveness of vaccines. Current vaccines and methods to immunisation against human papilloma virus, as a leading cause of different cancers, stimulate immune system moderately. In this study, to obtain highly effective responses, conserved Th and B-cell epitopes of L1 and CTL and Th epitopes of E7 are fused to helicobacter pylori NapA which is responsible for activation of innate immunity and direction favourable response to appropriate state. Finding the best conserved epitopes in order to induce better immune system may increase promising approach to achieve high-level immunity against infectious agents such as human papilloma virus (HPV). Thus, elevated immunity can be able to eradicate HPV vigorously. Designed construct can be useful as a peptide-based subunit vaccine to confer both preventive and therapeutic effects against all HPV16 subtypes.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信