• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

疟疾亚单位疫苗的应用前景。

The case for a subunit vaccine against malaria.

机构信息

Department of Biochemistry, La Trobe University, Victoria, Australia.

出版信息

Trends Parasitol. 2011 Aug;27(8):330-4. doi: 10.1016/j.pt.2011.04.003. Epub 2011 May 17.

DOI:10.1016/j.pt.2011.04.003
PMID:21592861
Abstract

New technologies and some disillusionment with subunit vaccines has led to increased interest in the development of whole parasite vaccines for malaria. Instead, the current priority should be to build on the partial success of the recombinant protein sporozoite vaccine, RTS,S. There are many possible options for delivering a subunit vaccine but the simplest option, formulating recombinant proteins in an adjuvant, should be fully explored. Numerous options exist for inducing heightened immune responses and for tackling the problem of diversity, but development of recombinant protein subunit vaccines requires a more detailed knowledge of the conformation of the leading vaccine candidates.

摘要

新技术和对亚单位疫苗的一些幻想破灭,导致人们对疟疾全寄生虫疫苗的开发产生了浓厚的兴趣。相反,目前的重点应该是在重组蛋白子孢子疫苗 RTS,S 的部分成功的基础上继续努力。有许多可能的选择可以用于输送亚单位疫苗,但最简单的选择,即将重组蛋白在佐剂中进行配方,应该得到充分的探索。有许多选择可以用来诱导更高的免疫反应和解决多样性的问题,但重组蛋白亚单位疫苗的开发需要更详细地了解主要候选疫苗的构象。

相似文献

1
The case for a subunit vaccine against malaria.疟疾亚单位疫苗的应用前景。
Trends Parasitol. 2011 Aug;27(8):330-4. doi: 10.1016/j.pt.2011.04.003. Epub 2011 May 17.
2
Pre-erythrocytic malaria vaccines to prevent Plasmodium falciparum malaria.用于预防恶性疟原虫疟疾的红细胞前期疟疾疫苗。
Chem Immunol. 2002;80:253-61.
3
Immune responses in mice induced by prime-boost schemes of the Plasmodium falciparum apical membrane antigen 1 (PfAMA1)-based DNA, protein and recombinant modified vaccinia Ankara vaccines.基于恶性疟原虫顶端膜抗原1(PfAMA1)的DNA、蛋白质和重组改良安卡拉痘苗疫苗的初免-加强免疫方案在小鼠中诱导的免疫反应。
Vaccine. 2006 Sep 11;24(37-39):6187-98. doi: 10.1016/j.vaccine.2006.05.099. Epub 2006 Jun 12.
4
Emerging rules for subunit-based, multiantigenic, multistage chemically synthesized vaccines.基于亚基的多抗原、多阶段化学合成疫苗的新规则
Acc Chem Res. 2008 Mar;41(3):377-86. doi: 10.1021/ar700120t. Epub 2008 Feb 12.
5
Malaria vaccine development using synthetic peptides as a technical platform.基于合成肽技术平台的疟疾疫苗研发。
Adv Immunol. 2012;114:107-49. doi: 10.1016/B978-0-12-396548-6.00005-6.
6
Immunogenicity of a recombinant malaria vaccine candidate, domain I+II of AMA-1 ectodomain, from Indian P. falciparum alleles.一种重组疟疾候选疫苗(恶性疟原虫AMA-1胞外结构域的I+II结构域,来自印度恶性疟原虫等位基因)的免疫原性。
Vaccine. 2008 Aug 18;26(35):4526-35. doi: 10.1016/j.vaccine.2008.06.031. Epub 2008 Jun 30.
7
A preliminary evaluation of a recombinant circumsporozoite protein vaccine against Plasmodium falciparum malaria. RTS,S Malaria Vaccine Evaluation Group.一种抗恶性疟原虫疟疾的重组环子孢子蛋白疫苗的初步评估。RTS,S疟疾疫苗评估小组。
N Engl J Med. 1997 Jan 9;336(2):86-91. doi: 10.1056/NEJM199701093360202.
8
The Plasmodium sporozoite survives RTS,S vaccination.疟原虫子孢子能在RTS,S疫苗接种后存活。
Trends Parasitol. 2005 Oct;21(10):456-61. doi: 10.1016/j.pt.2005.08.002.
9
Genetically attenuated malaria parasites as vaccines.基因减毒疟原虫作为疫苗
Expert Rev Vaccines. 2017 Aug;16(8):765-767. doi: 10.1080/14760584.2017.1341835. Epub 2017 Jun 16.
10
Evaluation of two long synthetic merozoite surface protein 2 peptides as malaria vaccine candidates.评估两种长合成裂殖子表面蛋白2肽作为疟疾疫苗候选物的情况。
Vaccine. 2009 May 5;27(20):2653-61. doi: 10.1016/j.vaccine.2009.02.081. Epub 2009 Mar 6.

引用本文的文献

1
The Application of Mesenchymal Stem Cells in Future Vaccine Synthesis.间充质干细胞在未来疫苗合成中的应用。
Vaccines (Basel). 2023 Oct 24;11(11):1631. doi: 10.3390/vaccines11111631.
2
Malaria vaccines: the 60-year journey of hope and final success-lessons learned and future prospects.疟疾疫苗:60年的希望之旅与最终成功——经验教训与未来展望
Trop Med Health. 2023 May 17;51(1):29. doi: 10.1186/s41182-023-00516-w.
3
Investigation of liposomal self-adjuvanting peptide epitopes derived from conserved blood-stage Plasmodium antigens.
来源于血期疟原虫保守抗原的脂质体自佐剂肽表位的研究。
PLoS One. 2022 Mar 11;17(3):e0264961. doi: 10.1371/journal.pone.0264961. eCollection 2022.
4
Disordered epitopes as peptide vaccines.作为肽疫苗的无序表位
Pept Sci (Hoboken). 2018 May;110(3):e24067. doi: 10.1002/pep2.24067. Epub 2018 Apr 14.
5
The case for a rational genome-based vaccine against malaria.基于合理基因组的疟疾疫苗的情况。
Front Microbiol. 2015 Jan 22;5:741. doi: 10.3389/fmicb.2014.00741. eCollection 2014.
6
Plasmodium berghei circumsporozoite protein encapsulated in oligomannose-coated liposomes confers protection against sporozoite infection in mice.包裹在低聚甘露糖包被脂质体中的伯氏疟原虫环子孢子蛋白可使小鼠免受子孢子感染。
Malar J. 2014 Nov 5;13:426. doi: 10.1186/1475-2875-13-426.
7
Protective immunity against Trichinella spiralis infection induced by a multi-epitope vaccine in a murine model.多表位疫苗在小鼠模型中诱导的抗旋毛虫感染保护性免疫
PLoS One. 2013 Oct 10;8(10):e77238. doi: 10.1371/journal.pone.0077238. eCollection 2013.
8
The evolutionary consequences of blood-stage vaccination on the rodent malaria Plasmodium chabaudi.血阶段疫苗接种对啮齿动物疟原虫 Plasmodium chabaudi 的进化后果。
PLoS Biol. 2012;10(7):e1001368. doi: 10.1371/journal.pbio.1001368. Epub 2012 Jul 31.