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疟疾疫苗的研发

Vaccine development against malaria.

作者信息

Matuschewski Kai

机构信息

Department of Parasitology, Heidelberg University School of Medicine, Germany.

出版信息

Curr Opin Immunol. 2006 Aug;18(4):449-57. doi: 10.1016/j.coi.2006.05.004. Epub 2006 Jun 12.

DOI:10.1016/j.coi.2006.05.004
PMID:16765576
Abstract

Malaria vaccine development aims to significantly reduce mortality and morbidity in the two high-risk groups: young children and pregnant women in sub-Saharan Africa. A pre-erythrocytic subunit vaccine, RTS,S, was recently evaluated in a first Phase IIb clinical trial in young children that live in a mesoendemic area of malaria transmission. The identification of a major parasite-encoded ligand that was found to be involved in pregnancy-associated malaria allows for the rational development of a tailor-made subunit vaccine for young women. The generation of transgenic yellow fever viruses and defined attenuated vaccine lines by reverse genetics are complementary approaches that might further boost the development of safe vaccines that elicit protective immune responses in this population.

摘要

疟疾疫苗的研发旨在大幅降低两个高危群体的死亡率和发病率,这两个群体分别是撒哈拉以南非洲地区的幼儿和孕妇。一种前红细胞亚单位疫苗RTS,S,最近在疟疾传播为中度流行地区居住的幼儿中进行了首次IIb期临床试验评估。一种主要的寄生虫编码配体被发现与妊娠相关疟疾有关,这使得为年轻女性量身定制亚单位疫苗的合理研发成为可能。通过反向遗传学产生转基因黄热病病毒和确定减毒疫苗株是互补的方法,可能会进一步推动在这一人群中引发保护性免疫反应的安全疫苗的研发。

相似文献

1
Vaccine development against malaria.疟疾疫苗的研发
Curr Opin Immunol. 2006 Aug;18(4):449-57. doi: 10.1016/j.coi.2006.05.004. Epub 2006 Jun 12.
2
Preerythrocytic malaria vaccine development.疟原虫前体细胞疫苗的研发。
Curr Opin Infect Dis. 2007 Oct;20(5):461-6. doi: 10.1097/QCO.0b013e3282ef6172.
3
Methods for determining vaccine efficacy and effectiveness and the main barriers to developing a fully deployable malaria vaccine.确定疫苗效力和效果的方法以及开发完全可部署的疟疾疫苗的主要障碍。
Am J Trop Med Hyg. 2007 Dec;77(6 Suppl):276-81.
4
Genetically modified Plasmodium highlights the potential of whole parasite vaccine strategies.转基因疟原虫凸显了全寄生虫疫苗策略的潜力。
Trends Immunol. 2005 Jun;26(6):295-7. doi: 10.1016/j.it.2005.04.005.
5
A case for whole-parasite malaria vaccines.全寄生虫疟疾疫苗的实例。
Int J Parasitol. 2007 Jun;37(7):705-12. doi: 10.1016/j.ijpara.2007.02.007. Epub 2007 Feb 28.
6
Pre-erythrocytic malaria vaccines: towards greater efficacy.红细胞前期疟疾疫苗:追求更高疗效。
Nat Rev Immunol. 2006 Jan;6(1):21-32. doi: 10.1038/nri1746.
7
The development of the RTS,S malaria vaccine candidate: challenges and lessons.疟疾候选疫苗RTS,S的研发:挑战与经验教训
Parasite Immunol. 2009 Sep;31(9):492-500. doi: 10.1111/j.1365-3024.2009.01143.x.
8
Genetically modified Plasmodium parasites as a protective experimental malaria vaccine.转基因疟原虫作为一种保护性实验性疟疾疫苗。
Nature. 2005 Jan 13;433(7022):164-7. doi: 10.1038/nature03188. Epub 2004 Dec 5.
9
Vaccines against malaria - an update.疟疾疫苗——最新进展
FEBS J. 2007 Sep;274(18):4680-7. doi: 10.1111/j.1742-4658.2007.05998.x.
10
Immune evasion by malaria parasites: a challenge for vaccine development.疟原虫的免疫逃避:疫苗研发面临的挑战
Curr Opin Immunol. 2009 Jun;21(3):321-30. doi: 10.1016/j.coi.2009.05.015. Epub 2009 Jun 1.

引用本文的文献

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A Fast-Track Phenotypic Characterization of Plasmodium falciparum Vaccine Antigens through Lyse-Reseal Erythrocytes Mediated Delivery (LyRED) of RNA Interference for Targeted Translational Repression.通过 Lyse-Reseal 红细胞介导的 RNA 干扰(LyRED)进行快速表型特征分析 ,实现靶向翻译抑制的恶性疟原虫疫苗抗原。
Methods Mol Biol. 2022;2410:539-553. doi: 10.1007/978-1-0716-1884-4_27.
2
Insights from modelling malaria vaccines for policy decisions: the focus on RTS,S.从疟疾疫苗模型中获得的政策决策见解:关注 RTS,S。
Malar J. 2021 Nov 18;20(1):439. doi: 10.1186/s12936-021-03973-y.
3
Disruption of plasmepsin-4 and merozoites surface protein-7 genes in Plasmodium berghei induces combined virulence-attenuated phenotype.
破坏伯氏疟原虫的裂殖体蛋白 4 和裂殖子表面蛋白 7 基因可导致毒力减弱的表型。
Sci Rep. 2011;1:39. doi: 10.1038/srep00039. Epub 2011 Jul 18.
4
Development of the malaria parasite in the skin of the mammalian host.疟原虫在哺乳动物宿主体内的皮肤中的发育。
Proc Natl Acad Sci U S A. 2010 Oct 26;107(43):18640-5. doi: 10.1073/pnas.1009346107. Epub 2010 Oct 4.
5
The Plasmodium serine-type SERA proteases display distinct expression patterns and non-essential in vivo roles during life cycle progression of the malaria parasite.疟原虫生活史进程中,丝氨酸型 SERA 蛋白酶表现出不同的表达模式和非必需的体内作用。
Cell Microbiol. 2010 Jun;12(6):725-39. doi: 10.1111/j.1462-5822.2009.01419.x. Epub 2009 Dec 21.
6
Vaccine potentials of an intrinsically unstructured fragment derived from the blood stage-associated Plasmodium falciparum protein PFF0165c.源自恶性疟原虫血液阶段相关蛋白PFF0165c的一个内在无序片段的疫苗潜力
Infect Immun. 2009 Dec;77(12):5701-9. doi: 10.1128/IAI.00652-09. Epub 2009 Sep 28.
7
Characterisation of PfRON6, a Plasmodium falciparum rhoptry neck protein with a novel cysteine-rich domain.PfRON6,一种富含半胱氨酸的新型 PfRON6 蛋白,是恶性疟原虫(Plasmodium falciparum)裂殖子颈蛋白。
Int J Parasitol. 2009 May;39(6):683-92. doi: 10.1016/j.ijpara.2008.11.002. Epub 2008 Nov 27.
8
Genetically attenuated Plasmodium berghei liver stages persist and elicit sterile protection primarily via CD8 T cells.基因减毒的伯氏疟原虫肝期持续存在,并主要通过CD8 T细胞引发无菌保护。
Am J Pathol. 2007 Jul;171(1):107-15. doi: 10.2353/ajpath.2007.060792.