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1
An expanding toolkit for preclinical pre-erythrocytic malaria vaccine development: bridging traditional mouse malaria models and human trials.用于临床前红细胞前期疟疾疫苗开发的不断扩展的工具包:连接传统小鼠疟疾模型与人体试验
Future Microbiol. 2016 Dec;11(12):1563-1579. doi: 10.2217/fmb-2016-0077. Epub 2016 Nov 18.
2
The species specificity of immunity generated by live whole organism immunisation with erythrocytic and pre-erythrocytic stages of rodent malaria parasites and implications for vaccine development.用红内期和红前期的啮齿动物疟原虫活全生物体免疫产生的免疫的物种特异性及其对疫苗开发的影响。
Int J Parasitol. 2012 Aug;42(9):859-70. doi: 10.1016/j.ijpara.2012.07.001. Epub 2012 Jul 28.
3
Comparative efficacy of pre-erythrocytic whole organism vaccine strategies against the malaria parasite.抗疟原虫红细胞前期全生物体疫苗策略的比较疗效。
Vaccine. 2011 Sep 16;29(40):7002-8. doi: 10.1016/j.vaccine.2011.07.034. Epub 2011 Jul 23.
4
Humanized Mouse Models for the Study of Human Malaria Parasite Biology, Pathogenesis, and Immunity.用于研究人类疟原虫生物学、发病机制和免疫的人源化小鼠模型。
Front Immunol. 2018 Apr 19;9:807. doi: 10.3389/fimmu.2018.00807. eCollection 2018.
5
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.
6
T cell responses to pre-erythrocytic stages of malaria: role in protection and vaccine development against pre-erythrocytic stages.T细胞对疟疾红细胞前期阶段的反应:在针对红细胞前期阶段的保护和疫苗开发中的作用
Annu Rev Immunol. 1993;11:687-727. doi: 10.1146/annurev.iy.11.040193.003351.
7
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.
8
Targeting Plasmodium liver stages: better late than never.靶向疟原虫肝期:亡羊补牢,为时未晚。
Trends Mol Med. 2011 Sep;17(9):527-36. doi: 10.1016/j.molmed.2011.05.008. Epub 2011 Jul 6.
9
Cross-stage immunity for malaria vaccine development.疟疾疫苗开发的跨阶段免疫
Vaccine. 2015 Dec 22;33(52):7513-7. doi: 10.1016/j.vaccine.2015.09.098. Epub 2015 Oct 19.
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Novel approaches to whole sporozoite vaccination against malaria.针对疟疾的全子孢子疫苗接种的新方法。
Vaccine. 2015 Dec 22;33(52):7462-8. doi: 10.1016/j.vaccine.2015.09.095. Epub 2015 Oct 23.

引用本文的文献

1
The origins, isolation, and biological characterization of rodent malaria parasites.啮齿类疟原虫的起源、分离和生物学特性。
Parasitol Int. 2022 Dec;91:102636. doi: 10.1016/j.parint.2022.102636. Epub 2022 Aug 1.
2
Chimeric Plasmodium falciparum parasites expressing Plasmodium vivax circumsporozoite protein fail to produce salivary gland sporozoites.嵌合疟原虫寄生虫表达间日疟原虫环子孢子蛋白未能产生唾液腺孢子。
Malar J. 2018 Aug 9;17(1):288. doi: 10.1186/s12936-018-2431-1.
3
Humanized Mouse Models for the Study of Human Malaria Parasite Biology, Pathogenesis, and Immunity.用于研究人类疟原虫生物学、发病机制和免疫的人源化小鼠模型。
Front Immunol. 2018 Apr 19;9:807. doi: 10.3389/fimmu.2018.00807. eCollection 2018.
4
Humoral protection against mosquito bite-transmitted infection in humanized mice.人源化小鼠中针对蚊媒传播感染的体液免疫保护作用
NPJ Vaccines. 2017 Oct 9;2:27. doi: 10.1038/s41541-017-0028-2. eCollection 2017.
5
An Opsonic Phagocytosis Assay for Plasmodium falciparum Sporozoites.恶性疟原虫子孢子的调理吞噬试验
Clin Vaccine Immunol. 2017 Feb 6;24(2). doi: 10.1128/CVI.00445-16. Print 2017 Feb.

本文引用的文献

1
Seven-Year Efficacy of RTS,S/AS01 Malaria Vaccine among Young African Children.RTS,S/AS01疟疾疫苗在非洲幼儿中的七年疗效
N Engl J Med. 2016 Jun 30;374(26):2519-29. doi: 10.1056/NEJMoa1515257.
2
A highly infectious Plasmodium yoelii parasite, bearing Plasmodium falciparum circumsporozoite protein.一种携带恶性疟原虫环子孢子蛋白的高度传染性约氏疟原虫寄生虫。
Malar J. 2016 Apr 12;15:201. doi: 10.1186/s12936-016-1248-z.
3
Presentation of hepatocellular antigens.肝细胞抗原的呈递。
Cell Mol Immunol. 2016 May;13(3):293-300. doi: 10.1038/cmi.2015.109. Epub 2016 Feb 29.
4
Altered drug susceptibility during host adaptation of a Plasmodium falciparum strain in a non-human primate model.在非人灵长类动物模型中,恶性疟原虫菌株宿主适应性过程中药物敏感性的改变。
Sci Rep. 2016 Feb 16;6:21216. doi: 10.1038/srep21216.
5
Cell based assays for anti-Plasmodium activity evaluation.用于抗疟活性评估的细胞检测法。
Eur J Pharm Sci. 2016 Mar 10;84:26-36. doi: 10.1016/j.ejps.2016.01.001. Epub 2016 Jan 8.
6
The TLR2 is activated by sporozoites and suppresses intrahepatic rodent malaria parasite development.Toll样受体2(TLR2)被子孢子激活,并抑制肝内啮齿动物疟原虫的发育。
Sci Rep. 2015 Dec 15;5:18239. doi: 10.1038/srep18239.
7
The March Toward Malaria Vaccines.迈向疟疾疫苗的征程
Am J Prev Med. 2015 Dec;49(6 Suppl 4):S319-33. doi: 10.1016/j.amepre.2015.09.011.
8
Progress with viral vectored malaria vaccines: A multi-stage approach involving "unnatural immunity".病毒载体疟疾疫苗的进展:一种涉及“非天然免疫”的多阶段方法。
Vaccine. 2015 Dec 22;33(52):7444-51. doi: 10.1016/j.vaccine.2015.09.094. Epub 2015 Oct 21.
9
Humanized Mouse Models to Study Cell-Mediated Immune Responses to Liver-Stage Malaria Vaccines.用于研究针对肝期疟疾疫苗的细胞介导免疫反应的人源化小鼠模型。
Trends Parasitol. 2015 Nov;31(11):583-594. doi: 10.1016/j.pt.2015.06.008. Epub 2015 Oct 11.
10
Assessment of Parasite Liver-Stage Burden in Human-Liver Chimeric Mice.人肝嵌合小鼠中寄生虫肝期负荷的评估
Methods Mol Biol. 2015;1325:59-68. doi: 10.1007/978-1-4939-2815-6_5.

用于临床前红细胞前期疟疾疫苗开发的不断扩展的工具包:连接传统小鼠疟疾模型与人体试验

An expanding toolkit for preclinical pre-erythrocytic malaria vaccine development: bridging traditional mouse malaria models and human trials.

作者信息

Steel Ryan Wj, Kappe Stefan Hi, Sack Brandon K

机构信息

Center for Infectious Disease Research, Formerly Seattle Biomedical Research Institute, 307 Westlake Avenue North, Suite 500, Seattle, WA 98109, USA.

出版信息

Future Microbiol. 2016 Dec;11(12):1563-1579. doi: 10.2217/fmb-2016-0077. Epub 2016 Nov 18.

DOI:10.2217/fmb-2016-0077
PMID:27855488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5131654/
Abstract

Malaria remains a significant public health burden with 214 million new infections and over 400,000 deaths in 2015. Elucidating relevant Plasmodium parasite biology can lead to the identification of novel ways to control and ultimately eliminate the parasite within geographic areas. Particularly, the development of an effective vaccine that targets the clinically silent pre-erythrocytic stages of infection would significantly augment existing malaria elimination tools by preventing both the onset of blood-stage infection/disease as well as spread of the parasite through mosquito transmission. In this Perspective, we discuss the role of small animal models in pre-erythrocytic stage vaccine development, highlighting how human liver-chimeric and human immune system mice are emerging as valuable components of these efforts.

摘要

疟疾仍然是一项重大的公共卫生负担,2015年有2.14亿新感染病例,死亡人数超过40万。阐明疟原虫相关生物学特性有助于找到控制并最终在特定地理区域内消灭该寄生虫的新方法。特别是,开发一种针对临床上无症状的感染前期的有效疫苗,将通过预防血期感染/疾病的发生以及寄生虫通过蚊子传播,显著增强现有的疟疾消除工具。在本综述中,我们讨论了小动物模型在感染前期疫苗开发中的作用,强调了人肝嵌合小鼠和人免疫系统小鼠如何成为这些努力中有价值的组成部分。