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Vaccines against tropical parasitic diseases: a persisting answer to a persisting problem.针对热带寄生虫病的疫苗:持久应对持久问题的答案。
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[The immunological aspects of tropical malaria related to the development of an antimalarial vaccine].[与抗疟疫苗研发相关的热带疟疾免疫学方面]
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Overview: immunology of malaria and progress in malaria vaccine development.概述:疟疾免疫学与疟疾疫苗研发进展
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本文引用的文献

1
Protective CD8+ T-cell immunity to human malaria induced by chimpanzee adenovirus-MVA immunisation. chimpanzee 腺病毒-MVA 免疫诱导的对人疟疾的保护性 CD8+ T 细胞免疫。
Nat Commun. 2013;4:2836. doi: 10.1038/ncomms3836.
2
Short-lived effector CD8 T cells induced by genetically attenuated malaria parasite vaccination express CD11c.经基因减毒疟原虫疫苗接种诱导的寿命短的效应性 CD8 T 细胞表达 CD11c。
Infect Immun. 2013 Nov;81(11):4171-81. doi: 10.1128/IAI.00871-13. Epub 2013 Aug 26.
3
Protection against malaria by intravenous immunization with a nonreplicating sporozoite vaccine.经静脉免疫接种非复制性疟原虫疫苗预防疟疾。
Science. 2013 Sep 20;341(6152):1359-65. doi: 10.1126/science.1241800. Epub 2013 Aug 8.
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New vaccines for neglected parasitic diseases and dengue.新型疫苗可预防被忽视的寄生虫病和登革热。
Transl Res. 2013 Sep;162(3):144-55. doi: 10.1016/j.trsl.2013.03.006. Epub 2013 Apr 8.
5
CD4+ T cell persistence and function after infection are maintained by low-level peptide:MHC class II presentation.感染后 CD4+ T 细胞的持久性和功能由低水平的肽:MHC Ⅱ类呈递维持。
J Immunol. 2013 Mar 15;190(6):2828-34. doi: 10.4049/jimmunol.1202183. Epub 2013 Feb 4.
6
Peripheral tissue surveillance and residency by memory T cells.记忆 T 细胞对周围组织的监测和驻留。
Trends Immunol. 2013 Jan;34(1):27-32. doi: 10.1016/j.it.2012.08.008. Epub 2012 Oct 2.
7
Immunological memory ≠ protective immunity.免疫记忆≠保护性免疫。
Cell Mol Life Sci. 2012 May;69(10):1635-40. doi: 10.1007/s00018-012-0972-y. Epub 2012 Apr 6.
8
Vaccines against malaria.疟疾疫苗。
Philos Trans R Soc Lond B Biol Sci. 2011 Oct 12;366(1579):2806-14. doi: 10.1098/rstb.2011.0091.
9
Induction and maintenance of protective CD8+ T cells against malaria liver stages: implications for vaccine development.诱导和维持针对疟疾肝期的保护性 CD8+ T 细胞:对疫苗开发的启示。
Mem Inst Oswaldo Cruz. 2011 Aug;106 Suppl 1(0 1):172-8. doi: 10.1590/s0074-02762011000900022.
10
Long-term protection against malaria after experimental sporozoite inoculation: an open-label follow-up study.实验性疟原虫接种后对疟疾的长期保护作用:一项开放性随访研究。
Lancet. 2011 May 21;377(9779):1770-6. doi: 10.1016/S0140-6736(11)60360-7. Epub 2011 Apr 22.

针对热带寄生虫病的疫苗:持久应对持久问题的答案。

Vaccines against tropical parasitic diseases: a persisting answer to a persisting problem.

机构信息

Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

Nat Immunol. 2014 May;15(5):403-5. doi: 10.1038/ni.2853.

DOI:10.1038/ni.2853
PMID:24747701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4814932/
Abstract

Live and live-attenuated whole organism vaccines against malaria and cutaneous leishmaniasis due to remain the most uniformly effective vaccines against human parasitic diseases. These vaccines are discussed in terms of the nature of the T cell populations that mediate the strong and durable localized immunity to these infections, and the requirement for persisting antigen to generate and maintain the protective response. The difficulties in developing subunit vaccines that fulfill this requirement argue that despite their own formidable problems in manufacture and delivery, live and live- attenuated whole organism vaccines against human parasitic diseases should be vigorously pursued.

摘要

针对疟疾和皮肤利什曼病的活疫苗和减毒活疫苗仍然是针对人体寄生虫病最有效、最普遍的疫苗。本文将讨论介导针对这些感染的强烈和持久局部免疫的 T 细胞群体的性质,以及产生和维持保护反应所需的持续抗原。开发符合这一要求的亚单位疫苗存在困难,这表明,尽管活疫苗和减毒活疫苗在制造和使用方面存在自身的巨大问题,但仍应大力研究针对人体寄生虫病的活疫苗和减毒活疫苗。