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免疫调节对疟原虫的影响:来自小鼠模型的血液阶段疟疾疫苗设计的启示。

Regulation of immunity to Plasmodium: implications from mouse models for blood stage malaria vaccine design.

机构信息

Institute of Molecular and Cellular Biology, University of Leeds, Clarendon Way, Leeds LS2 9JT, United Kingdom.

出版信息

Exp Parasitol. 2010 Nov;126(3):406-14. doi: 10.1016/j.exppara.2010.01.028. Epub 2010 Feb 6.

DOI:10.1016/j.exppara.2010.01.028
PMID:20138874
Abstract

Malaria, a disease caused by the protozoan parasite Plasmodium, remains a serious healthcare problem in developing countries worldwide. While the host-parasite relationship in humans has been difficult to determine, the pliability of murine malaria models has enabled valuable contributions to the understanding of the pathogenesis of disease. Although no single model reflects precisely malaria infection of the human, different models collectively provide important information on the mechanisms of protective immunity and immunopathogenesis. This review summarizes progress towards understanding the broad spectrum of immune responsiveness to the blood stages of the malaria parasite during experimental infections in mice and highlights how examination of murine malarias sheds light on the factors involved in the modulation of vaccine-potentiated immunity.

摘要

疟疾是一种由原生动物寄生虫疟原虫引起的疾病,在世界范围内的发展中国家仍然是一个严重的医疗保健问题。虽然人类的宿主-寄生虫关系很难确定,但鼠疟模型的可变性使得对疾病发病机制的理解做出了有价值的贡献。虽然没有单一的模型能准确反映人类疟疾感染,但不同的模型共同提供了关于保护性免疫和免疫发病机制的重要信息。这篇综述总结了在实验性感染小鼠的血液阶段疟原虫过程中,对广泛的免疫反应的理解所取得的进展,并强调了检查鼠疟如何揭示了调节疫苗增强免疫的因素。

相似文献

1
Regulation of immunity to Plasmodium: implications from mouse models for blood stage malaria vaccine design.免疫调节对疟原虫的影响:来自小鼠模型的血液阶段疟疾疫苗设计的启示。
Exp Parasitol. 2010 Nov;126(3):406-14. doi: 10.1016/j.exppara.2010.01.028. Epub 2010 Feb 6.
2
What have we learnt from mouse models for the study of malaria?我们从用于疟疾研究的小鼠模型中学到了什么?
Eur J Immunol. 2009 Aug;39(8):2004-7. doi: 10.1002/eji.200939552.
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Towards a blood-stage vaccine for malaria: are we following all the leads?迈向疟疾血液阶段疫苗:我们是否追踪了所有线索?
Nat Rev Immunol. 2001 Nov;1(2):117-25. doi: 10.1038/35100540.
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Antigen presentation and dendritic cell biology in malaria.疟疾中的抗原呈递与树突状细胞生物学
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IL-12 and NK cells are required for antigen-specific adaptive immunity against malaria initiated by CD8+ T cells in the Plasmodium yoelii model.在约氏疟原虫模型中,IL-12和自然杀伤细胞是由CD8 + T细胞引发的针对疟疾的抗原特异性适应性免疫所必需的。
J Immunol. 1999 Jul 15;163(2):884-92.
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Plasmodium berghei XAT: contribution of gammadelta T cells to host defense against infection with blood-stage nonlethal malaria parasite.伯氏疟原虫XAT:γδT细胞在宿主抵御血液期非致死性疟原虫感染中的作用
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J Immunol. 1989 Sep 15;143(6):2017-23.
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Exoerythrocytic malaria vaccine development: understanding host-parasite immunobiology underscores strategic success.红细胞外期疟疾疫苗的研发:理解宿主-寄生虫免疫生物学是战略成功的关键。
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Malaria blood-stage infection and its control by the immune system.疟疾血液阶段感染及其免疫系统的控制。
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引用本文的文献

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Neddylation contributes to CD4+ T cell-mediated protective immunity against blood-stage Plasmodium infection.泛素化修饰有助于 CD4+ T 细胞介导的抗疟原虫血期感染的保护性免疫。
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Avian malaria and bird humoral immune response.
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Malar J. 2016 Nov 4;15(1):531. doi: 10.1186/s12936-016-1579-9.
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Malaria-Cutaneous Leishmaniasis Co-infection: Influence on Disease Outcomes and Immune Response.疟疾-皮肤利什曼病合并感染:对疾病结局和免疫反应的影响。
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Novel approaches to identify protective malaria vaccine candidates.探索鉴定保护性疟疾疫苗候选物的新方法。
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