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疟疾寄生虫对树突状细胞- T 细胞相互作用的影响。

The Impact of Malaria Parasites on Dendritic Cell-T Cell Interaction.

机构信息

Institute of Infection, Immunity & Inflammation, University of Glasgow, Glasgow, United Kingdom.

KEMRI-CGMRC/Wellcome Trust Research Programme, Kilifi, Kenya.

出版信息

Front Immunol. 2020 Jul 24;11:1597. doi: 10.3389/fimmu.2020.01597. eCollection 2020.

Abstract

Malaria is caused by apicomplexan parasites of the genus . While infection continues to pose a risk for the majority of the global population, the burden of disease mainly resides in Sub-Saharan Africa. Although immunity develops against disease, this requires years of persistent exposure and is not associated with protection against infection. Repeat infections occur due to the parasite's ability to disrupt or evade the host immune responses. However, despite many years of study, the mechanisms of this disruption remain unclear. Previous studies have demonstrated a parasite-induced failure in dendritic cell (DCs) function affecting the generation of helper T cell responses. These T cells fail to help B cell responses, reducing the production of antibodies that are necessary to control malaria infection. This review focuses on our current understanding of the effect of parasite on DC function, DC-T cell interaction, and T cell activation. A better understanding of how parasites disrupt DC-T cell interactions will lead to new targets and approaches to reinstate adaptive immune responses and enhance parasite immunity.

摘要

疟疾是由疟原虫属的顶复门寄生虫引起的。尽管感染继续对全球大多数人口构成威胁,但疾病负担主要集中在撒哈拉以南非洲地区。虽然人们对疾病产生了免疫力,但这需要多年的持续暴露,而且与防止感染无关。由于寄生虫有能力破坏或逃避宿主的免疫反应,因此会发生重复感染。然而,尽管经过多年的研究,这种破坏的机制仍不清楚。以前的研究表明,寄生虫诱导的树突状细胞 (DC) 功能障碍会影响辅助性 T 细胞反应的产生。这些 T 细胞不能帮助 B 细胞反应,减少了控制疟疾感染所必需的抗体的产生。本综述重点介绍了我们目前对寄生虫对 DC 功能、DC-T 细胞相互作用和 T 细胞激活的影响的理解。更好地了解寄生虫如何破坏 DC-T 细胞相互作用将为恢复适应性免疫反应和增强寄生虫免疫提供新的靶点和方法。

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