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利什曼病中的巨噬细胞极化:拓宽视野。

Macrophage Polarization in Leishmaniasis: Broadening Horizons.

机构信息

Biosciences and Biotechnology Postgraduate Program, Carlos Chagas Institute (ICC), Fiocruz, Curitiba, Brazil.

Laboratory of Immunoparasitology, Department of Pathological Sciences, State University of Londrina, Londrina, Brazil.

出版信息

Front Immunol. 2018 Oct 31;9:2529. doi: 10.3389/fimmu.2018.02529. eCollection 2018.

Abstract

Leishmaniasis is a vector-borne neglected tropical disease that affects more than 700,000 people annually. parasites cause the disease, and different species trigger a distinct immune response and clinical manifestations. Macrophages are the final host cells for the proliferation of parasites, and these cells are the key to a controlled or exacerbated response that culminates in clinical manifestations. M1 and M2 are the two main macrophage phenotypes. M1 is a pro-inflammatory subtype with microbicidal properties, and M2, or alternatively activated, is an anti-inflammatory/regulatory subtype that is related to inflammation resolution and tissue repair. The present review elucidates the roles of M1 and M2 polarization in leishmaniasis and highlights the role of the salivary components of the vector and the action of the parasite in the macrophage plasticity.

摘要

利什曼病是一种由寄生虫引起的经媒介传播的被忽视的热带病,每年影响超过 70 万人。不同的寄生虫会引发不同的免疫反应和临床表现。巨噬细胞是寄生虫增殖的最终宿主细胞,这些细胞是控制或加剧反应的关键,最终导致临床表现。M1 和 M2 是两种主要的巨噬细胞表型。M1 是一种具有杀菌特性的促炎亚型,而 M2 或替代性激活的则是一种抗炎/调节亚型,与炎症消退和组织修复有关。本综述阐明了 M1 和 M2 极化在利什曼病中的作用,并强调了媒介的唾液成分和寄生虫在巨噬细胞可塑性中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3d/6220043/c8ffb737cadb/fimmu-09-02529-g0001.jpg

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