髓系 C 型凝集素受体在宿主-病原体相互作用和基于聚糖的靶向中的作用

IF 6.9 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Current Opinion in Chemical Biology Pub Date : 2024-08-29 DOI:10.1016/j.cbpa.2024.102521
Felix Stegmann , Bernd Lepenies
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引用次数: 0

摘要

凝集素与糖的相互作用在免疫系统中起着至关重要的作用。髓系 C 型凝集素受体(CLR)是先天性免疫系统中的一类重要凝集素。髓系 C 型凝集素受体是一种模式识别受体,主要由髓系细胞(如巨噬细胞、树突状细胞和中性粒细胞)表达。在先天性免疫中,CLRs 有助于自我/非自我识别。虽然 CLRs 识别病原体相关分子模式(PAMPs)可能有助于保护性免疫反应,但病原体也可能利用 CLRs 参与免疫逃避。由于各种 CLR 可作为内细胞受体并触发髓系细胞中不同的信号通路,因此 CLR 靶向已被证明可用于将药物/抗原递送至抗原递呈细胞并调节免疫反应。本综述涵盖了过去两年中病原体/CLR相互作用的最新发现以及CLR靶向的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Myeloid C-type lectin receptors in host–pathogen interactions and glycan-based targeting

Lectin–glycan interactions play a crucial role in the immune system. An important class of lectins in the innate immune system is myeloid C-type lectin receptors (CLRs). Myeloid CLRs act as pattern recognition receptors and are predominantly expressed by myeloid cells, such as macrophages, dendritic cells, and neutrophils. In innate immunity, CLRs contribute to self/non-self discrimination. While the recognition of pathogen-associated molecular patterns (PAMPs) by CLRs may contribute to a protective immune response, CLR engagement can also be exploited by pathogens for immune evasion. Since various CLRs act as endocytic receptors and trigger distinct signaling pathways in myeloid cells, CLR targeting has proven useful for drug/antigen delivery into antigen-presenting cells and the modulation of immune responses. This review covers recent discoveries of pathogen/CLR interactions and novel approaches for CLR targeting within the period of the past two years.

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来源期刊
Current Opinion in Chemical Biology
Current Opinion in Chemical Biology 生物-生化与分子生物学
CiteScore
13.30
自引率
1.30%
发文量
113
审稿时长
74 days
期刊介绍: COCHBI (Current Opinion in Chemical Biology) is a systematic review journal designed to offer specialists a unique and educational platform. Its goal is to help professionals stay informed about the growing volume of information in the field of Chemical Biology through systematic reviews.
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