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趋化因子在淋巴细胞招募到肝脏中的作用。

The role of chemokines in the recruitment of lymphocytes to the liver.

机构信息

Centre for Liver Research, 5th Floor, Institute of Biomedical Research, University of Birmingham, Wolfson Drive, Edgbaston, Birmingham B15 2TT, UK.

出版信息

J Autoimmun. 2010 Feb;34(1):45-54. doi: 10.1016/j.jaut.2009.07.011. Epub 2009 Sep 9.

Abstract

Chemokines direct leukocyte trafficking and positioning within tissues. They thus play critical roles in regulating immune responses and inflammation. The chemokine system is complex involving interactions between multiple chemokines and their receptors that operate in combinatorial cascades with adhesion molecules. The involvement of multiple chemokines and chemokine receptors in these processes brings flexibility and specificity to recruitment. The hepatic vascular bed is a unique low flow environment through which leukocyte are recruited to the liver during homeostatic immune surveillance and in response to infection or injury. The rate of leukocyte recruitment and the nature of cells recruited through the sinusoids in response to inflammatory signals will shape the severity of disease. At one end of the spectrum fulminant liver failure results from a rapid recruitment of leukocytes that leads to hepatocyte destruction and liver failure at the other diseases such as chronic hepatitis C infection may progress over many years from hepatitis to fibrosis and cirrhosis. Chronic hepatitis is charactezised by a T lymphocyte rich infiltrate and the nature and outcome of hepatitis will depend on the T cell subsets recruited, their activation and function within the liver. Different subsets of effector T cells have been described based on their secretion of cytokines and specific functions. These include Th1 and Th2 cells and more recently Th17 and Th9 cells which are associated with different types of immune response and which express distinct patterns of chemokine receptors that promote their recruitment under particular conditions. The effector function of these cells is balanced by the recruitment of regulatory T cells that are able to suppress antigen-specific effectors to allow resolution of immune responses and restoration of immune homeostasis. Understanding the signals that are responsible for recruiting different lymphocyte subsets to the liver will elucidate disease pathogenesis and open up new therapeutic approaches to modulate recruitment in favour of resolution rather than injury.

摘要

趋化因子指导白细胞在组织中的迁移和定位。因此,它们在调节免疫反应和炎症中起着关键作用。趋化因子系统很复杂,涉及多种趋化因子及其受体之间的相互作用,这些作用通过黏附分子以组合级联的方式进行。多种趋化因子和趋化因子受体的参与为募集带来了灵活性和特异性。在这些过程中,多个趋化因子和趋化因子受体的参与为募集带来了灵活性和特异性。肝脏血管床是一个独特的低流量环境,白细胞在稳态免疫监测期间以及响应感染或损伤时被募集到肝脏。白细胞通过窦状隙募集的速度和募集的细胞类型将决定疾病的严重程度。在一端,暴发性肝衰竭是由于白细胞的快速募集导致的,这导致肝细胞破坏和肝功能衰竭;在另一端,慢性丙型肝炎感染等疾病可能会在多年内从肝炎发展为纤维化和肝硬化。慢性肝炎的特征是富含 T 淋巴细胞的浸润,肝炎的性质和结局将取决于募集的 T 细胞亚群、它们在肝脏内的激活和功能。根据其细胞因子的分泌和特定功能,已经描述了不同的效应 T 细胞亚群。这些包括 Th1 和 Th2 细胞,以及最近的 Th17 和 Th9 细胞,它们与不同类型的免疫反应相关联,并表达促进其在特定条件下募集的独特趋化因子受体模式。这些细胞的效应功能通过调节性 T 细胞的募集来平衡,调节性 T 细胞能够抑制抗原特异性效应器,从而允许免疫反应的解决和免疫稳态的恢复。了解负责将不同淋巴细胞亚群募集到肝脏的信号将阐明疾病的发病机制,并开辟新的治疗方法来调节募集,以利于解决而不是损伤。

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