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DC-SIGN:丙型肝炎病毒的结合受体

DC-SIGN: binding receptors for hepatitis C virus.

作者信息

Wang Quan-Chu, Feng Zhi-Hua, Nie Qing-He, Zhou Yong-Xing

机构信息

PLA Center for Diagnosis and Treatment for Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an 710038, China.

出版信息

Chin Med J (Engl). 2004 Sep;117(9):1395-400.

Abstract

OBJECTIVE

To review the recent developments in and research into binding receptors of hepatitis C virus (HCV) and especially the role of dendritic cell-specific adhesion receptor (DC-SIGN) in HCV.

DATA SOURCES

Both Chinese- and English-language literature was searched using MEDLINE (2000 - 2003) and the databank of Chinese-language literature (2000 - 2003).

STUDY SELECTION

Relevant articles on DC-SIGN and HCV binding receptors in recent domestic and foreign literature were selected.

DATA EXTRACTION

Data were mainly extracted from 40 articles which are listed in the references section of this review.

RESULTS

DC-SIGN, a dendritic cell-specific adhesion receptor and a type II transmembrane mannose-binding C-type lectin, is very important in the function of dendritic cells (DC), both in mediating naïve T cell interactions through ICAM-3 and as a rolling receptor that mediates the DC-specific ICAM-2-dependent migration processes. It can be used by HCV and other viral and bacterial pathogens including human immunodeficiency virus (HIV), Ebola virus, CMV and Mycobacterium tuberculosis to facilitate infection. Both DC-SIGN and DC-SIGNR can act either in cis, by concentrating virus on target cells, or in trans, by transmission of bound virus to a target cell expressing appropriate entry receptors. Recent report showed that DC-SIGN not only plays a role in entry into DC, HCV E2 interaction with DC-SIGN might also be detrimental to the interaction of DC with T cells during antigen presentation.

CONCLUSIONS

DC-SIGNs are high-affinity binding receptors for HCV. The clinical strategies that target DC-SIGN may be successful in restricting HCV dissemination and pathogenesis as well as directing the migration of DCs to manipulate appropriate immune responses in autoimmunity and tumorigenic situations.

摘要

目的

综述丙型肝炎病毒(HCV)结合受体的研究进展,尤其是树突状细胞特异性粘附受体(DC-SIGN)在HCV中的作用。

资料来源

使用MEDLINE(2000 - 2003年)及中文文献数据库(2000 - 2003年)检索中英文文献。

研究选择

选取国内外近期有关DC-SIGN与HCV结合受体的相关文章。

资料提取

资料主要从本综述参考文献部分列出的40篇文章中提取。

结果

DC-SIGN是一种树突状细胞特异性粘附受体,属于II型跨膜甘露糖结合C型凝集素,在树突状细胞(DC)功能中非常重要,它既能通过细胞间粘附分子-3(ICAM-3)介导幼稚T细胞相互作用,又作为一种滚动受体介导DC特异性的依赖ICAM-2的迁移过程。HCV以及包括人类免疫缺陷病毒(HIV)、埃博拉病毒、巨细胞病毒(CMV)和结核分枝杆菌在内的其他病毒及细菌病原体均可利用它促进感染。DC-SIGN和DC-SIGNR既能通过将病毒聚集在靶细胞上发挥顺式作用,也能通过将结合的病毒传递给表达合适进入受体的靶细胞发挥反式作用。近期报道显示,DC-SIGN不仅在HCV进入DC过程中发挥作用,HCV E2与DC-SIGN的相互作用在抗原呈递过程中可能也不利于DC与T细胞的相互作用。

结论

DC-SIGN是HCV的高亲和力结合受体。针对DC-SIGN的临床策略可能成功限制HCV传播和发病机制,以及在自身免疫和肿瘤发生情况下引导DC迁移以调控适当的免疫反应。

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