Interplay between HIV-1 innate sensing and restriction in mucosal dendritic cells: balancing defense and viral transmission

被引:9
|
作者
Hertoghs, Nina [1 ]
Geijtenbeek, Teunis B. H. [1 ]
Ribeiro, Carla M. S. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Expt Immunol, Amsterdam, Netherlands
基金
欧洲研究理事会;
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; SIGN-MEDIATED INTERNALIZATION; SUMO-INTERACTING MOTIFS; GMP-AMP SYNTHASE; DC-SIGN; LANGERHANS CELLS; TRIM5-ALPHA RESTRICTION; RETROVIRUS RESTRICTION; IMMUNE SENSOR; MEASLES-VIRUS;
D O I
10.1016/j.coviro.2017.01.001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Innate sensing of HIV-1 by dendritic cells (DCs) initiates cell intrinsic signalling programs that direct virus restriction and antiviral defenses. These responses include the production of type I interferon (IFN) and a large number of IFN-stimulated genes (ISGs) with a broad spectrum of antiviral effector functions. Initial interactions of HIV-1 at the mucosal surfaces with DC-expressed innate immune factors including cGAS, TRIM5a and SAMHD1 are predictive of viraemia, inflammation and disease pathogenesis. Here, we review the molecular basis of HIV-1 sensing in the two major mucosal DC subsets, that is, epithelial Langerhans cells and subepithelial CD11c+ conventional DCs. We discuss the concerted actions of the host restriction factors and innate sensors as well as viral evasion mechanisms in determining HIV-1 susceptibility to infection and directing antiviral adaptive immune responses.
引用
收藏
页码:112 / 119
页数:8
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