Mechanisms for Cell-to-Cell Transmission of HIV-1

被引:116
作者
Bracq, Lucie [1 ,2 ,3 ,4 ,5 ]
Xie, Maorong [1 ,2 ,3 ,5 ]
Benichou, Serge [1 ,2 ,3 ,4 ,5 ]
Bouchet, Jerome [1 ,2 ,3 ,5 ]
机构
[1] Inst Cochin, INSERM, U1016, Paris, France
[2] CNRS, UMR8104, Paris, France
[3] Univ Paris 05, Sorbonne Paris Cite, Paris, France
[4] Chinese Acad Sci, Inst Pasteur Shanghai, Int Associated Lab LIA VirHost, Shanghai, Peoples R China
[5] Univ Paris 05, Inst Pasteur, CNRS, Int Associated Lab LIA VirHost, Paris, France
关键词
HIV-1; cell-to-cell transfer; macrophages; dendritic cells; T cells; HUMAN-IMMUNODEFICIENCY-VIRUS; MULTINUCLEATED GIANT-CELLS; MATURE DENDRITIC CELLS; HTLV-III/LAV ENVELOPE; VIROLOGICAL SYNAPSE; MEMBRANE NANOTUBES; PLASMA-MEMBRANE; TUNNELING NANOTUBES; INFECTIOUS SYNAPSE; DC-SIGN;
D O I
10.3389/fimmu.2018.00260
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
While HIV-1 infection of target cells with cell-free viral particles has been largely documented, intercellular transmission through direct cell-to-cell contact may be a predominant mode of propagation in host. To spread, HIV-1 infects cells of the immune system and takes advantage of their specific particularities and functions. Subversion of intercellular communication allows to improve HIV-1 replication through a multiplicity of intercellular structures and membrane protrusions, like tunneling nanotubes, filopodia, or lamellipodia-like structures involved in the formation of the virological synapse. Other features of immune cells, like the immunological synapse or the phagocytosis of infected cells are hijacked by HIV-1 and used as gateways to infect target cells. Finally, HIV-1 reuses its fusogenic capacity to provoke fusion between infected donor cells and target cells, and to form infected syncytia with high capacity of viral production and improved capacities of motility or survival. All these modes of cell-to-cell transfer are now considered as viral mechanisms to escape immune system and antiretroviral therapies, and could be involved in the establishment of persistent virus reservoirs in different host tissues.
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页数:14
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