HIV endocytosis after dendritic cell to T cell viral transfer leads to productive virus infection

被引:27
作者
Clotet-Codina, Imma [1 ]
Bosch, Berta [1 ]
Senserrich, Jordi [1 ]
Teresa Fernandez-Figueras, Maria [2 ]
Pena, Ruth [1 ]
Ballana, Ester [1 ]
Bofill, Margarita [1 ]
Clotet, Bonaventura [1 ]
Este, Jose A. [1 ]
机构
[1] Univ Autonoma Barcelona, Retrovirol Lab IrsiCaixa, Hosp Univ Germans Trias & Pujol, Badalona 08916, Spain
[2] Univ Autonoma Barcelona, Dept Pathol, Hosp Univ Germans Trias & Pujol, Badalona 08916, Spain
基金
美国国家卫生研究院;
关键词
HIV entry; Dendritic cell; Entry inhibitor; Virus transfer; HUMAN-IMMUNODEFICIENCY-VIRUS; DC-SIGN; TYPE-1; INFECTION; VIROLOGICAL SYNAPSES; TRANSMISSION; MATURATION; ENTRY; LYMPHOCYTES; INHIBITION; EXPRESSION;
D O I
10.1016/j.antiviral.2009.03.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Contacts between HIV-producing T cells and primary CD4+ T cells may induce the uptake of HIV by target cells that are endocytosed into trypsin-resistant compartments. We have now compared the mechanism of virus transmission from T cell-to-T cell versus infected dendritic cells (DCs)-to-T cell. In cocultures of HIV-1-infected DCs with primary CD4+ T cells, virus transmission to the target cells was resistant to trypsin treatment and could only be prevented by the anti-SUgp120 antibody IgGb12 but not by TAK-779, C34 or AZT. Importantly, upon stimulation of purified HIV-1-loaded CD4+ T cells with PHA/IL-2, cells became productively infected as measured by intracellular CAp24 staining and antigen determination in the cell supernatant. These results suggest that the viral endocytic transfer may represent a escape mechanism in the presence of drugs targeting HIV-1 entry or the host immune system. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:94 / 98
页数:5
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