2017
DOI: 10.21037/atm.2017.06.34
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An immunoregulatory role of dendritic cell-derived exosomes versus HIV-1 infection: take it easy but be warned

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Cited by 5 publications
(5 citation statements)
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References 62 publications
(79 reference statements)
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“…In particular, EXOs are characterized by a defined content of proteins, RNAs, and microRNAs that are released into target cells and have the potential to modulate several pathological scenarios, including the maintenance of tumor microenvironment [19]. In DCs, the role of exosomes in cellular and humoral immune activation is well recognized, while less is known for the role of MVs [20][21][22]. The significance of IGFBP-6 associated with EVs in immune regulation will be the focus of further studies.…”
Section: Discussionmentioning
confidence: 99%
“…In particular, EXOs are characterized by a defined content of proteins, RNAs, and microRNAs that are released into target cells and have the potential to modulate several pathological scenarios, including the maintenance of tumor microenvironment [19]. In DCs, the role of exosomes in cellular and humoral immune activation is well recognized, while less is known for the role of MVs [20][21][22]. The significance of IGFBP-6 associated with EVs in immune regulation will be the focus of further studies.…”
Section: Discussionmentioning
confidence: 99%
“…All of the above processes allow HIV to inhibit the antiviral effects of type I IFN by inhibiting Vif-mediated STAT1 and STAT3, which consequently reduces the induction of the ISG-15 protein by IFN-α. Multiple mechanisms, which may be cell-specific, may explain the therapeutic failure of type I IFN in the course of HIV infection [ 201 , 202 , 203 ]. In addition, HIV can block the induction of type II and III IFNs in human dendritic cells and macrophages as a result of inhibition of the phosphorylation process of TANK1 binding kinase (TBK1) [ 204 ].…”
Section: Resultsmentioning
confidence: 99%
“…This leads to activation mediated by gp120 and lymphocyte function-associated antigen 1 (LFA-1) that initiates signal transduction by inducing T-cell entrapment and activation ( 32 , 33 ). The interaction between DCs and T cells allows trapped HIV-1 particles to reach target T cells in a manner similar to that established in DCs, wherein DCs can capture ganglioside-rich exosomes ( 34 ). It has been shown that increasing numbers of viruses can bind directly to integrins ( 35 ).…”
Section: Spread Of Virus In the Immune Systemmentioning
confidence: 99%