2017
DOI: 10.2147/ijn.s114446
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Potential inhibition of HIV-1 encapsidation by oligoribonucleotide–dendrimer nanoparticle complexes

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Cited by 14 publications
(13 citation statements)
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References 59 publications
(72 reference statements)
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“…In addition, high biocompatibility and significant reduction in p24 antigen production was observed in cell culture and intracellularly. 133 In a study by Parboosing et al, 134 RNA decoys in the form of a 16-mer oligoribonucleotide originating from the stem loop 3 of the HIV packaging signal, were attached to dendrimers in an effort to disrupt the packaging process of the HIV life cycle. The results of this study demonstrated efficient delivery into lymphocytes and modest cytoprotective effect against HIV infection.…”
Section: Antiviral Nanotherapeuticsmentioning
confidence: 99%
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“…In addition, high biocompatibility and significant reduction in p24 antigen production was observed in cell culture and intracellularly. 133 In a study by Parboosing et al, 134 RNA decoys in the form of a 16-mer oligoribonucleotide originating from the stem loop 3 of the HIV packaging signal, were attached to dendrimers in an effort to disrupt the packaging process of the HIV life cycle. The results of this study demonstrated efficient delivery into lymphocytes and modest cytoprotective effect against HIV infection.…”
Section: Antiviral Nanotherapeuticsmentioning
confidence: 99%
“…The results of this study demonstrated efficient delivery into lymphocytes and modest cytoprotective effect against HIV infection. 134 Jayant et al, 135 demonstrated that an ARV (tenofovir) and an investigational latency-reversing drug 136 (vorinostat) can be co-encapsulated on ultrasmall (10 ± 3 nm) iron oxide nanoparticles. This research achieved a sustained drug release period (increased by 30%) showing absolute drug release profiles over a 5-day period with simultaneous activation of latent HIV in cultured human astrocytes.…”
Section: Antiviral Nanotherapeuticsmentioning
confidence: 99%
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“…[111][112][113] The antiviral efficiency of nanosystems was a result of viral entry inhibition, activation of CD8 + T cell and/ or antibody mediated response and in some case RNA decoys. 111,113,114 Investigations regarding the efficacy of dendrimers as a nanoperticulated system for designing an antiviral therapy have been introduced by some of the pioneering researches, but their efficiency against NiV is yet to be evaluated.…”
Section: Dendrimersmentioning
confidence: 99%
“…The mechanism of encapsidation, where HIV RNA is packaged into nascent virions, is driven by interactions between by the Gag nucleocapsid protein p7 and a region of the HIV genome known as the packaging signal (Ψ). A decoy RNA, mimicking the Ψ signal, complexed with a third-generation CBS dendrimer was shown to be efficiently delivered to lymphocytes and exerting a cytoprotective effect against HIV, nevertheless, with only a minor suppression of HIV viral load [ 164 , 165 ].…”
Section: Applications Of Dendrimersmentioning
confidence: 99%