2018
DOI: 10.1016/j.jconrel.2018.03.035
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Preclinical evaluation of mRNA trimannosylated lipopolyplexes as therapeutic cancer vaccines targeting dendritic cells

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Cited by 96 publications
(100 citation statements)
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“…Journal of Controlled Release 303 (2019) carried cargos. In studies relevant to the in vivo characteristics, fluorescent materials are often employed as a label for tracking the behaviour of liposomes in the body [128]. However, this hardly provides a strong evidence to verify the carrier integrity, since fluorescent materials may aggregate to emit light even after carrier collapse.…”
Section: Ag Release and Liposome Integrity In Vivomentioning
confidence: 99%
“…Journal of Controlled Release 303 (2019) carried cargos. In studies relevant to the in vivo characteristics, fluorescent materials are often employed as a label for tracking the behaviour of liposomes in the body [128]. However, this hardly provides a strong evidence to verify the carrier integrity, since fluorescent materials may aggregate to emit light even after carrier collapse.…”
Section: Ag Release and Liposome Integrity In Vivomentioning
confidence: 99%
“…By contrast, non‐viral vectors have no such major concerns as a result of their higher safety, especially for direct in vivo administration . In addition, they comprises more flexible tools for the loading and delivery of various types of genes, including RNA and DNA of different sizes . It is possible to rationally design novel non‐viral vectors with a high transfection efficiency and controlled gene delivery based on a deeper understanding of both physiopathological processes and gene therapy approaches.…”
Section: Discussionmentioning
confidence: 99%
“…43,44 In addition, they comprises more flexible tools for the loading and delivery of various types of genes, including RNA and DNA of different sizes. 45,46 It…”
Section: Delivery Vectorsmentioning
confidence: 99%
“…More recently, a lipid–polymer–ribonucleic acid (RNA) lipoplex (LPR) modified with a tri‐antenna of α‐ d ‐mannopyranoside (triMN‐LPR) was evaluated for efficient delivery of mRNA to DCs . Because the mannose receptors are expressed on the surface membrane of DCs and macrophages,[123b] mannose was utilized to enhance the binding affinity of the LPR to DCs.…”
Section: Application Of Polymeric Nanomedicine To Cancer Immunotherapymentioning
confidence: 99%
“…It is well‐known that cationic liposomes and polymers can protect the mRNA against RNases . Under consideration that whether positively charged lipid‐based formulations are accumulated into major organs such as liver and lungs, the triMN functionalization method would endow the synergistic effect to various types of mRNA‐based vaccines which are already known as safe vaccination strategy in some clinical trials …”
Section: Application Of Polymeric Nanomedicine To Cancer Immunotherapymentioning
confidence: 99%