Nanomedicine-Based Approaches for mRNA Delivery
Year: 2020
Type: review
Abstract: Messenger RNA (mRNA) has immense potential for developing a wide range of therapies, including immunotherapy and protein replacement. As mRNA presents no risk of integration into the host genome and does not require nuclear entry for transfection, which allows protein production even in nondividing cells, mRNA-based approaches can be envisioned as safe and practical therapeutic strategies. Nevertheless, mRNA presents unfavorable characteristics, such as large size, immunogenicity, limited cellular uptake, and sensitivity to enzymatic degradation, which hinder its use as a therapeutic agent. While mRNA stability and immunogenicity have been ameliorated by direct modifications on the mRNA structure, further improvements in mRNA delivery are still needed for promoting its activity in biological settings. In this regard, nanomedicine has shown the ability for spatiotemporally controlling the function of a myriad of bioactive agents in vivo. Direct engineering of nanomedicine structures for loading, protecting, and releasing mRNA and navigating in biological environments can then be applied for promoting mRNA translation toward the development of effective treatments. Here, we review recent approaches aimed at enhancing mRNA function and its delivery through nanomedicines, with particular emphasis on their applications and eventual clinical translation.
Source: Molecular Pharmaceutics
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Awards: Development of a nano-pharmaceutical strategy for safely and effectively treating pregnant cancer patients, Cancer immunotherapy by in vivo generation of CAR T cells based on targeted mRNA delivery, Development of mRNA drug with RNA type aptamer conferring cell type specific translation activation function, Development of immunostimulatory mRNA and lymphoid tissue-targeting carriers for cancer vaccine, Determination of therapeutic factors using extracellular vesicles secreted from 3D-cultured stem cells
OpenAlex ID: W3080316114
