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Unlocking the Therapeutic Applicability of LNP-mRNA: Chemistry, Formulation, and Clinical Strategies.

作者信息

Huang Xiaonan, Ma Yishan, Ma Guanghui, Xia Yufei

机构信息

Sinovac Biotech Ltd., Beijing, PR China.

State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, PR China.

出版信息

Research (Wash D C). 2024 Jun 18;7:0370. doi: 10.34133/research.0370. eCollection 2024.


DOI:10.34133/research.0370
PMID:38894715
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11185168/
Abstract

Messenger RNA (mRNA) has emerged as an innovative therapeutic modality, offering promising avenues for the prevention and treatment of a variety of diseases. The tremendous success of mRNA vaccines in effectively combatting coronavirus disease 2019 (COVID-19) evidences the unlimited medical and therapeutic potential of mRNA technology. Overcoming challenges related to mRNA stability, immunogenicity, and precision targeting has been made possible by recent advancements in lipid nanoparticles (LNPs). This review summarizes state-of-the-art LNP-mRNA-based therapeutics, including their structure, material compositions, design guidelines, and screening principles. Additionally, we highlight current preclinical and clinical trends in LNP-mRNA therapeutics in a broad range of treatments in ophthalmological conditions, cancer immunotherapy, gene editing, and rare-disease medicine. Particular attention is given to the translation and evolution of LNP-mRNA vaccines into a broader spectrum of therapeutics. We explore concerns in the aspects of inadequate extrahepatic targeting efficacy, elevated doses, safety concerns, and challenges of large-scale production procedures. This discussion may offer insights and perspectives on near- and long-term clinical development prospects for LNP-mRNA therapeutics.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/56c963ea5e58/research.0370.fig.011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/b42861598a86/research.0370.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/961c1cf30002/research.0370.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/420c99921d2e/research.0370.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/4ac7269ca706/research.0370.fig.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/b8a065591c7c/research.0370.fig.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/cc336fd45561/research.0370.fig.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/1d98734962d0/research.0370.fig.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/1e8d21c45f9a/research.0370.fig.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/2429b6de80a5/research.0370.fig.009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/99cab19fb286/research.0370.fig.010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/56c963ea5e58/research.0370.fig.011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/b42861598a86/research.0370.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/961c1cf30002/research.0370.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/420c99921d2e/research.0370.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/4ac7269ca706/research.0370.fig.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/b8a065591c7c/research.0370.fig.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/cc336fd45561/research.0370.fig.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/1d98734962d0/research.0370.fig.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/1e8d21c45f9a/research.0370.fig.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/2429b6de80a5/research.0370.fig.009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/99cab19fb286/research.0370.fig.010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eafd/11185168/56c963ea5e58/research.0370.fig.011.jpg

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本文引用的文献

[1]
Thiophene-based lipids for mRNA delivery to pulmonary and retinal tissues.

Proc Natl Acad Sci U S A. 2024-3-12

[2]
High-throughput barcoding of nanoparticles identifies cationic, degradable lipid-like materials for mRNA delivery to the lungs in female preclinical models.

Nat Commun. 2024-2-29

[3]
Antigen Presenting Cell Mimetic Lipid Nanoparticles for Rapid mRNA CAR T Cell Cancer Immunotherapy.

Adv Mater. 2024-6

[4]
Chemistry and Art of Developing Lipid Nanoparticles for Biologics Delivery: Focus on Development and Scale-Up.

Pharmaceutics. 2024-1-19

[5]
mRNA vaccine trafficking and resulting protein expression after intramuscular administration.

Mol Ther Nucleic Acids. 2023-11-24

[6]
Unleashing the Potential: Designing Antibody-Targeted Lipid Nanoparticles for Industrial Applications with CMC Considerations and Clinical Outlook.

Mol Pharm. 2024-1-1

[7]
Drug delivery systems for CRISPR-based genome editors.

Nat Rev Drug Discov. 2023-11

[8]
Regulatory perspective for quality evaluation of lipid nanoparticle-based mRNA vaccines in China.

Biologicals. 2023-11

[9]
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Proc Natl Acad Sci U S A. 2023-8-15

[10]
CMC Strategies and Advanced Technologies for Vaccine Development to Boost Acceleration and Pandemic Preparedness.

Vaccines (Basel). 2023-6-26

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