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Nucleic Acid Ther. 2018 Jun;28(3):146-157. doi: 10.1089/nat.2018.0721. Epub 2018 Apr 23.

Lipid Nanoparticles Enabling Gene Therapies: From Concepts to Clinical Utility.

Author information

1
1 Department of Biochemistry and Molecular Biology, University of British Columbia , Vancouver, British Columbia, Canada .
2
2 Department of Clinical Chemistry and Haematology, University Medical Center Utrecht , Utrecht, the Netherlands .

Abstract

Genetic drugs based on RNA or DNA have remarkable therapeutic potential as virtually any disease can be treated by silencing a pathological gene, expressing a beneficial protein, or by editing defective genes. However, therapies based on nucleic acid polymers require sophisticated delivery systems to deliver these macromolecules to the interior of target cells. In this study, we review progress in developing nonviral lipid nanoparticle (LNP) delivery systems that have attractive properties, including ease of manufacture, reduced immune responses, multidosing capabilities, larger payloads, and flexibility of design. LNP systems represent the most advanced delivery systems for genetic drugs as it is expected that an LNP-short interfering RNA (siRNA) formulation will receive clinical approval from the Food and Drug Administration (FDA) in 2018 for treatment of the hereditary condition transthyretin-mediated amyloidosis, a fatal condition for which there is currently no treatment. This achievement is largely due to the development of optimized ionizable cationic lipids, arguably the most important factor in the clinical success of LNP-siRNA. In addition, we highlight potential LNP applications, including targeting tissues beyond the liver and therapeutic approaches based on messenger RNA or Clustered Regularly Interspaced Short Palindromic Repeats/Cas.

KEYWORDS:

drug delivery; gene therapy; genetic drugs; ionizable cationic lipid; lipid nanoparticle; nucleic acid

PMID:
29683383
DOI:
10.1089/nat.2018.0721
[Indexed for MEDLINE]

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