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bioRxiv · 10.1101/2022.10.14.512310

Non-viral gene editing in utero with lipid nanoparticles complexed to mRNA

Gao, K.·Li, J.·Song, H.·Han, H.·Wang, Y.·Yin, B.·Farmer, D. L.·Murthy, N.·Wang, A.
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Abstract

Nanoparticle-based drug delivery systems have the potential to revolutionize medicine but their low vascular permeability and rapid clearance by phagocytic cells have limited their medical impact. Nanoparticles delivered at the in utero stage have the potential to overcome these key limitations, due to the high rate of angiogenesis and cell division in fetal tissue, and the under-developed immune system. However, very little is known about nanoparticle drug delivery at the fetal stage of development. In this report, using Ai9 CRE reporter mice, we demonstrate that lipid nanoparticle (LNP) mRNA complexes can deliver mRNA for gene editing enzymes in utero after an intrahepatic injection, and can access and edit major organs, such as the heart, the liver, kidneys, lungs and the gastrointestinal tract with remarkable efficiency and low toxicity. In addition, we show here that Cas9 mRNA and sgRNA complexed to LNPs were able to edit the fetal organs in utero after an intrahepatic injection. These experiments demonstrate the possibility of non-viral delivery of gene editing enzymes in utero and nanoparticle drug delivery has great potential for delivering macromolecules to organs outside of the liver in utero, which provides a promising strategy for treating a wide variety of devastating genetic diseases before birth.

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Gao, K., Li, J., Song, H., Han, H., Wang, Y., Yin, B., Farmer, D. L., Murthy, N., Wang, A.. 2022-10-16. Non-viral gene editing in utero with lipid nanoparticles complexed to mRNA. https://doi.org/10.1101/2022.10.14.512310

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