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Review
. 2021 Jan:168:3-29.
doi: 10.1016/j.addr.2019.11.005. Epub 2019 Nov 21.

Rational designs of in vivo CRISPR-Cas delivery systems

Affiliations
Review

Rational designs of in vivo CRISPR-Cas delivery systems

Cong-Fei Xu et al. Adv Drug Deliv Rev. 2021 Jan.

Abstract

The CRISPR-Cas system initiated a revolution in genome editing when it was, for the first time, demonstrated success in the mammalian cells. Today, scientists are able to readily edit genomes, regulate gene transcription, engineer posttranscriptional events, and image nucleic acids using CRISPR-Cas-based tools. However, to efficiently transport CRISPR-Cas into target tissues/cells remains challenging due to many extra- and intra-cellular barriers, therefore largely limiting the applications of CRISPR-based therapeutics in vivo. In this review, we summarize the features of plasmid-, RNA- and ribonucleoprotein (RNP)-based CRISPR-Cas therapeutics. Then, we survey the current in vivo delivery systems. We specify the requirements for efficient in vivo delivery in clinical settings, and highlight both efficiency and safety for different CRISPR-Cas tools.

Keywords: CRISPR-Cas; Drug delivery; Genome editing; Nanomedicine.

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