High-throughput CRISPR technology: a novel horizon for solid organ transplantation

Front Immunol. 2024 Jan 4:14:1295523. doi: 10.3389/fimmu.2023.1295523. eCollection 2023.

Abstract

Organ transplantation is the gold standard therapy for end-stage organ failure. However, the shortage of available grafts and long-term graft dysfunction remain the primary barriers to organ transplantation. Exploring approaches to solve these issues is urgent, and CRISPR/Cas9-based transcriptome editing provides one potential solution. Furthermore, combining CRISPR/Cas9-based gene editing with an ex vivo organ perfusion system would enable pre-implantation transcriptome editing of grafts. How to determine effective intervention targets becomes a new problem. Fortunately, the advent of high-throughput CRISPR screening has dramatically accelerated the effective targets. This review summarizes the current advancements, utilization, and workflow of CRISPR screening in various immune and non-immune cells. It also discusses the ongoing applications of CRISPR/Cas-based gene editing in transplantation and the prospective applications of CRISPR screening in solid organ transplantation.

Keywords: CRISPR screening; CRISPR/Cas9; high-throughput; solid organ transplantation; transcriptome editing.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • CRISPR-Cas Systems*
  • Gene Editing*

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by Fundamental Research Funds for the Central Universities [2021GCRC037 to JX, and YCJJ20230232 to SR], the National Natural Science Foundation of China [82241217 and 82071803 to JW, 82271811, 82170504, and 81730015 to JX], the project funded by China Postdoctoral Science Foundation [2021M691155 to JY, and 2023M741285 to XZ], and the Science foundation of union hospital [2021xhyn096 to JY].