Gene-Edited Stem Cells for Ischemic Vascular Disease: Current Advances and Future Perspectives

Ischemic vascular diseases remain a leading cause of morbidity and mortality worldwide and are frequently associated with irreversible tissue damage. Although stem cell-based therapies have shown promise for vascular regeneration, their clinical translation has been limited by poor survival, insufficient engraftment, functional heterogeneity, and immune rejection. Recent advances in genome-editing technologies, including CRISPR/Cas9, base editing, and prime editing, have provided powerful tools for overcoming these limitations through precise genetic modification of stem cells. Gene editing can enhance angiogenic potential, improve resistance to ischemic stress, augment paracrine activity, promote endothelial maturation, and reduce immunogenicity. In this review, we outline the current genome-editing toolbox and its application to stem cell engineering for vascular regeneration in ischemic disease. We also examine emerging therapeutic concepts, universal donor cell platforms, and key issues in safety and ethics, with a focus on translational pathways. Taken together, advances at the interface of genome editing and stem cell biology are likely to accelerate the development of regenerative therapies that deliver more durable vascular repair in ischemic vascular disease.

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Publication Details

Journal
Current Issues in Molecular Biology
Published
2026-07-02
DOI
https://doi.org/10.3390/cimb48070681
Primary Topic
CRISPR and Genetic Engineering
Type
article
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article

Gene-Edited Stem Cells for Ischemic Vascular Disease: Current Advances and Future Perspectives

Sung-Whan Kim, Seongho Han
Current Issues in Molecular Biology
CRISPR and Genetic Engineering
article

Gene-Edited Stem Cells for Ischemic Vascular Disease: Current Advances and Future Perspectives

Sung-Whan Kim, Seongho Han
article en

Abstract

Ischemic vascular diseases remain a leading cause of morbidity and mortality worldwide and are frequently associated with irreversible tissue damage. Although stem cell-based therapies have shown promise for vascular regeneration, their clinical translation has been limited by poor survival, insufficient engraftment, functional heterogeneity, and immune rejection. Recent advances in genome-editing technologies, including CRISPR/Cas9, base editing, and prime editing, have provided powerful tools for overcoming these limitations through precise genetic modification of stem cells. Gene editing can enhance angiogenic potential, improve resistance to ischemic stress, augment paracrine activity, promote endothelial maturation, and reduce immunogenicity. In this review, we outline the current genome-editing toolbox and its application to stem cell engineering for vascular regeneration in ischemic disease. We also examine emerging therapeutic concepts, universal donor cell platforms, and key issues in safety and ethics, with a focus on translational pathways. Taken together, advances at the interface of genome editing and stem cell biology are likely to accelerate the development of regenerative therapies that deliver more durable vascular repair in ischemic vascular disease.

Current Issues in Molecular BiologyVol. 48(7)
Catholic Kwandong University International St. Mary's Hospital (KR), Dong-A University (KR), Catholic Kwandong University (KR)
Openalex Percentile: Top 12%
CRISPR and Genetic Engineering
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