在β-血病基因疗法的进展:CRISPR/Cas系统和交付创新

Hongmei Liu1,2, Peng Zhang1

  • 1Center for Tissue Engineering and Stem Cell Research, Key Laboratory of Functional Nucleic Acids-Based Biopharmaceutical Research, Guizhou Biomanufacturing Laboratory, Guizhou Medical University, Guiyang 550031, China.

Cells
|October 28, 2025
PubMed
概括

克里斯普尔基因编辑通过纠正HBB基因突变或提高胎儿血红蛋白,为beta-thalassemia提供了新的希望. 有效和安全的输送方法对于这些先进疗法的成功临床转化至关重要.

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