遗传性疾病治疗中的特定基因组编辑:可能性,进展和前景
Chao Huang1, Qing Li2, Jinsong Li1,2
1Key Laboratory of Systems Health Science of Zhejiang Province, School of Life Science, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou, Zhejiang, China.
Medical review (2021)
|September 19, 2023
概括
基因组编辑为永久修复遗传疾病的DNA提供了新的方法. 本综述涵盖编辑系统及其对状细胞病等遗传性疾病的临床应用.
科学领域:
- 遗传学 遗传学 是一个
- 生物技术是生物技术.
- 分子生物学分子生物学
背景情况:
- 遗传性疾病源于突变,通常无法通过传统方法治疗.
- 基因组编辑技术允许精确的DNA修改.
- 最近的进展显示,治疗遗传性疾病的前景非常好.
研究的目的:
- 审查可编程基因组编辑系统.
- 讨论它们的原则,优点和缺点.
- 突出临床应用和未来方向.
主要方法:
- 对各种基因组编辑系统 (例如,CRISPR-Cas9) 的审查.
- 分析它们的机制,优势和局限性.
- 对遗传性疾病的临床试验数据的检查.
主要成果:
- 基因组编辑系统在治疗遗传疾病方面取得了重大进展.
- 临床应用包括状细胞病,β - thalassemia,LCA和HeFH.
- 活体和体内体质编辑显示出希望,而生殖系编辑面临挑战.
结论:
- 基因组编辑是治疗遗传疾病的强大工具.
- 需要在交付,切割和维修方面取得进一步的进步.
- 体细胞编辑具有很大的治疗潜力.
相关概念视频
CRISPR
52.2K
Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
52.2K
What is Genetic Engineering?
74.3K
Overview
74.3K
Conservative Site-specific Recombination and Phase Variation
6.0K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
The recognition sites for Cre recombinase called LoxP...
6.0K
Gene Therapy
25.5K
Gene therapy is a technique where a gene is inserted into a person’s cells to prevent or treat a serious disease. The added gene may be a healthy version of the gene that is mutated in the patient, or it could be a different gene that inactivates or compensates for the patient’s disease-causing gene. For example, in patients with severe combined immunodeficiency (SCID) due to a mutation in the gene for the enzyme adenosine deaminase, a functioning version of the gene can be...
25.5K
CRISPR/Cas9 Genome Editing
48
The CRISPR-Cas system serves as a bacterial defense mechanism against invading genetic elements such as viruses and plasmids, forming the foundation for its adaptation as a powerful genome-editing tool. Originally discovered in prokaryotes, this system has been repurposed to revolutionize genetic engineering across a wide range of organisms, including plants, animals, and humans. The core component, Cas9, is an endonuclease derived from Streptococcus pyogenes, capable of introducing...
48
Microorganisms in Medicine and Therapeutics
53
Microorganisms play a fundamental role in vaccine development, gene therapy, and therapeutic production. Their biological properties are harnessed to advance medicine and public health. Beyond immunization, microorganisms contribute to gut health, antibiotic synthesis, and genetic disease treatment.Live Attenuated and Inactivated VaccinesLive attenuated vaccines, such as the measles, mumps, and rubella (MMR) vaccine, utilize weakened forms of pathogens to closely resemble natural infections.
53


