体基因疗法的生物伦理:我们到目前为止知道了什么?
Paola Buedo1, Alahi Bianchini2, Katarzyna Klas1
1Research Ethics in Medicine Study Group (REMEDY), Jagiellonian University Medical College, Krakow, Poland.
Current medical research and opinion
|September 29, 2023
概括
这一系统性审查映射了围绕体基因治疗的生物伦理论点. 它确定了189个不同的论点,分为与研究相关的和与社会相关的关注点,以告知未来的伦理讨论.
科学领域:
- 生物伦理学生物伦理学
- 基因治疗 基因治疗
- 科学文献综述 科学文献综述
背景情况:
- 体基因疗法带来了复杂的伦理挑战.
- 需要对生物伦理辩论进行系统的概述.
- 了解论点对于规范性分析至关重要.
研究的目的:
- 系统地审查和分类有关体质基因疗法的生物伦理论点.
- 创建一个全面的伦理挑战和观点数据库.
- 促进对体基因疗法的规范分析和公共话语.
主要方法:
- 使用Strech和Sofaer方法进行系统的文献综述.
- 包括来自主要学术数据库 (PubMed,Lilacs,PhilPapers,Google Scholar) 的 217 篇出版物.
- 用于数据分析和论证分类的元合成.
主要成果:
- 189个不同的生物伦理论点的提取和分类.
- 论点分为23个类别:12个与研究相关 (例如风险/益处,同意) 和11个与社会相关 (例如人口影响,人类身份).
- 在体基因疗法研究和应用中确定关键的伦理挑战.
结论:
- 这项工作为正在进行的关于体质基因疗法的伦理和社会维度的讨论做出了贡献.
- 这些发现可以作为未来规范性伦理分析的基础.
- 对生物伦理论据的全面理解对于负责任的基因治疗的开发和应用至关重要.
更多相关视频
07:43Author Spotlight: Addressing Regulatory Gaps in Molecular Studies by Quantifying Viral Vectors in Complex Matrices
Published on: July 14, 2023
2.0K
05:08Targeted and Selective Treatment of Pluripotent Stem Cell-derived Teratomas Using External Beam Radiation in a Small-animal Model
Published on: February 17, 2019
6.2K
相关概念视频
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
What is Genetic Engineering?
74.3K
Overview
74.3K
Somatic to iPS Cell Reprogramming
2.2K
Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012...
2.2K
Induced Pluripotent Stem Cells
4.1K
Stem cells are undifferentiated cells that divide and produce different cell types. Ordinarily, cells that have differentiated into a specific cell type are terminally differentiated; however, scientists have found a way to reprogram these mature cells so that they dedifferentiate and return to an unspecialized, proliferative state. These cells are pluripotent like embryonic stem cells—able to produce all cell types—and are called induced pluripotent stem cells (iPSCs).
Somatic...
Somatic...
4.1K
CRISPR
52.1K
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...
52.1K
Methods of Nuclear Reprogramming
1.8K
Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for...
1.8K
