Ethical and Welfare Implications of Genetically Altered Non-Human Primates for Biomedical Research
Abstract Breakthroughs in gene editing technologies have made it feasible to create genetically altered ( GA ) non-human primate ( NHP ) models of disease. This area of research is accelerating, particularly in China, Japan and the USA, and could lead to an increase in NHP use globally. The hope is...
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| Format: | Electronic Article |
| Language: | English |
| Check availability: | HBZ Gateway |
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| Fernleihe: | Fernleihe für die Fachinformationsdienste |
| Published: |
Brill
2020
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| In: |
Journal of applied animal ethics research
Year: 2020, Volume: 2, Issue: 2, Pages: 151-176 |
| Further subjects: | B
macaque
B Ethics B transgenesis B genetically modified B transgenic B Animal welfare B marmoset B gene editing |
| Online Access: |
Volltext (kostenfrei) Volltext (kostenfrei) |
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| 520 | |a Abstract Breakthroughs in gene editing technologies have made it feasible to create genetically altered ( GA ) non-human primate ( NHP ) models of disease. This area of research is accelerating, particularly in China, Japan and the USA, and could lead to an increase in NHP use globally. The hope is that genetic models in animal species closely related to humans will significantly improve understanding of neurological diseases and validation of potential therapeutic interventions, for which there is a dire need. However, the creation and use of GA NHP s raises serious animal welfare and ethical issues, which are highlighted here. It represents a step change in how these highly sentient animals are used in biomedical research, because of the large numbers required, inherent wastage and the sum of the harms caused to the animals involved. There is little evidence of these important issues being addressed alongside the rapidly advancing science. We are still learning about how gene editing tools work in NHP s, and significant added scientific and medical benefit from GA NHP models has yet to be demonstrated. Together, this suggests that current regulatory and review frameworks, in some jurisdictions at least, are not adequately equipped to deal with this emerging, complex area of NHP use. | ||
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