The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Germline genome editing versus preimplantation genetic diagnosis: Is there a case in favour of germline interventions?
Abstract
CRISPR is widely considered to be a disruptive technology. However, when it comes to the most controversial topic, germline genome editing (GGE), there is no consensus on whether this technology has any substantial advantages over existing procedures such as embryo selection after in vitro fertilization (IVF) and preimplantation genetic diagnosis (PGD). Answering this question, however, is crucial for evaluating whether the pursuit of further research and development on GGE is justified. This paper explores the question from both a clinical and a moral viewpoint, namely whether GGE has any advantages over existing technologies of selective reproduction and whether GGE could complement or even replace them. In a first step, I review an argument of extended applicability. The paper confirms that there are some scenarios in which only germline intervention allows couples to have (biologically related) healthy offspring, because selection will not avoid disease. In a second step, I examine possible moral arguments in favour of genetic modification, namely that GGE could save some embryos and that GGE would provide certain benefits for a future person that PGD does not. Both arguments for GGE have limitations. With regard to the extended applicability of GGE, however, a weak case in favour of GGE should still be made.
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“Only in very few cases (e.g., when both parents are homozygous for an autosomal recessive disease) would HGE be the only option to prevent the transmission of a monogenetic disease (Ranisch 2020a).”
From Initial heritable genome editing: mapping a responsible pathway from basic research to the clinic (2023) · cites this paper as Ranisch 2020a
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“However, it remains an open question whether any HGE could benefit (in case of success) or harm (in case of failure) the future person (Ranisch 2020a), or whether it is neutral to the future person created”
From Initial heritable genome editing: mapping a responsible pathway from basic research to the clinic (2023) · cites this paper as Ranisch 2020a
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“However, in most cases, preimplantation genetic testing (PGT) and embryo selection is an alternative to preventing the transmission of diseases.”
From Initial heritable genome editing: mapping a responsible pathway from basic research to the clinic (2023) · cites this paper as Ranisch 2020a
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Citations
Cites
Correction of a pathogenic gene mutation in human embryos
Ma, H., Marti-Gutierrez, N., Park, S.-W., Wu, J., Lee, Y., Suzuki, K., Koski, A., Ji, D., Hayama, T., Ahmed, R., et al. (2017) · Nature · doi:10.1038/nature23305 · Cited by 992
Molecular remission of infant B-ALL after infusion of universal TALEN gene-edited CAR T cells
Qasim, W., Zhan, H., Samarasinghe, S., Adams, S., Amrolia, P., Stafford, S., Butler, K., Rivat, C., Wright, G., Somana, K., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aaj2013 · Cited by 902
Genome editing reveals a role for OCT4 in human embryogenesis
Fogarty, N. M. E., McCarthy, A., Snijders, K. E., Powell, B. E., Kubikova, N., Blakeley, P., Lea, R., Elder, K., Wamaitha, S. E., Kim, D., et al. (2017) · Nature · doi:10.1038/nature24033 · Cited by 392
A New Class of Medicines through DNA Editing
Porteus, M. H. (2019) · New England Journal of Medicine · doi:10.1056/nejmra1800729 · Cited by 229
Inter-homologue repair in fertilized human eggs?
Egli, D., Zuccaro, M. V., Kosicki, M., Church, G. M., Bradley, A., & Jasin, M. (2018) · Nature · doi:10.1038/s41586-018-0379-5 · Cited by 111
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Sorted by citations
Initial heritable genome editing: mapping a responsible pathway from basic research to the clinic
Ranisch, R., Trettenbach, K., & Arnason, G. (2023) · Medicine, Health Care and Philosophy · doi:10.1007/s11019-022-10115-x · Cited by 19
Self-citation
Metadata
- Authors
- Ranisch, R.
- Venue
- Bioethics
- Publisher
- Wiley
- Published
- 2019-08-25
- Volume
- 34
- Issue
- 1
- Pages
- 60-69
- ISSN
- 0269-9702
- 1467-8519
- PMC
- PMC6973094
- Cited by
- 48
- References
- 5
- Language
- en
- Funders
- Bundesministerium für Bildung und Forschung (01GP1680)
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