Genetic protection modifications: Moving beyond the binary distinction between therapy and enhancement for human genome editing

Research output: Contribution to journalJournal articlepeer-review

The current debate and policy surrounding the use of genome editing in humans typically relies on a binary distinction between therapy and human enhancement. Here, we argue that this dichotomy fails to take into account perhaps the most significant potential uses of CRISPR-Cas9 genome editing in humans. We argue that genetic treatment of sporadic Alzheimer's disease, breast and ovarian cancer predisposing BRCA1/2 mutations, and the introduction of human immunodeficiency virus resistance in humans should be considered within a new category of genetic protection treatments. We suggest that if this category is not introduced, life-altering research might be unnecessarily limited by current or future policy. Otherwise ad hoc decisions might be made, which introduce a risk of unforeseen moral costs, and might overlook or fail to address some important opportunities.
Original languageEnglish
JournalCRISPR Journal
Volume2
Issue number6
Pages (from-to)362-369
Number of pages8
ISSN2573-1599
DOIs
Publication statusPublished - 2019

ID: 233589263