Abstract
Since the creation of the first transgenic animals four decades ago, a wide ethical consensus has been reached that in contrast to a somatic gene therapy, germline gene interventions in humans are not to be allowed. Legislation in many countries reflects this consensus but this ethical taboo has recently been challenged. First, by the decision of the British Parliament to allow fertility clinics to carry out mitochondrial replacements in February 2015 and second, by the announcement of Chinese scientists in April 2015 that they had already edited germline genes in non-viable human embryos by CRISPR-Cas9 technology. The CRISPR-Cas 9 is a revolutionary new technology for a targeted editing of DNA – effective, cheap and easy to use. Until recently, unintended off-target changes in the genome caused by classical genetic engineering technologies were seen as a major safety obstacle for using them for human germline modifications. The very recent rapid progress in increasing the precision of genome editing by CRISPR-Cas 9 in order to minimize off-target changes will bring the technology in the near future to the acceptable safety level ready to use for clinical trials, but only in those cases when a mutant, disease causing DNA sequence is corrected to a healthy wild-type.
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This work was supported by the Slovak Research and Development Agency under the contract No. APVV-0379-12.
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Sýkora, P. (2018). Chapter 11 Germline Gene Therapy in the Era of Precise Genome Editing: How Far Should We Go?. In: Soniewicka, M. (eds) The Ethics of Reproductive Genetics. Philosophy and Medicine, vol 128. Springer, Cham. https://doi.org/10.1007/978-3-319-60684-2_11
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