학술논문

The NIH Somatic Cell Genome Editing program
Document Type
article
Source
Nature. 592(7853)
Subject
Biological Sciences
Biomedical and Clinical Sciences
Genetics
Stem Cell Research - Embryonic - Human
Biotechnology
Stem Cell Research
Human Genome
Generic health relevance
Animals
Cells
Gene Editing
Genetic Therapy
Genome
Human
Goals
Humans
National Institutes of Health (U.S.)
United States
SCGE Consortium
General Science & Technology
Language
Abstract
The move from reading to writing the human genome offers new opportunities to improve human health. The United States National Institutes of Health (NIH) Somatic Cell Genome Editing (SCGE) Consortium aims to accelerate the development of safer and more-effective methods to edit the genomes of disease-relevant somatic cells in patients, even in tissues that are difficult to reach. Here we discuss the consortium's plans to develop and benchmark approaches to induce and measure genome modifications, and to define downstream functional consequences of genome editing within human cells. Central to this effort is a rigorous and innovative approach that requires validation of the technology through third-party testing in small and large animals. New genome editors, delivery technologies and methods for tracking edited cells in vivo, as well as newly developed animal models and human biological systems, will be assembled-along with validated datasets-into an SCGE Toolkit, which will be disseminated widely to the biomedical research community. We visualize this toolkit-and the knowledge generated by its applications-as a means to accelerate the clinical development of new therapies for a wide range of conditions.