Genome editing: an ethical review
Genome editing techniques are now widely used in research across many areas of human health. In this section we look at basic research, and the prospects for treating disease, avoiding genetic diseases, and human enhancement. We explore the extent to which this raises new and distinctive ethical questions, and offers new perspectives on questions that have been discussed in the past.
Understanding human health through research
Health research often involves the use of animal models, such as mice, to investigate the causes of human disease and to study biological processes such as embryo development. Genome editing tools have enabled research techniques such as gene ‘knockout’ (deleting a gene to study its function in living organisms) to proceed more quickly, cheaply, and with greater precision. It has also made it easier to alter or insert DNA sequences, and to make several alterations at the same time.
Ethically significant research possibilities raised by genome editing include:
- Bringing basic research and its translation into treatment closer together, since alteration of a gene could serve both to discover its function and to enable treatment of a disease caused by that gene.
- A potential increase in the use of larger animals, such as primates, in disease research, as they may offer better ‘models’ for studying certain diseases than, for example, mice.
- Using genetically altered animals to study the effects of gene mutations that are specific to a family or individual, introducing a direct connection between an animal model and an individual patient.
Potentially increased rates of experimentation, facilitated by genome editing, may prompt a number of additional concerns for some people, including:
- The possible consequences of an increased demand for the use of human embryos for research involving genome editing.
- The risk of scientific publishing and communication moving too slowly to keep pace with experimentation, meaning a lack of coordination among research groups and duplication of work, which may in turn have consequences such as unnecessary increases in the number of animals used in research.
Genome editing might have a transformative impact in many areas of medicine. Three areas in particular are:
Cell-based therapies, e.g. transplanting genome-edited white blood cells into patients to attack HIV infection or blood cancers such as leukaemia and lymphoma.
Gene therapy, e.g. to correct mutations that cause genetic diseases in particular tissues or organs, such as muscular dystrophy.
Xenotransplantation (transplantation of organs from one species to another), e.g. from pigs to humans, where the pig cells have been altered to prevent the transmission of viruses.
As with any new treatment, there will be questions over the safety of the technique, whether it is likely to work, and whether it should be offered as an alternative or replacement for current treatment options. The main safety consideration with genome editing in patients is the possibility of unintended effects due to off-target DNA alterations. Given concerns over the uncertainty of outcomes, a relevant consideration will be whether alterations to the genome in patients’ tissues can be neutralised or reversed.
Avoiding genetic disease
There are more than 4,000 known, inherited, single-gene conditions, which, collectively, are thought to affect at least one per cent of the world’s population. The use of genome editing in reproductive treatments could prevent the transmission of some of these conditions (e.g. thalassaemia or cystic fibrosis) to future generations, by making changes to the DNA of a very early stage embryo that will be replicated in all cells in the body as it grows.
Genome editing may offer an alternative approach to familial disease prevention, especially in certain (albeit rare) cases where established methods such as pre-implantation genetic diagnosis (PGD) would not be effective.
Many people have concerns about the possible use of genome editing in human reproduction, for example, about the implications of making genetic changes that will be passed on to future generations.
Whether it is offered as an ‘alternative’ reproductive treatment depends not only on the outcomes, risks, costs, etc., but also on other factors including how reproductive choice is valued, and the extent of society’s interest in people’s choices and welfare, which may, in turn, have consequences for governance and regulation.
Genetic variations may not always directly cause disease, but may be associated with an increased risk of developing a certain disease or, conversely, have a protective effect against a certain disease. For example, a recent laboratory trial of genome editing of preimplantation human embryos reported the introduction of a gene variant offering protection against HIV.
Genome editing also raises the possibility of ‘engineering’ humans with desirable genetic traits, for example to suit specific environmental conditions or to enhance athletic ability.
A much discussed issue is how to distinguish between acceptable and unacceptable uses of genome editing.
There are concerns that the use of genome editing may facilitate the spread of ‘consumer’ or ‘liberal’ eugenics, driven primarily by the choices of parents, which could, in turn, exacerbate divisions or inequalities in society. Some people may also be ethically opposed to the practice of pre-determining a person’s genetic characteristics, arguing that this constrains their future choices in unacceptable ways.