±«Óătv the authors: is a Research Professor in Philosophy at ±«Óătv University. is Associate Professor in Medicine at the University of Cape Town.
In July 2021, after more than two years of study and consultation, the released three reports: , a and on human genome editing.
The governance framework lists a number ethical values and principles, many of which have not been included in previous international reports on human genome editing. The commitments to inclusiveness, fairness, social justice, non-discrimination, solidarity and global health justice inform the content of all three reports.
The committee also addressed research involving both somatic and germline human genome editing.
Somatic human genome editing involves making changes to the DNA of non-reproductive cells. The therapeutic aim is to correct mutations responsible for genetic disease. Germline human genome editing involves making changes to the DNA of reproductive cells. These changes become heritable when the genetically altered cells are used for reproduction. For many, heritable human genome editing is ethically contentious because of its impact on future generations.
As members of the WHO Expert Advisory, we appreciate the challenges in moving forward with human genome editing technology, given our commitment to ensure that this is not just personalized medicine for an elite few.
Access and equity
Early in the committee’s deliberations, Francis Collins, director of the National Institutes of Health in the United States, suggested that attention focused on anything other than heritable human genome editing research was a “.” The WHO did not share this perspective, as reflected in the mandate given to the expert advisory committee.
For the most part, the committee elected to side-step the debate on the permissibility of heritable human genome editing and focus more broadly on issues of access and equity. On advice from the committee, WHO Director-General Tedros Adhanom Ghebreyesus stated that “.”
To improve access to information about clinical trials involving somatic human genome editing and to promote equitable access to the potential benefits of research, in August 2019 the committee launched the . This is a publicly accessible database currently in a pilot phase.
Sickle cell disease
Several potential therapies using somatic genome editing are in development, with some currently in clinical trials.
Sickle cell disease is an extremely painful, debilitating disease that currently can only be managed, not cured. The red blood cells of people with sickle cell disease are shaped in the form of a sickle and tend to clog up small veins, interrupting the blood flow to parts of the body and causing excruciating pain.
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Sickle cell disease is particularly common in areas of the world that have had a high burden of malaria — at least partly because having one gene for sickle cell disease protects against severe malaria. The and is particularly high in parts of Africa and India. Because of global migration — for instance during the transatlantic slave trade - .
Because sickle cell disease is a genetic condition linked to one mutation, it lends itself well to somatic genome editing. Several clinical trials are now under way (see the WHO genome editing registry for examples) and . The challenge, however, is that future safe and effective genome editing therapies are likely to be expensive and unlikely to be available to most people with sickle cell disease in Africa or India for many years to come.
Ethical challenges
The human data and materials that scientists use to develop and test new therapies comes mostly from . A direct consequence of this is that innovative therapies are often untested or less well tested in women or people from different ethnic and racial groups. For example, in people of African ancestry in the United States, based on genetic risk factors that predict this disease in white people.
Much of the scientific work leading to therapeutic innovations occurs with fewer resource constraints, strong health-care systems and stable infrastructure. As a consequence, .
Somatic genome editing interventions risk becoming solidly intertwined with corporate interest and profit motives. This is partly because , increasing the cost for others wanting to use practices or materials for therapy design or delivery.
Fostering innovation
The WHO governance framework emphasizes ensuring that genome editing therapies are developed and made available equitably, and inclusive of global human genetic diversity. It also encourages critically analyzing the effects of proprietary ownership of genome editing technologies and future therapies.
As well, equitable access means fostering innovation in low- and middle-income countries. An example is the based at the University of the Witwatersrand in South Africa. This research team investigates and seeks to develop gene therapy approaches — including genome editing — to alleviate the high burden of hepatitis B.
The WHO framework recommends that somatic genome editing clinical trials not be conducted in countries without effective research regulation and oversight. It also discourages trials in countries where the resultant therapies are likely to be so expensive or require such specialist care, that they are unlikely ever to be made available. Specifically, this means that clinical trials for somatic genome editing innovations should only be conducted in countries where it’s likely that the innovation would be marketed, and where there is robust ethics oversight.
Somatic human genome editing research offers previously unimaginable pathways to alleviating suffering for millions of people living with conditions such as sickle cell disease. Unless specific attention is paid to ensuring the development of affordable innovations that can be implemented across the globe, these benefits may never reach the global poor.
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