Baltimore et al recommend:
In the near term, we recommend that steps be taken to:
1) Strongly discourage, even in those
countries with lax jurisdictions where it might be permitted, any
attempts at germline
genome modification for clinical application in
humans, while societal, environmental, and ethical implications of such
activity
are discussed among scientific and governmental
organizations. (In countries with a highly developed bioscience
capacity,
germline genome modification in humans is currently
illegal or tightly regulated.) This will enable pathways to responsible
uses of this technology, if any, to be identified.
2) Create forums in which experts from
the scientific and bioethics communities can provide information and
education about
this new era of human biology, the issues
accompanying the risks and rewards of using such powerful technology for
a wide
variety of applications including the potential to
treat or cure human genetic disease, and the attendant ethical, social,
and legal implications of genome modification.
3) Encourage and support transparent
research to evaluate the efficacy and specificity of CRISPR-Cas9 genome
engineering technology
in human and nonhuman model systems relevant to its
potential applications for germline gene therapy. Such research is
essential
to inform deliberations about what clinical
applications, if any, might in the future be deemed permissible.
Baltimore et al have a point. Not only can this be significant on a person by person basis but it also has the potential to be weaponiozed. The technology is out there, thousands are now proficient in it, the cost is low and the means for distribution is high.
Clearly a sensible effort in collaboration with others is essential. The problem is that with much of science, the genie is out of the box.