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Recommendation
1512 (2001)[1]
Protection
of the human genome by the Council of Europe
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The Council of Europe?s Parliamentary Assembly notes that the
human genome international research project, in view of the numerous
and unimaginable consequences that it might have for medicine and
for the animal and plant world, conjures up scenarios for all
humanity that raise numerous ethical questions, while holding out
the promise of enormous improvements in the quality of life.
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The protection of human dignity should be the guiding principle for
the handling of the Human Genome Project.
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The genetic age will dawn with the completion of the project:
diagnosis will become objective, and it will be possible to identify
the presence of genetic disorders or a genetic predisposition to
illnesses at an early stage. In many cases, gene therapy will become
possible, and this will basically give rise to a form of genetic
engineering designed, for instance, to avoid the development of a
tumour in an individual found to be at risk. It might also be
applied to other illnesses, such as hypertension, diabetes,
Alzheimer?s disease, osteoporosis, certain psychiatric disorders,
etc.
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At the same time, the Assembly is aware of the enormous ethical
implications of further research on the human genome, including some
of a negative nature. These include questions regarding the cloning
of cells, the conditions ruling genetic testing and the divulging
and use of obtained information.
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In this connection, the Assembly is fully aware of the now
well-known fact that laboratories, with their associated databanks,
are already actively at work on DNA separation in certain European
countries and enjoy the financial support of prominent
pharmaceutical companies.
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The Assembly is also aware that substantial economic interests are
at stake in the Human Genome Project, by virtue of the very fact
that it might hold out incalculable opportunities for preventing
illness and improving treatment, as it involves many public and
private research centres to which considerable financial resources
will be allocated.
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The Assembly is of the opinion that the results of this grandiose
research effort ? in which the United States has the lead over
Europe ? must be made available to all, genetic information being
a common human heritage, as set out in Article 1 of the Universal
Declaration on the Human Genome and Human Rights, adopted at Unesco
in Paris on 11 November 1997. The Assembly in particular
refers in this context to the Council of Europe Convention for the
Protection of Human Rights and Dignity of the Human Being with
regard to the Application of Biology and Medicine ? Convention on
Human Rights and Biomedicine (ETS No. 164) as well as its own
Recommendations 1425 (1999) on biotechnology and
intellectual property and 1468 (2000) on biotechnologies.
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In particular, the Assembly is aware that the prospects opened up by
the discoveries associated with the Human Genome Project pose a
whole series of ethical problems, essentially concerning such
fundamental issues as the use of genetic information for preventive
purposes and possibly a presumed right, at a later stage, to take
preventive action when certain genetic information is obtained.
However, a crucial question will be the assessment of who will have
which rights to use the information: the case of insurance
companies, employers, parents, schools, etc.
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The Assembly calls, inter
alia, through the establishment of a Euroforum on Human Genetics,
for the widest possible participation by citizens in the discussion
on the human genome through the involvement of the European media
and suitable and accurate information by the Council of
Europe.
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The Assembly expresses the wish that the scope of action of the
above-mentioned authority should not be confined to Europe, but that
it may become part of a world authority under the aegis of the
United Nations. To this end, the Assembly advocates that the
necessary contacts be established with the appropriate bodies within
the UN and Unesco as soon as possible.
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In view of the above, the Assembly recommends that the Committee of
Ministers:
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invite every Council of Europe member state concerned to set up,
under its own domestic legislation, a national authority having
the express task of monitoring, informing and advising on the
compliance of research on the human genome with universally
recognised ethical and moral principles of respect for life and
human dignity;
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set up, at European level as well, and more specifically in the
context of the Council of Europe, a body or authority to fulfill
on a permanent basis the task of monitoring the development of
the Human Genome Project research process, ensuring respect for
ethical principles in the context of research on the human
genome, assessing the effects of such research also regarding
health risks, and giving thorough consideration to all the
ethical aspects of the project, and consider in this context the
role of the Steering Committee on Bioethics (CDBI);
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ensure that these bodies for monitoring research on the human
genome will familiarise the European public with new
possibilities for progress in genetics in terms of information
and technology and serve also to promote campaigns to inform and
educate the public, in particular the health professions;
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make sure that consultation of the European authority be
mandatory, and that it formulate an opinion when conventions are
drafted on this subject in the context of the Council of Europe
and codes of ethics produced; such a body should also have free
access to important information on genetics and be able to carry
out its own inspections of public and private European research
institutes;
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ask member states to sign, ratify and implement the Convention
on Human Rights and Biomedicine;
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ask all Council of Europe member states to strive to change the
basis of patent law in international fora, as far as the
ownership of human being tissue and genes is concerned, into law
pertaining to the common heritage of mankind.
[1]
Assembly debate on 25
April 2001 (13th Sitting) (see Doc.
8901, report of the Committee on Culture, Science and Education,
rapporteur: Mr Martelli);
Doc. 9002,
opinion of the
Committee on Legal Affairs and Human Rights, rapporteur: Mr Asciak).
Text
adopted by the Assembly on 25 April 2001 (13th Sitting).
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