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Final Report (all chapters)

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progress over time may provide new means, they will not undermine the corresponding<br />

prohibitions. Second, the prohibitions are worded in such a way as to ensure that reproductive<br />

technologies are used exclusively for reproductive purposes narrowly defined, though as we<br />

show below, the intent to reproduce does not justify the use of each and every reproductive<br />

technology.<br />

The centerpiece of these prohibitions is Section 5. Section 5(1)(a) bans any kind of cloning,<br />

including research cloning, but does so not by specific<strong>all</strong>y prohibiting somatic cell nuclear<br />

transfer. Rather, it defines cloning in functional terms. Thus, this section simply proscribes the<br />

creation of “a human clone, by using any technique.” Consistent with its focus on human<br />

reproduction, Section 5 bans the creation of embryos for any purpose other then procreation,<br />

medical training, or the improvement of reproductive technologies. 44<br />

Medical and clinical<br />

research on human embryos remains legal, though it may be difficult, as a matter of practice, to<br />

determine whether a research protocol involving human embryos is indeed designed to improve<br />

the safety and efficacy of existing reproductive technologies. This distinction becomes<br />

particularly problematic when research protocols are designed to explore questions impinging<br />

only indirectly on actual medical practice. 45<br />

Reproductive intent alone does not justify resorting to any and every reproductive<br />

technology. Accordingly, Section 5 prohibits several reproductive procedures. For example, it<br />

bans any technique that could lead to the creation of embryos from fetuses or from embryonic<br />

stem cells. 46 This prohibition is a direct response to the announcement made in 2003 by an Israeli<br />

research group that it had successfully retrieved viable oocytes from aborted fetuses, and to other<br />

experiments in mice showing that it may be possible to derive sperm-like cells and oocytes from<br />

stem cells (see chapter 4 for details). In keeping with a narrow understanding of reproduction,<br />

Section 5 also proscribes the use of sex-selection technologies except for preventing sex-linked<br />

diseases. 47 As with other prohibitions discussed in this section, this ban does not refer to a<br />

specific sex-selection technology; it simply proscribes the use of any and <strong>all</strong> technological means<br />

for elective sex selection. Also proscribed are <strong>all</strong> forms of genetic engineering that would<br />

produce an inheritable genetic modification. 48 Presumably this prohibition extends to ooplasm<br />

transfer, as this procedure indeed produces an inheritable genetic modification by passing on<br />

mitochondrial DNA from a third party. Furthermore, innovative reproductive approaches that<br />

involve the use of animal tissues, such as co-culture, are also prohibited. 49 In keeping with<br />

44<br />

45<br />

46<br />

47<br />

48<br />

49<br />

See Section 5(1)(b).<br />

The AHRA does not ban stem cell research, however. Section 5(1)(b) only bans the creation of in vitro embryos<br />

for any purpose other than human reproduction. The act does not explicitly require the transfer of <strong>all</strong> in vitro<br />

embryos into a woman’s uterus. This introduces the possibility that existing, cryopreserved embryos can be<br />

donated for research, a solution that is reminiscent of the Australian approach to legalizing stem cell research.<br />

See Section 5(1)(c).<br />

See Section 5(1)(e).<br />

See Section 5(1)(f).<br />

See Section 5(1)(h).<br />

163

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