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ORI GIN AL ARTICLE
The Ethics of Moral Compromise for Stem CellResearch Policy
Zubin Master • G. K. D. Crozier
Published online: 12 April 2011
� Springer Science+Business Media, LLC 2011
Abstract In the US, stem cell research is at a moral impasse—many see this
research as ethically mandated due to its potential for ameliorating major diseases,
while others see this research as ethically impermissible because it typically
involves the destruction of embryos and use of ova from women. Because their
creation does not require embryos or ova, induced pluripotent stem cells offer the
most promising path for addressing the main ethical objections to stem cell
research; however, this technology is still in development. In order for scientists to
advance induced pluripotent stem cell research to a point of translational readiness,
they must continue to use ova and embryos in the interim. How then are we to
ethically move forward with stem cell research? We argue that there is personal
integrity and value in adopting a ‘moral compromise’ as a means for moving past
the moral impasse in stem cell research. In a moral compromise, each party con-
cedes part of their desired outcome in order to engage in a process that respects the
values and desires of all parties equitably. Whereas some contend that moral
compromise in stem cell research necessarily involves self-contradiction or loss of
personal integrity, we argue that in the US context, stem cell research satisfies many
of the key pre-conditions of an effective moral compromise. To illustrate our point,
we offer a model solution wherein eggs and embryos are temporarily used until non-
egg and non-embryonic sources of pluripotent stem cells are developed to a state of
translational readiness.
Z. Master (&)
Health Law Institute, Rm 462, Law Centre, University of Alberta, 89 Avenue and 111 Street,
Edmonton, AB T6G 2H5, Canada
e-mail: [email protected]
G. K. D. Crozier
Department of Philosophy, Laurentian University, 935 Ramsey Lake Road, Sudbury,
ON P3E 2C6, Canada
e-mail: [email protected]
123
Health Care Anal (2012) 20:50–65
DOI 10.1007/s10728-011-0171-2
Keywords Moral compromise � Stem cell research � Stem cell policy � Embryo �Moral status � Women’s health
AbbreviationsANT Altered nuclear transfer
hESC Human embryonic stem cell
iPSC Induced pluripotent stem cell
SCR Stem cell research
Introduction
The debates on the moral legitimacy of pluripotent stem cell research (SCR) have
focused on two central moral concerns: the moral status of human embryos and their
destruction for research, and the potential harms to women who provide ova to
create embryos for SCR. Several technological proposals have been developed that
aim to circumvent these moral issues by obtaining pluripotent stem cells without
destroying embryos or by creating pluripotent stem cells from embryo-like entities
that are (allegedly) devoid of moral status. In addition, several scientific methods
have been developed that attempt to employ ova from sources other than women for
research.
In this paper, we analyze many of these scientific proposals to derive stem cells
and conclude that most of them are not scientifically feasible and/or violate other
moral norms. Arguably, methods for inducing pluripotency of a patient’s own cells,
which do not require the use of ova from women or embryos, can address the two
central moral concerns surrounding the derivation of pluripotent stem cells.
However, current research proposals for inducing pluripotency still require the
continued use of both embryos and ova in order to bring these techniques to a state
of translational readiness.
The novel argument presented here is that a ‘moral compromise’ in SCR—in
both outcome and process—is an objective that is morally worthy and can preserve
personal integrity. A moral compromise requires all parties to acknowledge the
limitations of their values and reciprocally concede desired outcomes by accom-
modating some of the values and desires of opposing parties. We sketch a possible
moral compromise for SCR and describe how it can be applied to current US policy
and funding for SCR.
Destruction of Embryos and Harms to Women
There is richness in the diversity of views on the moral status of human embryos and
the potential physical and social harms to women ova providers. These beliefs
strongly influence the positions taken on whether ova and embryos can be used for
SCR [18]. Although some scholars have attempted to neatly link certain beliefs on
Health Care Anal (2012) 20:50–65 51
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moral status and harms to women with particular desires regarding SCR policy
choices [15, 24, 27, 55, 58, 59], there is no simple calculus for this. Nevertheless, for
the purposes of discussing a moral compromise on these two ethical issues, we
highlight the diversity of views on the moral status of human embryos and the
physical and social harms to women, and how these relate to choices on SCR policy.
The views on moral status include the position that: (a) embryos at the moment of
conception have moral status equal to persons [11]; (b) the moral status of an entity
stems from its potential for experiencing a life like ours [43]; (c) moral status is tied
to cognitive capacities such as consciousness or sentience [6, 68], the capacity to
feel joy, pain and other emotions, or the capacity to have interests and desires [23];
and (d) embryos are sacred or have symbolic weight deserving of respect [21, 55,
57, 58]. In general, those who believe embryos are sacred, persons, or perhaps
potential persons, would desire banning any SCR involving the destruction of
embryos. Those who believe that moral status requires entities to possess higher
cognitive capacities and interests, or that embryos are symbolically important,
would accept embryo destruction for SCR. Alternatively, those that believe that
embryos or embryo-like entities are symbolically monumental could also demand
the protection of embryos from destruction [47].
The policy positions accepted by individuals also considers their views on the
physical and social harms to egg donors relative to the benefits of SCR for society.
Physical risks include (a) those associated with ovarian stimulation, including
ovarian hyperstimulation syndrome, abdominal pain, fatigue, mood changes,
strokes, renal failure, heart attacks and possibly ovarian or uterine cancer and
(b) those associated with the surgical retrieval of ova such as bleeding and
hemorrhage, pelvic injury, and infection [24, 48]. The social risks to women ova
providers include exploitation and undue influence due to substantive compensation
(financial or other) [3] and gratitude for services towards physicians [34], both of
which may undermine the ability of some women to provide voluntary informed
consent. A marginalized population of women may fall victims to such exploitation,
especially in nations where the provisions on research ethics are less stringent and
where poverty is more pronounced [20, 67]. Additional concerns may arise
regarding the commodification of women’s reproductive resources that is implicit in
the provisioning of ova for SCR [69]. Furthermore, ethical issues arise in relation to
genetic privacy since immortal hESC lines derived from embryos contains the
genetic information of gamete donors [32]. Concern such as these have led many
scholars to advocate a ban on payments to egg and embryo donors for SCR.
Thus the diversity of views on moral status and the potential physical and social
harms to women create a range of policy choices for SCR including the payment
versus reasonable compensation of ova and embryo providers; the use of surplus or
excess embryos; or the creation of embryos for SCR.
Alternatives to Eggs and Embryos
Several alternative ways to derive pluripotent stem cells have been developed to
circumvent, in part, one or both of the above ethical issues by: (a) using molecular
52 Health Care Anal (2012) 20:50–65
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techniques to derive stem cells without destroying embryos; (b) manipulating ova to
prematurely halt development; and (c) using non-human animal sources of ova or
ova created from the differentiation of human embryonic stem cells (hESCs). Many
bioethics scholars have questioned whether these alternatives truly solve the above
ethical issues.
The blastocyst transfer method [41] and blastomere biopsy [10, 39] aim to use
some cells from embryos to derive pluripotent stem cells while the remainder is
transferred into women. However, the cells used to derive stem cells may
themselves be totipotent and could become a new individual (an identical twin of
the embryo) [19]. In addition, these micromanipulative techniques could impose
considerable physical damage to embryos and are unlikely to be used by parents to
create children [45]. Furthermore, they fail to recognize the potential harms to ova
providers.
A second technique called altered nuclear transfer (ANT) uses nuclear transfer
technology to create an entity with a known genetic defect that prevents normal
development [36]. Defenders of ANT claim that such entities are non-embryos and
can be used for research. It is unclear whether entities created by ANT are not
embryos in a morally significant sense despite their superficial classification and
even if they are not embryos, it doesn’t necessarily morally justify their destruction
[16, 29, 50]. Lastly, the creation of entities by ANT fails to recognize the physical
and social harms on women.
The third technique aims to use animal ova [7, 31, 52] or ova differentiated from
hESCs [46, 65] to circumvent the shortage of human eggs needed for SCR and
research cloning. There are reasons to doubt the efficacy of human-animal cybrid
research (i.e., interspecies somatic cell nuclear transfer) to resolve social justice
concerns arising from the demand for ova because stem cells derived from cybrids
may not be effective for regenerative medicine due to cross-species differences in
either gene expression [9] or energy production by the stem cells [60]. In addition,
the generation of pluripotent stem cells from cybrid embryos risks carrying cross-
species contamination and may result in moral confusion in regards to an entity that
is part human and part non-human animal [1]. Furthermore, this technique may
require the sacrifice of non-human animals in order to obtain large numbers of ova
needed for interspecies somatic cell nuclear transfer experiments which raises
significant concerns regarding animal welfare [2]. It is likely that those who support
minimizing or eliminating the use of non-human animals in research would have
good reason to question this technique. The creation of hESC-derived gametes is
only a theoretical possibility and at this time is not a substitute for using ova from
women donors as several scientific uncertainties remain [42].
In addition to the scientific and clinical effectiveness, and the ethical qualms
associated with these alternative techniques at deriving hESCs, there is also doubt in
their feasibility for clinical translation based on the costs associated with the need of
rapid and effective cell processing of large numbers of unique samples especially if
their creation involves somatic cell nuclear transfer [28, 44]. The high costs
associated with the creation of hESCs that are personalized to individuals using
somatic cell nuclear transfer technology raises questions of justice regarding who
would be able to afford such therapies [22].
Health Care Anal (2012) 20:50–65 53
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Pluripotent Stem Cells from Non-Embryonic and Non-Egg Sources
We and others have argued that the aforementioned techniques fail to resolve the
ethical challenges related to the destruction of human embryos and the potential
harms to women. We contend that to fully circumvent these two ethical issues,
pluripotent stem cells should be derived from non-embryonic and non-egg sources.
Although scientific obstacles persist, this feat could be accomplished using different
strategies to induce pluripotency of patients’ own cells.
The first method induces pluripotency of differentiated cells through fusion with
hESCs resulting in a tetraploid hybrid cell [13]. Yet scientific issues including
cytotoxicity, immunogenicity, tetraploidy, and possible tumorigenecity post-trans-
plantation remain [62] as well as moral concerns with the use of hESCs since they
are originally products of embryos.
A second theoretical scientific alternative to creating patient-specific pluripotent
cells may be to transfer the nucleus of a somatic cell into an enucleated hESC or to
inject cytoplasm from hESCs or human ova into differentiated cells. Although
nuclear transfer experiments have been performed using ova, the ovum is the largest
cell of the body making transfer technically possible. Microinjection into cells
would be technically challenging requiring the development of more sophisticated
microsurgical techniques. This technique also uses hESCs and possibly ova.
A third method to induce pluripotency that received the most attention is the
overexpression of key genes into differentiated cells [63]. Originally there were
concerns with using viral-based vectors for overexpression, since then, viral free
techniques, the addition of exogenous factors and modified culture medium have
been used to generate these induced pluripotent stem cells (iPSCs) [35, 70, 72].
There are several issues with overexpression of genes such as their integration into
key genes and if misregulated could cause abnormal cellular processes, i.e., cancer.
Upon surpassing many of the technical hurdles associated with iPSCs, it has been
suggested that personalized regenerative medicine using iPSCs is likely to be low
tech, low cost, and easy to implement in a clinical setting [33]. That is, although the
creation of iPSCs would still require the production of individualized, high quality
cell culturing, this would be less costly than the generation of individually cloned
hESCs through somatic cell nuclear transfer.
Although iPSCs have been heralded as free of moral concern [26, 51, 56], these
techniques still require further scientific investigation prior to being substitutes for
hESCs [37]. It is also noteworthy that there are different ethical concerns
associated with iPSCs, beyond the moral status of embryos and harms to women,
including the procurement of cells, clinical translation, intellectual property,
genetic privacy, informed consent and withdrawal from consent, and conflicts of
interest [61, 71]. At present, both hESCs and iPSCs should be used in order to
further understand fundamental cellular processes, the surgical/medical risks
associated with transplantation, inappropriate stem cell behaviors post-transplan-
tation, and cell procurement, processing and manufacturing strategies [38, 49].
Despite the remaining scientific and ethical questions, we advocate techniques that
do not obtain eggs from women or create embryos to derive at patient specific
stem cells.
54 Health Care Anal (2012) 20:50–65
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A Moral Compromise in SCR
Although non-egg and non-embryonic techniques seem the most ethically suitable
option to circumvent the two major ethical objections to SCR, at present, eggs and
embryos are needed for SCR to develop iPSC technology, or possibly other similar
techniques, to a state of translational readiness [37].
What are the Prospects for Agreement?
For explanatory purposes, the political positions in the US can be subdivided into
two groups: those who support continued hESC research—referred to hereafter as
‘Enthusiasts’—and those who object to hESC research on the grounds that it is
unethical (due to the embryos moral status or the potential harms to ova providers or
both)—referred to hereafter as ‘Interdictionists.’ Note that this categorization is an
abstraction, useful in the simplicity it offers for the purpose of modeling how a
moral compromise might be undertaken. In reality, the categories themselves
contain a diversity of perspectives, and some people may even identify with aspects
of both categories. Nevertheless, this categorization offers an abstraction that is both
non-arbitrary (insofar as it maps roughly onto the actual political landscape of the
US) and useful for clarifying the value of moral compromise.
It is not possible for both of these groups to have their desires regarding SCR
completely satisfied. Are we thus at an impasse? We contend that this is not the
case. In this section, we argue that the model of ‘moral compromise’ is a viable
option—indeed, it may be the most ethically sound alternative available.
Although the members of these two groups will typically diverge in the policies
they support, and are commonly conceived of as being at loggerheads, it is useful to
note that there are several points on which members of both camps will be in
agreement.1 Specifically, both Enthusiasts and Interdictionists will agree on the
following points:
1. There is value in arriving at an agreement.
All things being equal, a quick resolution to this debate would have benefits in
terms of saving public and human resources which could be dedicated to other
important projects.
2. It is the case that hESC research is morally significant.
Though some in the Enthusiast camp might argue that ethics has no role to play
in science, which should proceed unfettered by considerations of morality, this
would be an extreme view. Most would agree with the Interdictionist camp that
(a) women participants can be physically harmed while some even coerced and
(b) that human embryos at minimum are symbolic of human life and thus of moral
significance.
1 The structure of this argument is based loosely on DeGrazia’s [14] work on animal ethics.
Health Care Anal (2012) 20:50–65 55
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3. There is value in reducing the usage of embryos and ova when possible, and
alternative methods of research should be explored.
Even the staunchest Enthusiast will concur that alternative methods might have
benefits not offered by hESCs, that these alternatives might be cheaper, and that the
political support for such research would offer benefits for scientific progress
(insofar as public support for projects can be beneficial in terms of securing public
funding and making it generally easier for researchers to pursue their projects).
4. The objectives pursued by SCR are valuable goals.
Despite disagreement on whether the ends justify the means, the ends themselves
(healing the sick, advancing biological understanding, etc.) are objectives valued to
some degree by members of both camps.
5. In principle, SCR need not be morally objectionable.
This might seem like a stretch at first for those in the Interdictionist camp. But if,
however hypothetically, it could be guaranteed that pluripotent stem cells could be
procured without any harm to embryos or women in either the short or the long
term, nearly all members of the Interdictionist camp would not find this research
objectionable.
6. Some destruction of embryos can be justified, as can some procurement of ova
from women.
At first glance this point might also seem implausible, but closer reflection
reveals that this claim is not all that farfetched. Consider the first part of this claim,
regarding the destruction of embryos. In the US, most citizens—even those who
oppose the destruction of embryos for hESC research—contend that there are some
circumstances under which embryos can be destroyed: for example, when the
embryo is a product of rape or incest, when the health of the pregnant woman or
another fetus (in cases of higher order multiples) is at serious risk, for improving
assisted fertility procedures such as IVF or for providing training of technicians, or
when the embryo is of poor quality or carries a disease mutation that will severely
harm the resulting child. Similarly, consider the second part of this claim. Most
concerns regarding the procurement of ova stem from concern for the health of
women and the potential coercion they may be under from high fees or to offset the
costs of fertility treatments. If these material conditions were different such that
freedom from coercion was guaranteed and harms to women were eliminated—for
example, if medical techniques were developed so that ova providers were as safe as
those who provide semen for banks or sell their hair to wig manufacturers—there
would be no objection to the procurement of ova per se.
This final point, of course, merits further discussion. Although most members of
both camps would, on reflection, support this statement, there are some who will
not. For example, some will contend that embryo destruction is impermissible under
any of these circumstances (for example, some who strictly follow the doctrine of
the Catholic Church). However, these voices are few in the US. Although we
believe that moral minorities of this type have a valuable role to play in the creation
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of public policies regarding hESC research, we admit that for these groups a moral
compromise of the sort we propose will be incompatible with their personal
integrity, and thus unacceptable to them. This is one of the reasons that the moral
compromise proposed below is attuned to the US political climate, and might not be
appropriate for other countries.
The six points of agreement might not seem like much, but in the heated political
climate of US hESC debates it is useful to show that there is some overlap in the
beliefs and interests of parties on all sides. This does not mean, however, that there
are not important and deep points of moral disagreement that remain. Specifically,
these camps diverge on the following important points: (i) how much moral status to
ascribe to embryos; (ii) how heavily the harms to women are to be weighed; and (iii)
whether current protections for these groups are adequate. By clarifying these points
of agreement and disagreement, we are laying the groundwork for a theory of moral
compromise in SCR.
Moral Compromise
By compromise, we refer to a situation whereby two or more parties who are in
fundamental moral disagreement on a particular issue come to agree on a resolution
that ‘splits the difference’—that is, every party concedes some part of their
expectations. Although none of the parties obtains exactly what they prefer, the
overall outcome is valuable to all parties because: (a) none of the parties concede
their entire set of expectations, meaning it is not the worst possible outcome for any
of the parties; and (b) the alternative of failing to reach any agreement could result
in the worst possible outcome for at least one of the parties, and it is not clear which
one. In situations of severe moral disagreement, a compromise is not meant to end
the disagreement, but rather to find an acceptable solution for a contentious issue.
Compromises require concessions, but why should anyone concede on matters of
moral principle when they do not recognize the legitimacy of their opponent’s moral
principles? Indeed, it could be argued that such actions would be insincere or a
betrayal of one’s beliefs or values at the cost of diminished personal integrity [53].
Although many see no value in compromise solutions, others have argued that,
under the right circumstances, moral compromises can be both ethical and integrity-
preserving. As members of a society that values the participation of all citizens in
the development of rules and regulations, US citizens must engage in moral
compromise as a part of everyday life. In a modern democratic society with a
plurality of moral views, to lead a well-integrated life requires both concession and
reciprocity [5, 25]—especially in situations where there is an indeterminacy of
value-rankings on particular moral issues [66]. The preservation of integrity in a
pluralistic society requires more than ensuring consistency in one’s beliefs and
practices; it requires individuals to acknowledge both the limits of their own
moralities and the legitimacy of the competing interests of others. A moral
compromise requires persons to be open to rational persuasion and mutual trust [5,
25, 40]. While acknowledging the reasonableness of others’ views, a moral
compromise likewise requires receiving equal recognition of one’s own views,
Health Care Anal (2012) 20:50–65 57
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thereby permitting the preservation of integrity for all those who engage in mutual
concessions [40].
There is however a practical side to compromises. Theodore Benditt [4] argues
that most compromises are not over principles, but over a policy or program on a
given issue where each party has taken a position based on the principles they
believe. Policy choices are tangible items that can be bartered, traded and
compromised on. It is thus not surprising that democratic politics is the art of
compromise; politicians need to concede some things in order to obtain others. In
the context of SCR, some Interdictionists could be more concerned with harms to
women than with the moral status of human embryos and thus may be willing to
concede to using surplus embryos for research but definitely not to permitting
payments. Thus different individuals and groups can concede certain desires while
receiving some of their interests that are more closely aligned to their beliefs.
Moreover, compromises are not meant to explain the rightness or wrongness of
different positions; their value derives from settling disagreements on policy choices
in a peaceful manner, through reciprocity and respect, so as to advance towards
social goals. In this sense, a moral compromise is not indicative of compromising on
deep moral beliefs, but engaging in a process of reciprocal appreciation and
understanding of different positions in a liberal democracy and attempting to resolve
the issue to reach mutually satisfactory interests.
Conditions for Moral Compromise in SCR
Benjamin [5] outlines five criteria for determining when a moral compromise is
appropriate. While there is no algorithm for determining in which cases a moral
compromise is acceptable, these criteria suggest some of the conditions which are
conducive to selecting moral compromises. Although individually none is
necessary, and jointly they may not be sufficient, the following criteria outline
common preconditions for an effective moral compromise: (a) factual uncertainty,
(b) moral complexity, (c) the need for a relatively immediate decision or action,
(d) the desire to maintain a continuing cooperative relationship, and (e) a scarcity of
resources.
The case could be made that all five of Benjamin’s conditions apply, to some
degree, to SCR. However, the first three are the most salient. First, there is factualuncertainty regarding the potential benefits of various forms of SCR: for example,
the feasibility and time-frame required for the development of clinical applications
from hESCs, or techniques for inducing pluripotency as substitutes for hESCs.
Second, the SCR debate is morally complex, involving multiple layers of deep
disagreements regarding what is the moral status of various types of embryos, what
measures would be appropriate for protecting women ova providers, and what
weight should be given to the chance that SCR may benefit individuals in the future.
Many of the diverse and conflicting positions voiced are supported by morally
worthy considerations, even if these positions are not universally accepted. Finally,
there is a need for immediate decisive action since suspending decision making
would be tantamount to supporting one position over another. Since several of
Benjamin’s criteria are present in the case of SCR, there is good reason to think that
58 Health Care Anal (2012) 20:50–65
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the moral disagreements regarding SCR are amenable to moral compromise. In the
following section, we outline how such a moral compromise can proceed.
A Model of Moral Compromise in SCR
Many scholars have expounded upon the difficulties in preserving personal integrity
on a belief of moral status and the use of surplus embryos for research concluding
that such compromises are a betrayal of values and principles [15, 17, 64]. Our
proposal is that a compromise on conducting SCR can satisfy the majority of
interested parties through a process involving two procedures. Note that our purpose
here is not to propose a specific policy or set of policies, but rather to propose one
possible outcome of a moral compromise in SCR that could serve as a model in the
real world. Interested groups and individuals would deliberate and outline the actual
conditions of a compromise in order for the policy framework to have any real
political traction.
A compromise can satisfy Enthusiasts and Interdictionists equitably by equally
respecting the values and desires of both parties. We propose the following two-
phase procedure as one possible way for these two polar positions on SCR to reach a
moral compromise (outlined in Table 1). Broadly speaking, our proposal is that the
use of eggs and embryos would be permitted in the initial phase of the procedure
and prohibited in the subsequent phase. Notably, the shift from the first to the
second phase is initiated once a reliable and plentiful source of stem cells can be
secured without the destruction of embryos or the procurement of ova from women.
The first procedure terminates after an agreed upon time has passed. At this time,
either the goals of a non-oocyte and non-embryo source of pluripotent stem cells
will be achieved, or it will not. If it has, then the second phase begins. If, however, it
has not, a moratorium will be placed on research that involves destroying embryos
and procuring ova, and the parties must return to deliberations on how to proceed in
the future.
Although this may appear to be a procedure that heavily favors the interests of
Enthusiasts because they would be satisfied by the circumstances outlined in both
phases, more detail reveals how the interests of Interdictionists are also respected.
Specifically, several concessions are made by Enthusiasts throughout the first phase
which include: (1) limiting the use of embryos to surplus and non-viable embryos;
(2) prohibiting substantive payments to ova donors (though allowing for reasonable
compensation); (3) developing and following a concrete plan for the efficient use
and distribution of embryos; and (4) concentrating research funds on projects with
the best chance of furthering the laudable goal of deriving stem cells from non-
embryo sources and without using ova from women. These last two points are
explained below.
After the time limit on the initial phase has expired, the degree to which these
concessions are satisfied will be influential in determining what will occur
subsequently. To the extent that progress has been made in reducing, rather than
increasing, social dependency on oocytes and embryos, Interdictionists might be
more amenable to repeating the conditions of the first phase of the moral
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compromise. Below we further describe how our example of moral compromise can
be used to develop SCR policy and influence funding priorities.
Application of a Moral Compromise in SCR Policy and Funding
A compromise can be applied in SCR policy and funding in order to achieve the
desires and concessions discussed above in our model compromise. Several policy
and funding tools will need to be implemented. Initially, this would require
repealing the Dickey-Wicker Amendment (a rider on the appropriations bill
renewed annually) [12] and the development of policies on the conduct of embryo
research, reimbursements to donors, and other aspects of donation (such as consent).
The time periods for the two phases can be applied in policy through the use of
sunset provisions.
Table 1 The benefits and concessions in an example of moral compromise on SCR
Category Benefits Concessions
Phase 1: Eggs and embryo use is permitted with restrictions
Enthusiasts Continued progress in SCR using ova
and embryos
Use of embryos limited to surplus
and non-viable embryos
Use of ova limited due to a lack of
offering substantive payments, but
reimbursements are permitted
Efficient use and sharing of human
biological resources
Emphasize SCR designed to reduce
use of ova and embryos
Interdictionists No payments to ova providers
Limitations in use of embryos
Concrete steps taken towards
reducing social dependency on ova
and embryos
Temporary use of embryos in
research
Temporary use of ova in research
Phase 2: Eggs and embryos are not permitted or their use is substantially limited
Enthusiasts Continued progress in SCR Have to use non-embryo methods
for SCR
Have to use non-ova methods
for SCR
Interdictionists No embryos destroyed for SCR
No ova procured for SCR
The model compromise sketched in this essay uses two phases to satisfy both Enthusiasts and Inter-
dictionists. In the first phase, Enthusiasts receive benefits of continued progress in SCR while making
several concessions on the type of embryos used, payments to ova donors, the efficient sharing of
biological resources, and emphasizing research using non-ova and non-embryo techniques to derive stem
cells. Interdictionists on the other hand receive the benefits of ova providers not being solicited or coerced
through payments, that embryos used for SCR are limited, and that steps are being taken to reduce the
social dependency of ova and embryos for SCR. Interdictionists concede that some ova and embryos are
still being used for SCR. In phase 2, Enthusiasts benefit from continued SCR using methods that do not
use ova or embryos while Interdictionists benefit by not having ova and embryos being used for SCR
60 Health Care Anal (2012) 20:50–65
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Along with permitting publically funded SCR in a regulated and time-dependent
manner, policy focusing on the efficient use of embryos should also be developed in
order to balance concessions between Enthusiasts and Interdictionists. For some
Interdictionists, every embryo lost may be considered a loss of a human life and so
embryos should be used to their fullest potential [32] based on the principle of
efficiency.2 To maximize the use of limited embryonic material in the initial phase,
we propose that excess embryos created for any purpose (e.g., assisted reproduction,
training, or research) should be used to subsequently derive pluripotent stem cells
after having satisfied the original purpose for which they were created.3 This will
require great efforts to communicate and coordinate with researchers and assisted
reproductive clinics to not destroy embryos after they have been used for the initial
purpose. A national system for coordinating the efficient sharing of embryos could
go a long way towards reducing the generation (and destruction) of more embryos
than what might be considered necessary. Such a system could involve providing
powers to a governing body to oversee the execution of the compromise.
As part of a commitment to the efficient use of embryos—an important part of
preserving fairness in the concessions between Enthusiasts and Interdictionists—
research should focus efforts on pursuing the development of ovum- and embryo-
free techniques. This research will require coordinated efforts with funding focused
in key areas of SCR (e.g., iPSC technology) by the major state and federal funding
organizations—including the National Institutes of Health and the National Science
Foundation.
Our paper has both a political and philosophical dimension. Not all political
compromises involve moral compromises, and vice versa; however, in the case of
stem cell policy these seem inseparable. In the context of SCR, the policies a person
advocates are determined by their moral position; and the various parties cannot
achieve a common policy decision without some flexibility regarding the objectives
that they believe to be warranted by their diverse moral positions. Thus, in terms of
politics, we are proposing policies that the different sides could agree to; however,
we are not proposing that our specific model of moral compromise is one that ought
to be implemented. Because of the deep moral convictions in the embryo and SCR
debate, the concessions made take on a distributive approach for compromise where
the concessions are minimized and the overall outcome is only slightly more
satisfactory to both sides [8].
The political significance of this paper is abundantly clear in the popular
messages of the US’s Tea Party movement, which vociferously opposes policies
that ‘split the difference’ between liberal and conservative positions on the basis
2 Resnik [54] outlines several principles in the ethics of science one of which is that scientists should use
limited resources efficiently which includes economic, human, and technological resources.3 Embryos can be created for reproductive purposes, for research towards improving assisted
reproductive technologies, to train technicians, and to test materials for toxicity. For example, when
testing a new culture medium against a gold standard, gametes are placed in the two different media and
their potential to fertilize and develop is evaluated. After embryos are scored, they are typically discarded
since they cannot be used for reproductive purposes. Our suggestion is that these surplus embryos, which
were once created for different credible intents, should be used to derive pluripotent stem cells instead of
being discarded.
Health Care Anal (2012) 20:50–65 61
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that this represents a loss of personal integrity—a compromised morality, rather
than a moral compromise. In practical application, the specific policy problem in the
US is not compromise in a general sense but whether such a compromise can be
applied to federal public service funding, since state or private funding is allowed.
This problem entails questions of political philosophy about the use of public funds
for activities about which there is deep moral disagreement. Such questions are
beyond the scope of this paper.
The main philosophical targets of the paper are those who, like Devolder and
Harris, have rejected compromised positions (such as the use of surplus embryos) on
the claim that such positions are based upon inconsistent values and positions. We
have argued, to the contrary, that there can be great personal integrity in adopting a
moral compromise in SCR. To this extent, our paper is an exercise in the theory of
moral compromise, by applying it to moral argumentation on SCR.
Although we have presented an example of a moral compromise in SCR, we
recognize that for democratically legitimate and justified decisions to be translated
into policy, citizens must first engage in deliberation to reach a moral agreement on
contentious issues by providing reasons that can be accepted by those who are
affected by the action [30]. As reciprocity is a fundamental tenet in moral
deliberation, we imagine a policy consultation process where concerned parties
have the opportunity to extensively deliberate on the conditions of the moral
compromise and reason reciprocally while recognizing and respecting the moral
worth of opposing views. Thus, deliberation will probably be a key component in
the consultation process for achieving a moral compromise in SCR.
Conclusion
We have argued that a moral compromise offers the promise of an optimally ethical
outcome in contemporary US debates regarding the ethics of SCR. In moral
compromise, each party concedes part of their desired outcome in order to engage in
a process that respects the values of all parties equitably. We have outlined an
example of one set of possible conditions to provide moral compromise in SCR and
have applied it to US policy and scientific funding. Although the particular proposal
presented here would not fully satisfy the desires of either SCR Enthusiasts or
Interdictionists, it does offer several distinct and compelling advantages to both
parties. First, there is value in achieving the benefits of SCR for society and to
develop techniques that reduce or eliminate other moral harms, including the
creation of embryos for destruction and the procurement of ova from women.
Second, there is benevolence when citizens participate in a democratic process of
policy-making for the overall good in society. Lastly, there is virtue when citizens
engage in debate, but not with the intent of convincing the opposition of the
rightness of one’s principles and policy choices, but to facilitate a reciprocal
understanding and appreciation for opposing views and in attempting to accom-
modate the desires of the opposition [30]. Bioethicists concerned with the morality
of SCR need to further consider the value of a moral compromise as a practical and
reasonable solution to address the diverse moral perspectives in SCR.
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Acknowledgments We would like to thank Dr. Francoise Baylis and the Novel Tech Ethics research
team, Dr. David B. Resnik, Dr. Andrew Fenton, and Ms. Sasha Kontic for valuable feedback. We are also
grateful to the anonymous reviewers of the manuscript for thoughtful feedback. This work was supported
in part by a grant from the Stem Cell Network. ZM was affiliated with the Sprott Centre for Stem Cell
Research and the Ottawa Hospital Research Institute, University of Ottawa when initially writing this
manuscript. GKD Crozier was affiliated with the Department of Philosophy, Loyola University Chicago
when first drafting the manuscript. The views expressed here are those of the authors and do not reflect the
positions of their academic institutions, Health Canada, or the Government of Canada.
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