Republic of the Philippines
College of Engineering and Architecture
Electrical Engineering Department
“Medical Evolution: Breaking Boundaries in Human Cloning”
Researchers:
Adrian R. Motea
Jhae Art S. De Jesus
Louie T. Reasonda
Lemmuel A. Allado
Von Khirby J. Eupalao
Instructor:
Mr. Krystian Carvajal
Hypothesis
The successful implementation of human cloning in 2050
revolutionized medicine, providing solutions to organ shortages,
personalized therapies, and advances in regenerative medicine
Introduction
Human life is priceless and has a worth that exceeds all standards.
However, the scarcity of viable organs for transplant is a clear and tragic
reality that results in an unbelievable amount of deaths. The scarcity of
suitable organs for transplant continues to be a serious concern in the
medical field, forcing people to remain on waiting lists and desire for a
chance to regain their health and energy.
According to Welle (2019), India has one of the lowest rates of organ
donation in the world, trailing well behind the rest of the world. Experts feel
that considerable improvements are required to increase the South Asian
nation's donor rate. Other countries are experiencing organ shortages as well.
Based to the PMC or Pubmed Central (2019), New York had the lowest
organ donor registration rate (22.7%) while Oregon had the highest (56.7%).
The 2019 data from the International Registry in Organ Donation and
Transplantation (IRODAT) states that the United States alone, a staggering
number of more than 100,000 people are persistently waiting for an organ
transplant, a figure reflected in tens of thousands around the world. the rate
of organ donation in European countries such as Spain was 49.9 patients per
million population (ppmp) while the Philippines only had a rate of 0.087
ppmp. Every day that a suitable donor organ isn’t accessible signifies a race
against time, a fight for survival, and, unfortunately, the loss of a life. This
scarcity highlights the critical need for new ways to bridge the gap between
organ supply and demand, bring hope where despair lurks, and recognize the
dignity of every life waiting for a second shot at life through transplantation.
Meanwhile, In the area of medical advances, creating cloned humans
or human organs captures our imagination and sheds speculative light on the
field of medicine. The year 2050, the field of human cloning is emerging as
a fascinating field waiting for technology to revolutionize medicine. This
case study embarks on a visionary journey and explores the potential of
cloned humans as a beacon of hope in the field of medicine. Human cloning
refers to the scientific process of creating an identical genetic copy of a
human organs or human being.
The concept of human cloning has been a topic of interest and debate
for many years. The origins of human cloning can be traced back to the
scientific breakthroughs and advancements in reproductive technologies.
According to Gunn (2021) the roots of cloning began in the nineteenth
century. In 1885, German biologist Hans Driesch showed that blastomeres of
two-cell sea urchin embryos could be physically separated and two entire
embryos formed from each blastomere. This was the first-ever
demonstration of artificial embryo twinning, the process of separating
embryonic cells in the early stages of development. Each separated cell
continues to grow and can be implanted into a surrogate. In agreement with
Shannon Gunn, George Vaniotis (2021) stated that scientists first began
studying the process of artificial cloning at the turn of the last century, when
a German scientist, Hans Adolf Eduard Driesch, began researching
reproduction in salamanders. In 1902, he created a set of twin salamanders
by dividing an embryo into two separate, viable embryos.
Runetta et al. (2019) stated in their article that reproductive
cloning was originally carried out by artificial “twinning,” or embryo
splitting, which was first performed on a salamander embryo in the early
1900s by German embryologist Hans Spemann. Later, Spemann, developed
another cloning procedure known as nuclear transfer. This procedure was
performed in 1952 by American scientists Robert W. Briggs and Thomas J.
King who used DNA from embryonic cells of the frog Rana pipiens to
generate cloned tadpoles. In 1958 British biologist John Bertrand Gurdon
successfully carried out nuclear transfer using DNA from adult intestinal
cells of African clawed frogs.
Alberio and Wolf (2021) concluded that the birth of "Dolly the sheep"
in 1996 marked a groundbreaking achievement, challenging the long-held
belief in irreversible cellular differentiation. Dolly was significant in that she
was the first mammal cloned from an adult cell. Her birth demonstrated that
specialized cells might be employed to produce an exact recreation of the
animal from which they originated. This discovery altered scientists’
perceptions of what was possible and opened up new avenues of research in
biology and medicine, including the production of personalized stem cells
known as iPS cells. Soon after the generation of Dolly, a number of other
animals were cloned including pigs, goats, rats, mice, dogs, horses, and
mules.
Moreover, the milestones achieved by Wolf and Mitalipov,
particularly In creating a monkey from cell nuclei, highlight the possibility
of cloning genetic abnormalities in other animals for large-scale studies,
leading to better solutions and treatments. This advance enables the creation
of patient-specific genetic diseases in animal models and simplifies the
testing of drug effectiveness and side effects. Transferring the nucleus from a
human skin biopsy to mice or monkeys creates an egg with patient-specific
disease expression, enabling clinical studies in animal models and ultimately
leading to more effective medical approaches.
December 27, 2002, a group of scientist announced that the first
cloned baby had been born the day before. The girl, named Eve by the
cloning team, was said to have been born by Caesarean section at 1155 EST.
The birth at an undisclosed location went “very well”, said Brigitte
Boisselier, president of Clonaid. The company was formed in 1997. By
2004, Clonaid claimed to have successfully brought to life 14 human clones.
These claims are widely disbelieved, in part because Clonaid did not allow
independent testing of the babies, supposedly to protect the privacy of the
babies and their families. Other scientist succeeded in using the Dolly
process, technically called somatic cell nuclear transfer, to clone humans.
There are two primary methods of cloning humans: reproductive
cloning and therapeutic cloning. Reproductive cloning aims to create a
cloned human for the purpose of producing a fully developed individual. On
the other hand, therapeutic cloning focuses on creating cloned cells or
tissues for medical purposes, such as generating organs for transplantation or
studying specific diseases.
Yu (2022) claimed that the potential of therapeutic cloning to repair
organs in the body is extremely promising, particularly to alleviate the
severe shortage of organs available for transplantation. The integration of
therapeutic cloning represents a ray of hope and offers a possible solution to
shorten the long and arduous treatment times that patients often face. The
alarming statistic of more than 20 deaths waiting for organ donations every
day highlights the urgency of innovative interventions. Kidney waiting
times, which can last up to five years or even longer in certain cases, place a
significant burden on patients looking for suitable partners. The widespread
availability of therapeutic cloning could revolutionize organ transplantation,
eliminating these long waits and offering a glimmer of hope to countless
people in desperate need. The controlled environment enabled by therapeutic
cloning represents a viable option for creating critical organs, effectively
eliminating waiting times and potentially saving significant long-term
healthcare costs. Furthermore, the identical DNA match between the cloned
organ and the recipient prevents the possibility of organ rejection after
transplantation, thus providing a definitive solution to this ongoing problem.
Therapeutic cloning represents a transformative prospect in which
dependence on donor organs could become obsolete. The prevailing medical
paradigm requires the death of one person so that another person can benefit
from a life-saving heart transplant. This reliance on deceased donors and the
need for a precise match between donor and recipient pose significant
challenges in obtaining organs for transplantation and make them extremely
scarce. The need for viable organs at the time of a donor’s death, coupled
with strict compatibility criteria, exacerbates the shortage and complexity of
organ procurement. However, the advent of therapeutic cloning offers an
innovative alternative that may make reliance on donor organs unnecessary.
This innovative approach to organ recovery avoids reliance on deceased
donors, provides a prospective solution to the critical shortage of organs for
transplantation, and avoids the need for an exact match between donor and
recipient. The ability to grow and maintain organs through therapeutic
cloning could revolutionize the organ transplant landscape, enabling a
sustainable and affordable supply of organs without having to wait for a
tragic loss of life.
However, the ethical and social considerations surrounding these
advances cannot be ignored. This narrative addresses the complex web of
ethical dilemmas, carefully balancing the benefits with the moral
implications. It envisions a future in which cloned human tissues are
seamlessly integrated into healthcare systems while reflecting public
acceptance. At the heart of this narrative is the prospect of personalized
medical therapies, in which cloned human cells pave the way for treatments
tailored to individual genetic profiles. This innovative paradigm ensures that
precision medicine reaches new heights. As we embark on this visionary
odyssey through medical innovation, ethical considerations, and social
introspection, let us outline the hypothetical creation of cloned humans in
2050.
Cloning applies the idea of gene alteration, which is significant in the
improvement of productivity and health of livestock and crops, this ensures
that the plants and animals are even more adaptable to the new environment
and therefore have more survival skills and adaptability; this means that the
humans are protecting God’s creations from extinction through this
technology. For humans to protect and take care of God’s creations they
need to, first of all, take care of themselves, they need to survive in the
future, they need to be healthy and strong, they need to live as long as
possible. Cloning will offer them these opportunities.
What moral right might protect at least some access to the use of
human cloning? Some commentators have argued that a commitment to
individual liberty, as defended by J. S. Mill (2016), requires that individuals
be left free to use human cloning if they so choose and if their doing so does
not cause significant harms to others, but liberty is too broad in scope to be
an uncontroversial moral right . Human cloning is a means of reproduction
(in the most literal sense), and so the most plausible moral right at stake in
its use is a right to reproductive freedom or procreative liberty. Reproductive
freedom includes not only the familiar right to choose not to reproduce, for
example by means of contraception or abortion, but also the right to
reproduce.
Moreover, There is a different moral right which might be thought to
be at stake in the dispute about human cloning—the right to freedom of
scientific inquiry and research in the acquisition of knowledge. If there is
such a right, it would presumably be violated by a legal prohibition of
research on human cloning, although the government could still permissibly
decide not to spend public funds to support such research. Leaving aside for
the moment human subject ethical concerns, research on human cloning
might provide valuable scientific medical knowledge beyond simply
knowledge about how to carry out human cloning. Whether or not there is a
moral right to freedom of scientific inquiry—for example, as part of a right
to free expression—prohibiting and stopping scientific research and inquiry
is a serious matter and precedent which should only be undertaken when
necessary to prevent grave violations of human rights or to protect
fundamental interests. But even for opponents of human cloning, the
fundamental moral issue is not acquiring the knowledge that would make it
possible, but using that knowledge to do human cloning. Since it is possible
to prohibit human cloning itself, without prohibiting all research on it, it is
not necessary to limit the freedom of scientific inquiry in order to prevent
human cloning from taking place. But this means as well that a right to
freedom of scientific inquiry could only protect research on human cloning,
not its use. For this reason, I believe the fundamental moral right which
provides presumptive moral support for permitting the use of human cloning
is the right to reproductive freedom, not the right to freedom of scientific
inquiry.
In addition, The extraction of embryonic stem cells, integral to
therapeutic cloning, remains a contentious issue for many. Ethical concerns
persist irrespective of whether these cells are intended to alleviate the
suffering of individuals afflicted by ailments. The utilization of this
technology raises ethical red flags for some, underscoring the moral
quandaries associated with manipulating human embryos. Moreover, the
relatively simplified process of cloning humans using female egg cells alone
poses a complex ethical dilemma. The unrestricted capacity for reproduction
through cloning, relying solely on female egg cells, potentially undermines
the importance of male procreation in human reproduction. This aspect
could significantly influence societal norms regarding family ethics and
traditions. The transformative potential of therapeutic cloning is
overshadowed by the ethical complexities it introduces, sparking debates
surrounding the morality of manipulating human embryos and reshaping the
fundamental fabric of traditional family ethics. This imagined world has the
potential to reshape healthcare and usher in a new era of medical
possibilities. It is important to note that human cloning raises various ethical,
moral, and legal concerns. Cloning technology is still in the experimental
stage and has not been successfully implemented for reproducing a full-term
human clone. Many countries have banned or put restrictions on human
cloning due to these ethical considerations.
Assumption
In the envisioned scenario of 2050, the realm of human cloning has
experienced unprecedented progress, reshaping the dynamics of organ
transplantation. The advent of organ cloning emerges as a groundbreaking
solution, significantly altering the trajectory of healthcare outcomes.
The ethical pros and cons of human cloning, as we see them at this
time, are sufficiently balanced and uncertain that there is not an ethically
decisive case either for or against permitting it or doing it. Contrary to the
pronouncements of many of its opponents, human cloning seems not to be a
violation of moral or human rights. But it does risk some significant
individual or social harms, although most are based on common public
confusions about genetic determinism, human identity, and the effects of
human cloning. Because most moral reasons against doing human cloning
remain speculative, they seem insufficient to warrant at this time a complete
legal prohibition of either research on or use of human cloning.
The transformative impact of human cloning extends beyond mere
survival, it introduces shifts in healthcare accessibility. Previously
insurmountable barriers, such as the prohibitive costs of organ procurement
or the extended durations spent on waiting lists, have been dismantled .
Human cloning stands as a pivotal force In this evolution, offering the
capability to develop tissues and organs that harmonize seamlessly with
patients’ immune systems. This breakthrough eliminates the hurdles of
exorbitant costs and lengthy waitlists, ushering in a new era of healthcare
accessibility.
References
Alberio, R., & Wolf, E. (2021). Nuclear transfer and the development of
genetically modified/gene edited livestock. Retrieved December 1, 2023
from,. https://doi.org/10.1530/rep-21-0078
Abouna, G. M. (2008). Organ shortage crisis: problems and possible solutions.
Retrieved November 28, 2023 from, Proceedings, 40(1), 34–
38. https://doi.org/10.1016/j.transproceed.2007.11.067
Cooper et al. (2014). Progress in pig-to-non-human primate transplantation
models: a comprehensive review of the
literature. Xenotransplantation 21 397–419. Retrieved December 1, 2023
from, (https://doi.org/10.1111/xen.12127)
De Jesus et al. (2023). Attitude and Perception Among Emergency Department
Healthcare Workers on Organ Donation: A Multicenter Before and After
Study. Retrieved November 26, 2023 from,
https://www.jmust.org/elib/journal/doi/10.35460/2546-1621.2023-0039/
full#:~:text=As%20per%20the%202019%20data,a%20rate%20of
%200.087%20ppmp
Dakks (2002). First ever clone baby born. Retrieved December 1, 2023 from,
https://www.cbsnews.com/news/eve-first-human-clone/
Fiske et al. (2013). Therapeutic Cloning of Embryonic Stem Cells Is Achieved.
Retrieved November 30, 2023 from,
https://www.michaeljfox.org/news/therapeutic-cloning-embryonic-stem-
cells-achieved
Gunn (2021). Evolution of cloning: A good Dolly show . Retrieved December 3,
2023 from, https://frontlinegenomics.com/evolution-of-cloning-a-dolly-
good-show/#:~:text=The%20roots%20of%20cloning%20began,embryos
%20formed%20from%20each%20blastomere
Greely (2020). Human reproductive cloning: The curious incident of the dog in the
night-time .Retrieved November 29, 2023 from,
https://www.statnews.com/2020/02/21/human-reproductive-cloning-curious-
incident-of-the-dog-in-the-night-time/#:~:text=Undaunted%2C%20Clonaid
%20moved%20its%20operations,to%20life%2014%20human%20clones
Huang H. (2014). Knowledge, attitudes, and willingness toward organ donation
among health professionals. Retrieved December 3, 2023 from,
https://journals.lww.com/transplantjournal/fulltext/2015/07000/knowledge,_
attitudes,_and_willingness_toward_organ.17.aspx
Kehan Yu (Kingston). (2022). Therapeutic Cloning: its applications, advantages,
and disadvantages. Retrieved November 28, 2023, from
https://clausiuspress.com/conferences/LNMLS/BLSME%202022/Y0844.pdf
Med (2017). Therapeutic cloning: promises and issues. Retrieved November 27,
2023 from, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323472/
Shafique, S. (2023). Human cloning: recent advances and bioethical issues. In
Springer eBooks (pp. 177–192). Retrieved November 29, 2023 from,
https://doi.org/10.1007/978-3-031-29451-8_11
Wadhwani et al. (2021). Neighborhood socioeconomic deprivation, racial
segregation, and organ donation across 5 states Retrieved November 26,
2023 from,
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191504/#:~:text=Ne
w%20York%20had%20the%20lowest,Oregon%20the%20highest
%20(56.7%25)