We are now entering the era of gene-editing where the power to design life is almost within our hands. But should we do it?
By: Sean Lemuel L. Santos (Hybrizyme)
In 2018, a
Chinese researcher named Dr. He Jiankiu announced that he has created the world’s
first gene-edited babies. Dr. He claims that he made these babies resistant to
HIV by editing a gene using a new, powerful molecular tool known as CRISPR. He edited
the gene known as CCR5 so that the
virus could not, supposedly, attack the immune system’s cells of the babies.
Incredible
as it may sound, Dr. He’s experiment has sparked huge safety concerns among
scientists and raised ethical issues on gene-editing.
But what
exactly is CRISPR and why is using it such a big deal?
What CRISPR was
CRISPR is a
revolutionary, gene-editing technology that was first discovered as an ancient
immune system of bacteria against invading viruses. It has two components: the CRISPR
or Clustered Regularly Interspaced Short Palindromic Repeats which are the
repeating parts in the bacteria’s DNA, and the Cas9 or CRISPR-associated protein
9 which acts like a sniper looking for any virus DNA that it could “kill”.
When a
virus infects bacteria and injects its DNA, Cas9 would cut a piece of this virus’ DNA and paste it within the CRISPR so that the bacteria could “remember” the
virus. The bacteria would then produce a copy of this virus DNA known as the
short-guide RNA (sgRNA) which Cas9 would bring as it scouts the cell for any
signs of the virus DNA. When a virus infects again, Cas9 would use the sgRNA to
look for any match. And when it does, it would chop up the virus DNA like a
paper shredder.
What CRISPR is
Now,
scientists have been able to turn CRISPR from being a shield against viruses to
being a weapon against diseases. CRISPR is now being used as a gene-editing
tool that could look for harmful genes and remove them out of the DNA. But how?
by designing the sgRNA to look exactly like a bad gene, scientists can deploy CRISPR to locate this bad gene, remove it from the DNA of an organism, and then
allow the cell to repair any resulting damage.
The
potentials of CRISPR in biology, agriculture and medicine are enormous. For one,
it can be used to genetically edit mosquitoes so that they would not carry malaria
or dengue and thereby stop the spread of these deadly diseases. It can also be
use to design crops that are resistant to drought, heat or harmful pests. More importantly,
CRISPR can be utilized to treat genetic diseases that afflict mankind such as
sickle-cell anemia, cystic fibrosis or Tay-Sachs disease.
But can CRISPR be used to design life?
But can CRISPR be used to design life?
Enter
the World of Designer Babies
In the
past, designing life is all left to chance. Parents do not have any idea if their
babies have genetic diseases until they are born and have grown up. But advancements
in medicine have changed all this. Now, parents can determine which embryos are
genetically healthy and which ones are not. They could then select the “best”
embryo to be implanted into the mother’s womb. This is done through a process known
as pre-implantation genetic diagnosis (PGD).
With CRISPR
being developed as a gene-editing tool, it could one day be used to produce babies
without genetic diseases or even babies with enhanced traits such as intelligence,
athletic ability, or creativity.
CRISPR is
cheap, powerful and limitless. It is
only a matter of time before it can be used to create designer babies. The
question then is not how it can be used to design life, but should we actually
use it for such?
Here are some things that we have to consider:
Here are some things that we have to consider:
Somatic vs. Germline Editing
There are
two types of editing that can be done using CRISPR: somatic gene editing and
germline editing. In somatic gene editing, changes in the DNA are done in any
of the individual’s cells except the sperm or the egg. As a result, any changes
(and problems) made stays within the individual and are not passed on to the
next generation.
Ethical concerns
arise mostly in germline editing where changes are made in the DNA of sperms,
eggs or human embryos. These changes are permanent and are handed down to
offspring. The problem with germline editing is that there is no informed
consent given to the future generations. It could also stir the course of human
evolution in ways we do not intend to. We might for example prefer to have all
babies HIV-resistant but if an outbreak of West Nile virus (in which
HIV-resistant people are prone to) occurs, all these babies would least likely
to survive.
Treatment vs. Enhancement
Another
concern in CRISPR is whether we should use it only to cure diseases or also utilize
it to attain genetic advantages. CRISPR can be a powerful medical tool that
could treat human diseases and thereby alleviate the suffering of millions. If
proven safe and reliable, then it should definitely be used to cure diseases.
However, the concern appears when CRISPR is to be used as a form of enhancement.
Many bioethicists are concerned that using CRISPR to improve, say intelligence
or height, could lead to a new form of eugenics wherein individuals with less of
a physical feature are deemed inferior and useless.
Affordable vs. Expensive
As what
happens to the fate of many technologies, CRISPR could also be possessed by the
hands of a few. For now, CRISPR remains affordable for research. But in the
future, only the rich might have an
easy access to this technology which tremendously widens the gap between the
rich and the poor. This could create a society whose hierarchy is based on the
quality of their genetics. Already, rich people have an environmental advantage
over poor people. They have better access to clean water, healthcare and
education. If CRISPR becomes a luxury, only the rich could have a genetic
advantage which ultimately worsens the conditions of the poor and leads to further
inequality.
Safe vs. Risky
CRISPR has already
undergone a tremendous number of experiments by a myriad of scientists for over
many years. However, there is still much that we don’t know about them. One thing
is its safety. Just recently, in a paper published in Nature, CRISPR has been found to have caused large scale deletions
and rearrangements in the DNA of mouse stem cells. As of this moment, we still
don’t know if CRISPR can accurately make the edit we intend to. And even if it
can, we are also unsure if it is not changing the normal genes we don’t want to
be edited. These so-called off-target effects in the DNA can have serious
consequences such as the emergence of new diseases or development of cancer.
Need vs. Want
Should we
actually design life based on choice or should we just leave everything to
chance? This is an important question that surrounds the use of gene-editing.
For some, gene-editing should be considered ethical since we are using this
technology to provide the next generation with genetic advantages that would
keep them from having diseases and even allow them to contribute significantly to
society. They see CRISPR as a need– an imperative to make a better world. On
the other hand, some would say that gene-editing is unethical since it plays
with life. It prioritizes subjective human preferences over natural processes
that have shaped the course of our evolution for millions of years. They look
at CRISPR as a want–a human vanity.
What We Should Do
As the CRISPR
technology develops, it is important that we make careful steps. Public
discussions and debates must continuously be done so that the whole society
would have clear ethical agreements. Strict
regulations and guidelines must also be imposed on the use of CRISPR to prevent
unintended consequences on the environment and human health. Research must also
be expanded by governments so that our knowledge of CRISPR would increase and
our awareness of its implications would widen.
CRISPR is a
powerful tool that can change the world but can also be destructive if we
become irresponsible with its use. Right now, we must proceed with caution so
that the potentials of CRISPR in improving our lives would not be laid to
waste.
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