Noting some of the more selfish and sinister practices of
humans seeping into the 3D printing ecosystem and even having been on the
receiving end of some of it personally, some days it can be hard to look for
the good and find the joy. Disappointing experiences are a part of life,
though, as is tragedy and life goes on, even when it doesn’t.
Looking for inspiration among those consistently working for
the greater good I turned to the field of 3D bioprinting — a discipline that
undoubtedly promises so much for humanity in myriad of ways. The ultimate goal
of 3D printing compatible organs for patients in desperate need of transplant
has been cited over and over and over again since the first breakthroughs in
the field around the turn of the century, and is, indeed a noble aim that a
number of esteemed research and development (R&D) laboratories across the
globe claim to be working towards as they develop new animate printing
techniques with living cells for a wide range of specific applications.
The ability to precisely create, manipulate and sustain
living tissues will signify a true paradigm shift in the provision of
personalised health care and extending life for many. I say ‘will’, because
while creation and manipulation has largely been proven there is still a
question mark over sustaining the tissues once they have been formed. Efficacy
still has to be proven over time too.
I was lucky enough to hear Gabor Forgacs give a presentation
on his pioneering work in the field of bioprinting recently, and to speak with
him one on one subsequently. The man, who is the founder of Organovo and Modern
Meadow, quite simply, is a genius; and passionate in his approach and opinions
I found.
He pretty much dismissed the hyped headlines about 3D
printing complete organs: “We can NOT print a whole organ – if anyone tells you
they can, they are lying.” Qualifying this he assured it was not impossible in
the long term, but that no one is even close to that right now. He also gave
his own opinion: “I personally do not believe that we will ever be able to
print (or use any other engineering technology) to produce exactly the organ
required.” To back this up, he cited evolution taking many millions of years to
arrive at this very beautiful, extremely efficient organ — the human heart. It
is extremely complex, and resilient. Did you know that yours will beat, on
average three billion times in your lifetime? But then Gabor threw a curve ball
when he asked: “Who says it is the best design?”
Thus, he explained, while today’s biogengineers are
brilliant “we can’t build a [functioning] replica of the heart, and I don’t
think we ever will. BUT, what we can do, is use our engineering ingenuity, and
biological understanding to put something together that will function like — or
even better than — the human heart. Using your own cells so it won’t be
rejected – that’s where I see bioprinting going.”
Having dealt with his vision of the future of bioprinting,
almost as a chore, Gabor was keen to get back to the present. This is where his
passion quite obviously lies — making a difference now. In this regard he
outlined a number of areas where bioprinting is proving capable of doing just
that, even if it doesn’t sound as exciting printing full body parts.
Primarily he believes that using bioprinted tissues as a transition
step in the development of new drugs — between pre-clinical trials (on animals)
and full clinical trials (on humans) — is a huge advantage for both the
patients and the drug companies. He cited how often the biggest stumbling block
in drug development comes at this stage in the process because “animal tissue
is not characteristic for human behaviour.” Thus, even if a new drug has shown
positive results in animals (a huge ethical question of its own) there is no
guarantee that it will transition
successfully to human trials. As a result the risks are still high for patients
participating in the trials and the losses, if it fails, can be massive for the
drug company (circa $500 million if a complete failure is fairly average) and
that does not take account of the time wasted either.
Gabor believes that “THIS is what 3D bioprinting can offer
resolution to now.” If you utilise engineered human tissue between pre-clinical
animal trials and human clinical trials it can illustrate a human toxic
response for a new drug ahead of clinical trials and save the drug development
project huge amounts of time and money, but, more important than that, it
prevents the drug test having an adverse affect on a patient and/or offering
false hope.
And the ultimate goal here is to eliminate animal testing
completely, the ethics of which is questioned by many — to the point of
violence in extreme cases. Even more so when the experiments are conducted on
animals for testing beauty products.
As Gabor explained, TODAY Organovo, right now, can print
human liver tissue with architecturally, compositionally and functionally
correct make-up. When this is interfaced with a drug when taken orally it is
capable of demonstrating a toxic response and thus point to a toxic response
across the rest of the complex human system. “It may not be the application
everyone is getting excited about but it’s real and, actually, the implications
are HUGE for humanity,” concluded Gabor on this subject.
And, in the near term, Gabor believes that the small scale
bioprinting that is possible now will support some reconstructive surgeries. He
cited blood vessels at this point, and the number of patients globally
suffering from clogged arteries and requiring bypass surgery, with one famous
ex-president as his specimen. There are four arteries from other parts of the
human body that are compatible with bypass surgery. One Bill Clinton has used
all four — if he needs a fifth, he’s dead. That’s it. Four strikes and you’re
out ….unless you use bioprinting!
Gabor reports that Organovo is close to achieving this
application of bioprinting part of an artery for bypass surgery and believes it
will ameliorate the problem significantly.
I don’t know about you, but having experienced a grandparent
and an Uncle that have both undergone bypass surgery, and learning that
potentially my kids may have a better outcome — I think that’s huge!
Returning to the bioprinted liver tissue potential, Gabor
went on to explain that this could still help patients with significant liver failure
that are waiting for a donor not knowing if they would live of die. Once again
dismissing the entire organ idea, he posited how by taking a small piece of
liver — what he called an “organoid” and implanting it, there was an increased
chance of improving and extending the life of the existing bad liver,
potentially providing enough time to find a donor.
With more than 100,000 people waiting for a kidney
transplant in the US alone, where only 1 in 6 will get one, this is an
encouraging, albeit partial, solution to a very serious situation that is only
going to continue to get worse. Any hope has to be better than no hope?
This is truly a great read for me. I have bookmarked it and I am looking forward to reading new articles. Thanks again and good luck. Civil Engineering Now follow-up the keyword Denver Civil Engineering Keep up the good work!
ReplyDeleteThank you pertaining to submitting the truly great written content. We all needed similar to this kind of. I ran across this kind of relaxing interesting, if at all possible someone. We all benefit which you developed this kind of great submit to aid many of us have an overabundance comprehension of this kind of subject matter. Today just click here wordpress backup Good luck along with keep on the nice performs.
ReplyDelete