“On résiste à l'invasion des armées; on ne résiste pas à l'invasion des
idées” –
Victor Hugo (1802-1885), Histoire
d’un Crime, 1877.
Cellular
Dynamics (Nasdaq: ICEL) – Creating value from an idea whose time may just be
coming
The line I just quoted above
from Victor Hugo is the origin of those words people often attribute to him: ‘Nothing is more powerful than an idea whose time has come’. Hugo never said that. What he said was ‘An invasion of armies can be resisted; an invasion of ideas cannot be
resisted.’ That more accurate quote
comes from the final chapter of Hugo’s History of a Crime, where he describes the
1852 takeover of France by Louis-Napoleon Bonaparte (1808-1873), the Corsican
upstart’s nephew, who, leveraging widespread Bonapartist sentiment to the max, ended up crowning himself as Emperor Napoleon III. Hugo
didn’t like Napoleon III’s anti-democratic ways and chose to exile himself from
France until 1870, the year when the Emperor foolishly engineered a war with
Prussia that saw the French defeated in a matter of months and the Emperor’s
own reign ended in favour of the Third Republic. In concluding History of a Crime Hugo says that the invasion
of France by the Germans was bad, but the real winner in the long run was France
because it was fundamentally a country of ideas, not of arms, and the main
ideas it stood for – those of the French Revolution, which managed to make a
comeback with the Third Republic – were spreading out irresistibly throughout
the world. ‘What can be done against a revolution which
has so much right on its side? Nothing. To love it. That is what the nations
do. France offers herself, the world accepts her. The whole phenomenon lies in
these few words. An invasion of armies can be resisted; an invasion of ideas cannot
be resisted’.
So why do people always say ‘Nothing is more powerful than an idea whose time has come’? Because it’s true, as anyone who has watched
the battle of ideas which is science can attest. In this Biotech Buzz post I
would like to argue that stem cells are one of those ideas whose time has now
come, that great profits have the potential to come to those who back the idea
of stem cells as future therapies, and that one of the future winners may be
Cellular Dynamics (Nasdaq: ICEL), the stem cell manufacturer from Madison, Wi.,
which recently raised US$43m in an IPO.
Cellular Dynamics is the
creation James Thomson, the cell biologist from the University of Wisconsin at Madison
who became world famous in late 1998 when his lab became the first to isolate
human embryonic stem cells (click here for the Science paper which announced the
news). The Thomson lab’s work was a big step forward for science because it
looked like people could now start harnessing the pluripotency of stem cells and
with them treat all sorts of hitherto untreatable diseases. Stem cells are simply cells in the body with the ability to develop into a number of
different cell types. Since many diseases are caused by cells being lost or
damaged (think Type 1 diabetes and the loss of pancreatic islet cells), the apparent
ability of stem cells to regenerate what has been lost has enormous potential for
good. The trouble with the breakthrough from Thomson et. al. 15 years ago was
that their cells were pluripotent – capable of differentiating into almost all
cell types - but you had to create embryos to get them, and I don’t have to
remind you that a lot of us are not all that crazy about
messing with embryos. Mind you, it wasn’t just King James Bible-toting Christians
like me who had issues – it was scientists of all faiths or non-faiths who were
concerned about the tumorigenicity of embryonic stem cells. So in fact there
were two main ethical issues for the field to deal with. Think of embryonic
stem cells as the ‘invasion of armies that can be resisted’.
The beautiful part of the stem
cell story is that the ethical issues didn’t hold the field back. For a start,
people just focused on adult stem cells and started to use their
multi-potentiality (ie their ability to differentiate into some but not all
cell types) and the growth factors they secrete to make big scientific and
commercial strides. Just look at the Australian company which leads the stem
cell field globally, the Melbourne-based Mesoblast (ASX: MSB). It now has a
market capitalisation of A$1.7bn because its Mesenchymal Precursor Cells, grown
up from donated adult bone marrow, have yielded great clinical data in heart
failure and spinal disc repair and a massive 2010 partnering deal with Cephalon
that Teva inherited and, I believe, is going forward with. The work that went
into Mesoblast, however, didn’t win its founder, Silviu Itescu, the Nobel Prize
(which was fine because a Nobel these days only gets you a handshake with King Carl
XVI Gustaf of Sweden and 8 million Swedish kronor or ~US$1.1m, a lot less than the
quarter of Mesoblast stock which Silviu owns). The stem cell Nobel, awarded
last year, went to the man who created the real-deal breakthrough in the field
- Japan’s Shinya Yamanaka. In 2007 Yamanaka was able to show that normal
differentiated adult cells such as skin cells could be reprogrammed into ‘induced
pluripotent’ stem cells (iPS cells) using only four factors transduced into the
cells (click here for the Cell paper
that announced this). So you could create pluripotent stem cells without using
embryos. Goodbye, ethical issues. Hello future therapies.
Well, not quite. For the iPS cell
field there were quite a few technical issues to sort out related to which
factors to transduce and, most importantly, how to avoid the ‘footprint’, which included genetic
indicators of the vectors used to get the factors into the cells. Which
is where James Thomson and Cellular Dynamics comes in. In 2009 Thomson and
other collaborators invented a ‘footprint free’ technique for reprogramming
adult cells into iPS cells that involve the use of episomes (segments of DNA
that don’t integrate into that of the host cells) to deliver six reprogramming
genes (click here for the original paper). This provided a way to make clean iPS cells from any individual’s blood,
and then use them to manufacture differentiated tissue cells in industrial
quality, quantity and purity. Cellular Dynamics, the company founded by Thomson in 2004,
has spent the years since 2009 optimising this technology to the point where it
is rapidly becoming the ‘industry standard’ for iPS cells. I argue that this
technology has the potential to be the invasion of ideas that cannot be resisted in the stem cell field, even though people at
the moment are still worried about the footprint issue in terms ‘aberrant
epigenomic reprogramming’ – the idea that an iPS cell will have DNA hotspots resistant
to reprogramming that could hinder its therapeutic use (click here for a
relevant 2011 paper in Nature).
What will make is Cellular
Dynamics’s technology less likely to be resisted is the business plan. This company
isn’t a regular stem cell company with a pipeline of prospective cellular therapies
at clinical and preclinical. It is first and foremost a manufacturer of differentiated
cells whose main product is sold - for cold, hard cash - to academic groups and drug companies. These
customers now have, for the first time, genuine human cells with which to study
cellular processes and develop and test drugs. At the moment Cellular Dynamics makes
cardiomyocytes, neurons, hepatocytes and endothelial cells and more cell types will
become available all the time. All the big drug companies use cells from Cellular
Dynamics and in 2012 the company shipped US$5.2m of them. For the customers it
is money well spent because they can more easily avoid toxicities that may slip
through cells that only approximate rather than reproduce what real human cells
are like. US$5.2m may not seem like much for company capitalised at US$219m, but
business is brisk - in the June 2013 quarter revenue was US$2.8m versus US$1.3m
in the previous corresponding period. Moreover US$3.5bn gets spent every years
on cells for in vitro experiments globally
so Cellular Dynamics has plenty of room to grow. In short, Cellular Dynamics is
growing a business, and potentially a big business, while all
the time it gets better at making iPS cells and differentiating them. The company’s ideas will
continue to invade the field with every paper published that involved its
cells.
Differentiated cells for research
purposes aren't, however, the end of the story. The company also makes iPS cells
from specific tissue samples brought to them by customers. So, for example,
Cellular Dynamics won a US$16m contract in March from the California Institute for Regenerative Medicine (CIRM) to derive three iPS cell lines from each of
3,000 different individuals. The idea is for researchers to have a stem cell ‘bank’
that they can go to for stem cells relevant to diseases they are studying. Other
customers with particular cells they want to study or to use in cellular
therapy are coming to Cellular Dynamics to have iPS cells made of their candidate
cell so they can have as much of the cells as they need. Given enough time this
area of Cellular Dynamics may end up revolutionising stem cell banking and make
today’s cord blood collection industry look primitive. More importantly, it has
the potential to provide the basis for much of the cellular therapy that will be
commercialised in the future as stem cell developers turn to iPS cells as their
basic enabling technology.
Which brings us to what may be the
next stage of the journey. Cellular Dynamics announced in January that it was producing,
under cGMP, proprietary master cell banks of human iPS cells, where the donor
cells for starting material came from people with the HLA profiles (ie cellular
markers of ‘self’ as opposed to ‘non-self’ in the immune system sense) most
amenable to transplantation into unrelated recipients. This work will give
Cellular Dynamics a library of cells with the potential to develop into ‘off-the-shelf’
therapies for a range of disease conditions, whereas until recently people had
largely been thinking of iPS cells only for autologous use. Whether these new cells
banks will be accessible by customers the company didn’t say at the time. What the
iPS master cell bank development potentially gives Cellular Dynamics is the
ability to develop its own cellular therapies. That landmark may not be coming
for several years down the track, or it may not happen at all if the company
chooses to remain a seller of picks and shovels rather than a digger for its
own therapeutic gold. However given the progress that the iPS field has made
since 2007 it’s not unreasonable that Cellular Dynamics may become confident of
moving in that direction after a few more years of technology optimisation. That’s
because nothing is more powerful than an
idea whose time has come.
+61 (0)447 247 909
Twitter @Biotech_buzz
About Stuart Roberts. I started as an equities analyst at the Sydney-based Southern Cross Equities in April 2001, focused on the Life Sciences sector from February 2002. Southern Cross Equities was acquired by Bell Financial Group (ASX: BFG) in 2008 and I continued at Bell Potter Securities until June 2013. Over the twelve years to 2013 I built a reputation as one of Australia's leading biotech analysts. I am currently consulting to the Australian biotech industry. Before joining Southern Cross Equities I wrote for The Intelligent Investor, probably the most readable investment publication in Australia. I have a Masters Degree in Finance from Finsia. My hobbies are jazz, cinema, US politics and reading patent applications filed by biotechnology and medical device companies.
Previous Australian Biotechnology Buzz posts:
Cellular Dyamics (Nasdaq: ICEL), 3 September 2013
ImmunoCellular Therapeutics (NYSE MKT: IMUC), 27 August 2013
Immunomedics (Nasdaq: IMMU), 21 August 2013
Inovio Pharmaceuticals (NYSE MKT: INO), 24 August 2013
Merrimack Pharmcaceuticals (Nasdaq: MACK), 26 August 2013
Oncolytics Biotech (Nasdaq: ONCY), 22 August 2013
Pharmacyclics (Nasdaq: PCYC), 2 September 2013
Regulus Therapeutics (Nasdaq: RGLS), 23 August 2013
Sunshine Heart (Nasdaq: SSH), 28 August 2013
Synta Pharmaceuticals (Nasdaq: SNTA), 1 September 2013.
Disclaimer. This is commentary, not investment research. If you buy the stock of any biotech company in Australia, the US or wherever you need to do your own homework, and I mean, do your own homework. I'm not responsible if you lose money.
Cellular Dyamics (Nasdaq: ICEL), 3 September 2013
ImmunoCellular Therapeutics (NYSE MKT: IMUC), 27 August 2013
Immunomedics (Nasdaq: IMMU), 21 August 2013
Inovio Pharmaceuticals (NYSE MKT: INO), 24 August 2013
Merrimack Pharmcaceuticals (Nasdaq: MACK), 26 August 2013
Oncolytics Biotech (Nasdaq: ONCY), 22 August 2013
Pharmacyclics (Nasdaq: PCYC), 2 September 2013
Regulus Therapeutics (Nasdaq: RGLS), 23 August 2013
Sunshine Heart (Nasdaq: SSH), 28 August 2013
Synta Pharmaceuticals (Nasdaq: SNTA), 1 September 2013.
Disclaimer. This is commentary, not investment research. If you buy the stock of any biotech company in Australia, the US or wherever you need to do your own homework, and I mean, do your own homework. I'm not responsible if you lose money.
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