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Australia takes lead, again
In a first-of-its-kind of decision Australian medical
regulator National Health and Medical Research Council (NHMRC) has issued
license to a Sydney firm to create cloned human embryo to obtain embryonic stem
cells. Sydney IVF, which received the government permission, has about 7,200
human eggs ready for research and has been given license to do only therapeutic
cloning.
The regulator said that if the Sydney based invitro-fertilization
company is successful in its endeavor, it will be the world's first.
This is the first time Australia has granted permission to
research on embryonic stem cells although Australia has been a pioneer on
research on adult stem cells.
In fact, Australia has been at the cutting edge of stem cell
research since long. Australian government has two laws that regulate the stem
cell research-The Prohibition of Human Cloning for Research Act 2002, which
draws the fundamental lines as to what is allowed and what is not; and The
Research Involving Human Embryos Act 2002, which sets out guidelines for
research involving the activities that are allowed. The net effect of this
approach is that Australia has chosen not to regulate basic research using human
embryonic stem cell lines, but instead regulate activities associated with their
creation.
The country has an envious position in stem cells business
not only because it has some of the best centers and labs for research but also
because it has some of the best talents and pioneering companies.
"Australian scientists are at the forefront of stem cell
research and in fact have been there for many years," says Prof. Silviu
Itescu, Executive Director at Mesoblast. A well-known Australian stem cell
company Mesoblast is publicly listed and for the last three-and-a-half years has
been commercializing technologies developed by world leading Australian
researchers from the Hanson Institute from Australia.
Australia, unlike some other countries in the region such as
China and Singapore that depends on Western trained and returned scientists to
do bulk of stem cell research, doesn't have to depend on overseas scientists.
It has all the talent within the country and in fact has seen its scientists
working and heading some other international research institutes across the
globe. India, Taiwan, Japan and to a larger extent south Korea, in this case,
have a strong line up of stem cell researchers that are domestically trained and
with the available local talent, are doing some amazing work.
A look at Mesoblast reveals how its researchers have
progressed in this domain. In late August 2008, scientists at Mesoblast launched
an off-the-shelf cell therapy product that was found to be effective for
interbody fusion of the cervical spine in the neck. And in the same month,
Mesoblast's researchers reported that their adult stem cell product
regenerated and regrew damaged knee cartilage in post-menopausal osteoarthritis.
Apart from the open and exciting stem cell research culture
in the country, Australia's pre-eminent position in the stem cell business
comes from the fact that government backing for the industry is very active
although funding is quite modest when compared to other Asian countries. "I
think the Australian government has been funding stem cell research because of
the belief that academic and industrial partnership will bring more benefit to
the Australian companies and research centers," says Prof. Itescu. "I
think that the institutional investor support has been tremendous. Although the
funding from federal government can increase and match if not exceed the funding
that governments in other Asian countries provide. "
The National Health and Medical Research Council (NHMRC)
provides funding for stem cell research, so do the various state governments. In
2007, NHMRC's total funding for all types of stem cell research, including
animal, human adult and human embryonic stem cell research, was somewhere around
A$50 million. Of that, a small proportion was specifically for human embryonic
stem cell research, states an official Australian Government note.
In the neighboring New Zealand, the government does not have
a policy in place for stem cell research. The country's strengths lie in
somatic nuclear transfer (SCNT) and the production of cloned and genetically
modified farm animals and in basic stem cell biology research. The funding in
New Zealand is very limited, both from governmental and private sources and New
Zealand researchers therefore can't compete in the main fields with the big
players, but they are thriving in niches and through overseas collaborations
using unique expertise and resources.
In New Zealand, most of the research in stem cells is
undertaken by the Ministry of Research, Science and Technology (MoRST). There
are also a number of other government agencies that have progressed work in the
stem cell domain and some private companies that too are researching on stem
cells. Companies such as AgResearch and Industrial Research have stem cell
programs of potential commercial value for agricultural and industrial
applications.
Living Cell Technologies (LCT) is one of the few companies
here researching on stem cells. Dr Paul Tan, CEO of LCT informs that the company
is researching the presence, proliferation and ability to differentiate into
islet beta cells of pancreatic progenitors in their microencapsulated porcine
islets. This could be a vital factor for the function and longevity of the
DiabeCell product.
"We are further currently researching the effects of our
preclinical microencapsulated porcine choroid plexus cell product (neurotrophin
producing cells) for the treatment of neurological diseases on neural stem cells
as a possible mechanism of action for the beneficial effects we have observed in
animal models of Stroke, Huntington's and Parkinson's disease," says Dr
Tan. "LCT is a world leader in the use of encapsulated porcine derived
neonatal islet implants. A prototype product of implanted encapsulted islets
remained viable and producing insulin in a patient after 10 years. Further, the
positive results from the ongoing clinical trial led to international media
interest and recognition. LCT is the first company to have the capability to
conduct human clinical trials under present regulatory guidelines."
The company is developing a product comprising encapsulated
neurotrophin producing cells that can be implanted to recruit endogenous
progenitor cells in the brain to the site of injury or disease and thereby
repair or regenerate brain tissue.
"This year we drew up a memorandum of understanding with
an international stem cell company to develop LCT technology for non-therapeutic
and therapeutic use with their of stem cell technologies," says Dr Tan.
Further, LCT entered into collaboration with a University in
Germany to use LCT's proprietary technology to stimulate neural crest stem
cells with the aim to treat Hirschsprung's disease, a congenital colon
motility disorder. This project is receiving joint financial support from New
Zealand and German government grants.
Then there is, Prof Richard Faull who is conducting world
leading basic research on human neural stem cell biology at the University of
Auckland. This work provides the basis for LCT's approach in the use of
implants of encapsulated neurotrophin producing cells for the recruitment of
natural progenitor cells for brain repair and regeneration.
AgResearch has a worldwide reputation in cloning of farm
animals, nuclear reprogramming and the derivation of ruminant species
embryonic-like stem cells. Further their research into tissue regeneration by
deer anthler stem cells holds great promise. Industrial Research recently
entered into a commercial collaboration with Singapore to test the utility of
purified glycocompounds in stem cell culture.
Although New Zealand has had its fair success in the stem
cell business, Dr Tan believes New Zealand cannot catch up with the rest of the
world. "New Zealand cannot catch-up with the US, Europe, Australia and Asia
in human embryonic stem cell research. There are, however, good opportunities
that New Zealand will become a recognized, innovative force in tissue stem cell
and tissue engineering therapeutics," he says.
Coming to the rest of Asia. India has no clear policy
regulating stem cell research but the country has its fair share of research
going on-though blazing success stories from India are yet to come by. Also,
the Indian regulations are by far more relaxed and quite supportive than some
other countries in the region. "However, there is a need for regulation of
individual investigator (doctor) initiated cell based therapies, as these tend
to be conducted in variance with international standards of clinical trials and
cell processing and the imponderables on safety and efficacy are not
scientifically addressed," says K V Subramaniam, President and CEO,
Reliance Life Sciences, a Mumbai-India based stem cell research and
biopharmaceuticals company.
Subramaniam says if India has to grow as a top stem cell
research hub, regulators would have to ensure that the:
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Conduct of research in stem cells consistent with ICMR
and DBT guidelines.
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Allogenic clinical trials are conducted based on
approvals of Drug Controller General of India.
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Efficacy of stem cell therapies are based on clinical
data generated through trials conducted as per ICH-GCP guidelines, which are
accepted by the international community.
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Processing of stem cells for clinical trials and
commercial therapies are carried out in a cGMP environment, approved by FDA.
In India several scientific departments and institutions of
the government, such as Department of Biotechnology, Department of Science and
Technology, Indian Council of Medical Research and Council for Scientific and
Industrial Research are promoting stem cell research. The priority areas of
research have been identified through discussions at various forums on basic and
applied sciences. Among the various programs being supported in embryonic and
adult stem cells research are: establishment of hESC lines, use of limbal stem
cells for repair of ocular surface disorders, isolation; purification and
characterization of hematopoietic, mesenchymal cells among others.
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Embryonic stem cells years away from therapy
-Dr Ina Sarel, Director of Research and
Development, Theravitae, Israel
Medicines only treat symptoms, not diseases. Repair
stem cell therapy offers a real solution to patients suffering from a
variety of diseases. It can be applied to cardiac disorders, nervous
system disease and renal failure, for example. Stem cell research has the
potential to transform disease treatment, reduce healthcare costs to
society and enhance quantity and quality of life for millions of patients.
Commercial success will generate significant business
opportunities. Literally, regenerative medicine is the birth of a new
sector of healthcare. Just like the dawn of the Internet, regenerative
medicine is generating new directions for industry, innovation and product
development. There is considerable debate as to which type of stem cells-embryonic
or adult-will produce the most effective therapies; there are advantages
and drawbacks to each. However, the safety and efficacy data of adult stem
cell treatments is published with increasing frequency whereas embryonic
stem cells are several years away from being used as a therapy. At
TheraVitae we derive adult stem cells from a patient's blood; our
technology improves heart function and blood flow to limbs that would
otherwise be amputated.
In Israel, the Israel Stem Cell Therapy Consortium, a group of medical
companies and academic research facilities, was created to coordinate the
efforts of local companies, scientists, and hospital research centers to
develop generic technologies for stem cell therapy. The Consortium had
been awarded a government grant of $15-20 million to develop the tools and
techniques for widespread development of stem cell-based therapies. |
Reliance Life Sciences is developing a wide range of novel
research-led, autologous and allogenic cell therapies and tissue-engineered
products to get into regenerative medicines business. Under the
"regenerative medicine initiative", the company has divided several
groups who work in areas such as embryonic stem cells, ocular stem cells,
haematopoietic stem cells and skin and tissue engineering. Cell-based therapies
from Reliance Life Sciences aim to meet unmet patient needs in the areas of
cardiac disorders, neural degeneration, spinal cord injury, metabolic disorders,
ophthalmic diseases, hematological diseases, oncological diseases, burns and
wound management, diabetic and venous ulcers, skin pigmentation disorders,
orthopaedic and cartilage disorders.
One of the newest companies in stem cell research in India is
Stempeutics Research, a Bangalore-based company focused on research,
therapeutics and therapy in the field of regenerative medicine.
The key challenges are all linked to safety
-Paul Bello, Scientific Program Manager, Stem
Cell Sciences, Australia
The current areas in which stem cell therapy
research is most active are: neurology (Alzheimers, Parkinsons
diseases), diabetes, cardiac conditions and spinal cord injuries.
There is also considerable research being done on iPS cells. The key
challenges faced by any firm working in the stem cell therapy space
are all linked to safety. In order to take such therapies to market,
they need to be accepted by the FDA. Any cells used in therapy must be
robust, consistent and efficiently scalable to GMP standards. This is
one of the areas that SCS is involved in. Scalability of cells
involves the culture of pure cell populations in suitable growth
media, which is serum-free. Animal product-free reagents are also
desirable for any potential therapeutic applications. SCS provides
such media under its CultiCell brand.
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B N Manohar, President of Stempeutics told BioSpectrum that
since its inception two years ago, Stempeutics has focused on two major types of
stem cells-Adult Stem Cells and Mesenchymal Stem Cells while also focusing on
human embryonic stem cells. It has developed cell characterization for purity
and identity by flow cytometry, functional assay for multipotency, process
validation for manufacturing, large scale cGMP complaint up-scaling of
mesochymal stem cells and quality control testing and quality assurance.
Stempeutics has established cell and tissue manipulation
facilities at Bangalore, Manipal (India) and Kuala Lumpur in Malaysia.
"India has massive potential for stem cell research as there is a very good
environment and we have things going for us," says Dr Manohar.
Stempeutics' research is into embryonic stem cells, stem
cell niches, self-renewal and signaling pathways, cancer stem cells, mesenchymal
stem cell biology, differentiation and transcriptional determination, diabetes,
cardiovascular, neuro-regenerative potential of adult stem cells, ocular stem
cells, and dental stem cells.
The island nation of Taiwan has a pro-stem cell policy that
has made the country a place of choice for stem cell research.
Dr Oscar Lee, who is with Department of Orthopaedics and
Traumatology, Taipei Veterans General Hospital, Taipei and Institute of
Biopharmaceutical Sciences, National Yang-Ming University, Taipei has been a
foremost stem cell researcher in Taiwan.
He says just like other Asia Pacific countries such as
Singapore, Hong Kong, and even Mainland China, the Taiwan government is putting
a lot of emphasis on the development of the stem cell industry.
"The government is pouring in considerable resources in
setting up and helping stem cell industries," says Dr Lee.
There are about 100-200 stem cell startups in Taiwan and this
number is quite huge considering the country has a population of just 23
million. Both domestic and international VCs are quite active in Taiwan offering
to fund anyone that comes up with an interesting project. Dr Lee predicts that
in 20-30 years Taiwan will be one of the most active countries in stem cell
research and the country to watch out for.
Taiwan has a lot going for it in the stem cell business. The
country is also benefiting from its researchers
returning to work in the country after retiring as professors and professionals
in top Western universities and top stem cell research labs across the world.
Taiwan researchers, informs Dr Lee, are working on usage of
stem cells to treat liver and cardiac diseases, gastroenterology, regrowing of
limbs and even human embryonic stem cells.
The major research theme of Dr Lee's lab is plasticity and
application of mesenchymal stem cells. Being an orthopedic surgeon as well as a
stem cell scientist, Dr Lee says he is particularly interested in developing new
application of mesenchymal stem cells to treat orthopedic problems.
His lab at National Yang-Ming University in Taiwan has
successfully isolated mesenchymal stem cells from human term umbilical cord
blood.
In addition, he says his research team has demonstrated the
differentiation potential of mesenchymal stem cells into hepatocytes in vitro.
The team also worked on an animal model of in utero transplantation of human
mesenchymal stem cells into mice to investigate in their vivo differentiation
potentials.
"We have demonstrated that human bone marrow-derived
mesenchymal stem cells are able to differentiate into progenies originated from
all three germ layers in vivo," Dr Lee says.
The team also investigated the growth and differentiation of
mesenchymal stem cells on Type 1 collagen nanofibers. "We have also looked
into the possibility of incorporating gene therapy with stem cells to further
enhance bone formation and found that concomitant overexpression of Cbfb and
Cbfa-1 can efficiently enhance osteogenic differentiation of MSCs,"
Dr Lee adds.
The combination of non-therapeutic businesses and
R&D of cell therapy is good business model
-Dr Chikafumi Yokoyaama, CEO, ReproCELL, Japan
Since a big bang of human iPS cells by Prof. Shinya
Yamanaka, Japan has been in the fever of iPS cells, which is supported
by Japanese government. iPS center, headed by Yamanaka, was
established in Kyoto and a relatively large amount of govermental
budget is prepared for iPS cell research, although it is far less than
that in US. Some Japanese pharamaceutical companies are interested in
iPS cells as a candidate of drug screening and development tool, but
not yet in cell therapy.
ReproCELL has been focused on the drug screening
and development applications by using ES and iPS cells. Our first
business target is a cardiotoxicity test service, QT prolongation, by
using monkey ES cell derived beating cardiomyocyte. It is now on sale.
Now, we are developing the same QT prolongation system by using human
iPS cells instead of monkey ES cells as our second new service that
will be launched in the spring of 2009.
I think that the fund raising is one of the most
severe challenges for stem cell therapy. Since, it is difficult to
estimate the money and time needed to reach the goals through clinical
trials, most hesitate to invest money. If a company such as Geron,
move forward to clinical trial of ES cell cell therapy, some investors
may change their opinions.
I think the most important thing for stem cell
companies is to start some business in non-cell therapy field as soon
as possible. Most of stem cell companies had the same business model
as the drug development type biotechnology company. However, it is
difficult to estimate the amount of money invested in cell therapy
business. It is quite different from the drug development business. I
think the combination of earning money in non-therapeutic business and
doing R&D of cell therapy is reasonable to overcome the financial
issue in the current situation.
In ReproCELL, three years ago we started some
non-therapeutic businesses including human ES cell medium, stem cell
related antibodies, clinical diagnostics related to transplantation,
and recently have launched the QT prolongation assay service. In
parallel, we have been continuing a research of cell therapy
"Ex-vivo expansion of hematopoietic stem cell by a low molecular
compound". Some stem cell companies have excellent technology
especially in cell culture and differentiation that must become seeds
of businesses. Stem cell business is not only a cell therapy but also
research reagent, drug screening tool, and order-made medicine.
In addition, these non-therapeutic businesses
should have a synergy effect on cell therapy. In our case, we have
been developing the differentiation technology from ES cell to
cardiomyocyte for QT prolongation business. However, if the
differentiation technology is brushed up further, it could be applied
for cell therapy in the future. I think the appropriate business model
is the key for success in stem cell business.
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Partnerships
Historically Asian research institutes have sought
partnerships and collaborations with North American or European institutes or
companies because West gives what Asians need-vast experience and in turn West
gains from generous fundings and strong support of both the government and
people in Asia and this makes job easier for both Western and Asian researchers.
India's Stempeutics has tied up with hospitals in Malaysia
where it has a research center. Stempeutic's partnership with Manipal Hospital
in Bangalore and a few other hospitals in both India and Malaysia have been
successful and now the company is seeking partnerships from other hospitals in
the Asia Pacific region.
Meanwhile, flushed with recent successes, Prof. Silviu Itescu
says Mesoblast is in the process of finalizing commercial partnerships both in
the US and in Asia Pacific. Mesoblast's sister company in the US Angioblast
has partnership with several companies in the cardiovascular space. "It is
looking to expanding that partnership and bringing more partnership to the
table," says Itescu.
Taiwan's Dr Lee says his research lab has tie ups with
various research centers around the world, most importantly with Kings'
College in London.
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"If India has to grow as a top stem cell research
hub, regulators would have to ensure that the:
-
Conduct of research in stem cells consistent with
ICMR and DBT guidelines.
-
Allogenic clinical trials are conducted based on
approvals of Drug Controller General of India.
-
Efficacy of stem cell therapies are based on
clinical data generated through trials conducted as per ICH-GCP
guidelines, which are accepted by the international community.
-
Processing of stem cells for clinical trials and
commercial therapies are carried out in a cGMP environment, approved
by FDA."
-K V Subramaniam, President & CEO, Reliance Life
Sciences, Mumbai, India |
Narayan Kulkarni & Sanjeev Jain
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