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Stem Cell Therapy: The Holy Grail of Medicine
Stem cell therapy is the new buzz in medical corridors with
'miracle' cures being reported everyday. Nancy Singh analyses the promises
it holds for various diseases and the growing market for it.
Four-month-old
Aarohi Bhatt recently created medical history for being cured of a rare heart
condition believed to be untreatable. The cause of her cureStem Cell Therapy
(SCT) using her father's blood at Frontier Lifeline Hospital, Chennai. Besides
being a difficult surgery, it was for the first time in the world that SCT was
successfully done on a child so young.
Stem cell therapy is said to be expensive, however, considering that the effects
of treatment are long lasting, without requiring expensive repetitive treatment,
this seems affordable. Frost & Sullivan estimates that the annual cost of
$2,500 per patient for SCT, at the manufacturer's level, is an average cost
distributed over several years.
For large scale of production of stem cell lines, consistency
is the key factor. Dr Mahendra Rao of Stem Cell Biology Unit, Gerontology Research
Center, US, agrees, "Researchers must be able to repeat each other's experiments
and establish a baseline set of quality controls that will be required for large
scale therapy."

Corneal limbal epithelial cells
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Differentiated human neurons
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Spherical shaped bone marrow mononuclear cells
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Human mesenchymal cells
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Human embryonic stem cells
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Stem cells offer promising treatment for genetic diseases
such as diabetes, where they can be a plausible alternative to recombinant proteins
available in the market. "The market size for diabetes is greater than
Parkinson's, because in Parkinson's the latest clinical trials are not assuring,
while trials for diabetes are easy because engraftment is easy," believes
Alan Colman, CEO, ES Cell International, Singapore.
Spinal repair is another area with a high patient potential. In the US alone,
there were over 2,00,000 patients in 2004, and the potential value for SCT is
estimated to be $4 billion in a Frost & Sullivan study.
Alzheimer's disease is another area with vast unmet needs that stem cell manufacturers
are targeting. Assuming a penetration rate of 50 per cent in the current patient
population base in the US, Alzheimer's therapies could be worth approximately
$2 billion, according to another Frost & Sullivan study.
Similarly, various forms of cancer, coronary artery disease, and heart therapies,
ophthalmology, tissue engineering, organ transplantation and gene therapy all
offer tremendous promise to stem cell manufacturers.
Show Me the Money!
What would attract investors and venture capitalists to SCT?
"Investors are bullish on stem cell products for diseases that cannot be
cured by non-cell products. Ideally, investors are interested in stem cells
products that have application in curing diseases that have plenty of unmet
need,like in spinal cord injury, Parkinson's disease, cardiovascular diseases,
diabetes, cornea regeneration and off late AIDS cure," says Linda F Powers,
MD, Toucan Capital, a leading US investor in stem cells and regenerative medicine.
She believes that since most companies are focusing more on research, they tend
to ignore the 'feasibility in terms of transportation and distribution'. "Stem
cell products that are less cumbersome at the point of care, are easy to handle
and those that are feasible for storage attract immediate investment,"
she adds.
For Ophthalmology
Leading organisations using cultured stem cell transplant
are LV Prasad Eye Institute (Hyderabad), Sankara Nethralaya (Chennai), AIIMS
(New Delhi), and Aditya Jyot Eye Hospital (Mumbai). These institutes grow stem
cells in a culture medium in the lab and transplant them to patients suffering
from chemical burns and ocular diseases. LV Prasad Eye Institute is the first
hospital which has met with success in using cultured stem cells to treat corneal
opacity and blindness. They have passed the clinical trial stage and treated
over 250 patients with a 70 per cent success rate.
Stem cells exist in various regions of the eye, throughout one's life. So far,
stem cells can be found at the outer edges of the cornea (the outer clear part
of the eye covering the iris and pupil), the conjunctiva (the thin, moist membranes
that covers the inner surface of the eyelids and the outer surface of the eyeball),
as well as the ciliary margin (the tissue that lies just behind the iris).
The purpose of corneal or limbal stem cells is to maintain a healthy eye surface
and replace cells that are lost and blinked away. The stem cells of the cornea
are located at the limbus (the thin area between the clear cornea and the white
sclera of the eye). These limbal stem cells can be transplanted for severe eye
injuries. During this outpatient procedure, some limbal stem cells are extracted
from the healthy eye of the patient (autograft), or a donor's eye (allograft)
or cadaver, and then transplanted to the affected eye.
In a successful transplant, limbal stem cells or corneal stem cells will produce
a new healthy layer of cells in the patient's eye. The success rate varies from
25 per cent to 70 per cent, depending on the underlying condition of the affected
eye.
"The decision to use an autograft or allograft depends
on the patient's condition. For example, an autograft would not
be possible in a patient diagnosed with aniridia, wherein both eyes
would be deficient of limbal stem cells. In cases of a unilateral
chemical injury, the normal other eye can be used to harvest the
limbal stem cells for cultivation and can then subsequently be transplanted
into the affected eye. However, in cases of bilateral chemical burns,
the relative with an unaffected eye is a better choice." informs
Dr Vandana Jain, Head of Department and Consultant, Cornea, Cataract
and Refractive Surgeon, Aditya Jyot Hospital, Mumbai.
Opines Dr Radhika Tandon, Professor of Ophthalmology, Dr Rajendra Prasad Eye
Institute of Ophthalmic Sciences, AIIMS, "For corneal transplant, India
is on par with any other country in the world."
Currently, research is ongoing on retinal stem cells (stem cells of the retina),
where scientists are in the process of trying to culture them in labs. In future,
it may help to cure diseases like retinal dispigmentosa, a retinal degeneration
for which currently there is no cure.
In another breakthrough research, an Indian institute in collaboration with
Japanese Nichi-In Centre for Regenerative Medicine (NCRM) has formed a synthetic
culture medium which multiplies corneal limbal stem cells. "For the first
time, we have been able to culture corneal limbal stem cells without any animal
protein or human amniotic membrane," informs Dr Samuel Abraham, Director,
NCRM's branch in Chennai.
| South Korean researcher, Dr Hwang Woo Suk, who won
world acclaim as the first scientist to clone a human embryo and extract
stem cells from it, admitted to 'faking' results. This has dampened spirits
after giving hope to millions, by making a 37-year-old paralysed woman,
walk again. Dr Hwang and his team's production of stem cells from cloned
human embryos in 2004 was considered a major step toward treating conditions
like Alzheimer's disease and spinal cord injuries.
He injected stems cells isolated from umbilical cord
blood into the injury area of the woman who had sustained a T-10 complete
injury from a fall. Unfortunately, according to recent reports, after
her a second SCT, her condition has greatly deteriorated. She is now unable
to sit erect for long time. Even after undergoing another treatment, she
is unable to move.
Doctors suggested she contracted an infection the second
time due to either procedural aspects or bacterial contamination of the
transplanted cells. As a result, the surrounding tissues have hardened.
The researcher confirmed that in 2002 and 2003, two of
his researchers donated eggs and a hospital director paid about 20 other
women for their eggs.
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For Spinal Cord Injuries
SCT at Lifeline Multi-Speciality Hospital, Chennai enabled 25-year-old Akbar
Ali who injured his spinal cord in a fall to walk normally again. When he was
admitted to a hospital in Abu Dhabi, a plate was fitted to treat his spinal
fracture, but this did not offer him any abilities. The accident resulted in
paralysis from the waist down.
"This is the first time that Indian doctors have resorted to SCT to cure
spinal cord problems and the second time in the world of literature," said
Dr JS Rajkumar, Chief Surgeon, Lifeline Multi-Speciality Hospital,Chennai
Ali underwent autologous SCT in December 2006. The Lifeline Stem Cell Team aspirated
100ml of bone marrow fluid from the hip bone, isolated the stem cells, processed
in NCRM, as per the technological know-how from Dr Terunuma Hiroshi of Biotherapy
Institute, Tokyo, Japan and 20 ml of this concentrate was injected into his
spinal fluid. Soon, he was able to walk on his own.
"This has showcased the ability of SCT to bring people with paraplegia
back to normalcy in a fast and effective manner," says Dr R Ravi Kumar,
Cardiologist and STC Project Co-ordinator, Lifeline Multi-Speciality Hospital,
Chennai.
Lifeline Hospital is now pursuing an active bone marrow derived stem cell programme
for spinal injuries and currently seven patients are undergoing this treatment.
| On the surface, the possibilities for stem cell therapy
seem limitless. Can't we use stem cell technologies to replace any diseased
or damaged tissue in the body? To answer this question, researchers must
figure out the true potential and limitations of stem cells. Some questions
currently being addressed include:
How long will a stem cell therapy last?
The reason we age is because our cells do. So will adult
stem cells used for treatment age faster? As of now, scientists do not
know this.
Can we ensure that SCT won't form tumours in
the body? Embryonic stem cells are naturally programmed to divide
continuously and remain undifferentiated. To be used successfully in therapies,
embryonic stem cells must be directed to differentiate into the desired
type of tissue and ultimately stop dividing. Any undifferentiated embryonic
stem cells that are placed in the body might continue to divide in an
uncontrolled manner, forming tumors-known as 'teratomas.
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For Cardiology & Neurology
"We
still have 20 patients in waiting, but we are very choosy"
- Dr Sanjay Cherian
Director and Staff Surgeon
Frontier Lifeline,Chennai
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Treatment of heart problems using stem cells was first reported
in March 2005 by AIIMS in New Delhi when trials were conducted on 35 patients.
There was no mortality reported and all patients were brought in at a stage
where surgery was ineffective. After six months, 56 per cent of the affected
(read dead muscle) area injected with these cells showed improvement. After
18 months, this went up to 64 per cent.
The Stem Cell Facility at AIIMS was established in 2005 to
explore the safety, feasibility and the efficacy of autologous (from the body
itself) hematopoietic and cord blood stem cell transplantation in degenerative
diseases. As of now, 360 patients have undergone SCT for various diseases.
At AIIMS, presently SCT is performed at a pilot scale for many of the degenerative
diseases like dilated cardiomyopathy, myocardial infarction, dilated cardiomyopathy
and acute ischaemic stroke. "Acute myocardial infarction has moved a few
steps above the pilot scale studies. The main focus is mainly on adult stem
cells and umbilical cord blood stem cells at our Centre," says Dr Sujata
Mohanty, Assistant Professor, Stem Cell Facility, AIIMS. Currently in phase-II
trials for using autologous mononuclear cells (from the body) for various heart
disorders, SCT is being administered to eight patients.
The R&D department of Frontier Lifeline Hospital, Chennai is working in
collaboration with Tirupati-based C Venkateswarlu Institute for SCT. The technique
used to separate these mononuclear cells is 'apheresis', which helps in isolating
the stem cells from the bone marrow that differentiate only into heart cells.
Though such therapies have been conducted earlier, what is different now is
the number of children opting for this has swelled. Frontier Lifeline has conducted
SCT on a five-year-old girl suffering cardiomyopathy. In this case, the only
alternative was heart transplant, for which no heart was available.
"All patients are under six-month review and hitherto have not shown any
complications," informs Dr Sanjay Cherian of Frontier Lifeline. "We
still have 20 patients in waiting but we are very choosy." The Hospital
has started an active programme in SCT for heart failure which is performed
as minimally invasive heart surgery.
Meanwhile, the Manipal Education and Medical Group's (MEMG) newly spun-off entity,
Stempeutics, is set to begin the country's first formal, full-scale clinical
trials using stem cells. "We focus on developing therapies using adult
human mesenchymal stem cells to treat people with damaged heart tissue, spinal
injury, ischaemic limb (with lost circulation), to be followed by optic nerve
injury," according to Dr Ramananda Nadig. COO, Stempeutics.
Stempeutics has developed patented technology of isolation and culture of mesenchymal
stem cells derived from the bone marrow which supports long-term proliferations
of these cells and hence do not require repeated collection of bone marrow reducing
the cost and thus making therapy affordable. One batch production of mesenchymal
stem cells can easily target around 150 patients at one time and hence clinical
trials become easy to perform.
"Pre-clinical studies in animals and toxicity studies are over and we are
now embarking on the first-of-its-kind phase-II clinical trial for acute myocardial
infarction, peripheral arterial diseases, spinal cord injury and stroke soon,"
informs Dr Totey.
He expects that, in another year-and-a-half for trial results and regulatory
approval for the treatment, these cell therapies should be available 'off the
shelf' by 2008-09 across the country's tertiary hospitals. MEMG has initially
invested Rs 5 crore in creating the cell culture room, cGMP lab, quality, testing
and screening facilities in a portion of its Manipal Hospital campus in Bangalore.
Internationally, doctors in Germany reported the successful use of a patient's
own adult stem cells from bone marrow for regenerating tissue damaged after
a heart attack in July 2001. They injected the man's own bone marrow stem cells
into his damaged heart muscle. Ten weeks after treatment, the damaged area of
heart tissue had considerably reduced, replaced by new cells, and the function
of the patient's heart had increased by 20-30 per cent. The authors note that
their results demonstrate that transplantation of human autologous adult
stem cells is possible under clinical condition. The use of the patient's
own adult stem cells from bone marrow or muscle to treat damage from heart attack
is also in clinical trials in France and the US.
French physicians implanted skeletal muscle stem cells back into the patient;
the encouraging result after eight months' follow-up underlines the potential
of this new approach using adult stem cells. Furthermore, in February 2007,
surgeons at Madrid Hospital in Spain claim to be the first to have used stem
cells from a patient's fat tissue extracted through liposuction to treat
the patient's heart.
The patient, a 67-year-old man, suffered from angina and
damaged coronary arteries. Plastic surgeons first performed liposuction on the
patient's abdomen to remove the fat and extract and purify the stem cells. Heart
surgeons then injected stem cells into the heart, where doctors hoped that they
will turn into additional heart muscle and blood vessels. The fat cells were
chosen for the procedure because they do not need to be cultivated for three
weeks before use, as do stem cells from bone marrow.

Arohi underwent stem cell therapy at Frontier Lifeline
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Akbar Ali (in blue) with team of experts at Lifeline Hospital
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For Diabetes
"For
the first time, we have been able to culture corneal limbal stem cells without
any animal protein or human amniotic membrane"
- Dr Samuel Abraham
Director, NCRM, Chennai
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Posterior tibial artery, anterior tibial artery and peroneal
artery are the three major blood vessels supplying blood to the foot and leg.
The posterior tibial artery which forms major part of the foot and the backside
of the calf was totally occluded in a 68-year-old diabetic patient with limb
ischemia and had been advised an amputation of the affected area, because there
was no possibility of performing a bypass surgery to salvage the limb as the
distal portion of the vessel was occluded. At this juncture, Chennais
Vijaya Health Centres vascular team after scanning publications of international
journals, resorted to this treatment. Though for other kinds of diseases such
treatments have been done in other institutes in India, for diabetes this has
not been reported and, in that sense, it was the first time in India.
Dr Abraham explains, "In this treatment, the patient's bone marrow was
tapped under general anaesthesia and 100 ml of bone marrow was aspirated. The
bone marrow stem cells were isolated and suspended for injection as per cGMP
protocols at NCRM." These isolated cells were then injected to the calf
muscle affected portion two times in an interval of one month. From the time
of the administration of the injection, the healing started very rapidly and
healthy granulation started covering the previously ischemic portion of the
limb and close to 40 per cent of the foot area, 20 per cent of calf area and
100 per cent of the lateral wound region were covered by skin. The remaining
portion was treated with skin grafting and could successfully heal. The patient
is able to use her left lower limb as much as the right side.
Incidence of diabetes is rapidly increasing in India and is likely to see more
patients. "In such patients, when there is no feasibility of a revascularisation
by bypass surgery, and amputation is the only option, we can say that autologous
bone marrow stem cell therapy would be suitable and safe," says Dr Abraham.
In another case, bone marrow transplant has cured experimental diabetes in mice.
Can it do the same in humans? National Center for Cell Sciences (NCCS), Pune
is still seeking answers. "In an effort from bench to bedside, NCCS is
underway to translate the research from the scientists' bench to the patients'
bedside," says Dr RR Bhonde, Deputy Director, NCCS, who has already proved
how bone marrow transplant cures experimental diabetes in mice by regeneration
of pancreas, the results of which he presented at SCRFI.
NCCS has now initiated human experiments as a cure for diabetes. The stem cells
are isolated from bone marrow that is taken from various patients after an ethical
clearance. Several samples are taken and a process is initiated to standardise
the expansion of stem cells and differentiate them into pancreatic or insulin
producing cells. While there is some time before human clinical trials are launched,
results have been encouraging from these human experiments, Bhonde adds.
Liver Failure
Lifeline is planning to use SCT for patients needing liver transplants in association
with NCRM. The programme conforms to ICMR guidelines on stem cell therapy and
does not involve usage of allogenic, immunogenic, animal protein or fetal materials.
The biological materials injected are bacteria- and viral-free and are derived
from patients' body cells and are non-reactive.
Problem Areas
If various initiatives and projects have to be sustained, then India needs to
address shortage of trained manpower in SCT. "While it is easy to build
great infrastructure, we have failed in building human resources. We are far
behind China in this aspect," laments Dr MK Bhan, Secretary, Department
of Biotechnology, Government of India,while addressing the first annual Stem
Cell Research Fourm of India (SCRFI).
"In India we do not encourage innovation among young scientists. Though
we have so many genetic engineers, there is inadequate focus on R&D,"
adds Dr Inder Verma, Professor of Molecular Biology, Salk Institute in California.
Efforts have been made to bring clinicians and basic researchers together for
interaction by organising a number of clinical research workshops, extensive
training programmes, brainstorming sessions, which has resulted in the formation
of the SCRFI
Dr Donald W Fink, Biologist and Regulatory Review Scientist at the US FDA, believes
that it would be ideal to have a single international body to overlook all regulatory
aspects of drug approvals which could have one common procedure to meet the
regulatory requirements and drug approval standards. We have just started learning
the first chapter in SCT and it is a long way to go before we unravel the mystery,
but nevertheless it may change the course of therapy as we know it.
nancy.singh@expressindia.com
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