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AN EYE FOR AN EYE: Using stem cells to treat damaged eyes and a rare skin disorder
October 23, 2007Doctors and scientists in Italy have shown how stem cells can be used to treat damaged eyes and, in combination with gene therapy, a rare and debilitating skin disease.
Professor Michele De Luca of the University of Modena and Reggio Emilia described the work to an international meeting of stem cell scientists in Milan (30 Sep - 2 Oct, "Challenges in Stem Cell Differentiation and Transplantation") organised by the European Science Foundation's EuroSTELLS stem cell programme in conjunction with the National Research Council of Italy.
Stem cell therapy involves the use of stem cells - 'blank' cells ('toti- or 'pluripotent') that have not differentiated into specialised cells - to generate new tissues or organs. While widespread stem cell therapy lies some way in the future, Professor De Luca pointed out that it has been used already for many years in the treatment of burns. Many tissues of the body are continuously regenerated by their own population of stem cells. In the skin, such cells are called holoclones and for decades doctors have taken small samples of these cells from burns patients and cultured the cells into new skin that can be grafted onto the wound.
Professor De Luca's team showed that cells of the transparent outer covering of the eye, the cornea, are constantly being replaced by new cells deriving from an area surrounding the cornea called the limbus. The cells differentiate into corneal epithelium and migrate to the cornea.
"If the cornea is damaged severely by a chemical burn or infection, for example, it can become opaque and necessitates a transplant," Professor De Luca told the meeting. "However, a transplant will only be successful if the patient's limbus has remained intact so that it can continue to replenish the new cornea."
For many years doctors did not understand why some transplants failed - because they did not appreciate the requirement for the limbus.
In cases where the limbus is destroyed there has been little hope to restore the patient's sight. Professor De Luca's team decided to take a leaf from the way that burns are treated and grow a new cornea from limbar stem cells taken from the healthy eye.
By removing a small sample of these cells it was possible to culture a new cornea and graft it on to the damaged eye. The team showed that of 240 patients who were operated on in this way, the cornea regenerated successfully in 70% of cases.
The researchers then turned their attention to a rare but debilitating genetic disease of the skin resulting in a syndrome known as Epidermolysis Bullosa, in which the skin is highly fragile and prone to blistering due to faulty proteins that effectively anchor the surface layers of skin to the body.
In one form of the disease there is a mutation in one of these anchoring proteins called laminin 5. The Italian researchers obtained consent to carry out a small-scale trial of a novel gene therapy using skin holoclones on one patient, a 37-year-old male, on small part of his body .
"Because the patient's body was so badly affected it was difficult to isolate any stem cells from his skin," Professor De Luca told the conference. "Most people have between seven and ten per cent of holoclones. Our man had none. Eventually we found a few in the palms of his hand and cultured them from a biopsy."
The team then used gene therapy to insert the correct laminin gene into the growing cells and grafted the new tissue onto the patient's body. The graft was successful and after several months the skin remained to all intents normal, without the blistering and flaking.
"This demonstrates that it is possible to use stem cells in gene therapy for genetic skin disorders," Professor De Luca said.
EuroSTELLS is the European Collaborative Research (EUROCORES) programme on "Development of a Stem Cell Tool Box" run by the European Medical Research Councils (EMRC) Unit in the European Science Foundation. ESF provides scientific coordination and support for the networking activities of funded scientists through the EC FP6 Programme, under contract no. ERAS-CT-2003-980409. Research funding is provided by the participating national organisations.
European Science Foundation
Professor De Luca's team showed that cells of the transparent outer covering of the eye, the cornea, are constantly being replaced by new cells deriving from an area surrounding the cornea called the limbus. The cells differentiate into corneal epithelium and migrate to the cornea.
"If the cornea is damaged severely by a chemical burn or infection, for example, it can become opaque and necessitates a transplant," Professor De Luca told the meeting. "However, a transplant will only be successful if the patient's limbus has remained intact so that it can continue to replenish the new cornea."
For many years doctors did not understand why some transplants failed - because they did not appreciate the requirement for the limbus.
In cases where the limbus is destroyed there has been little hope to restore the patient's sight. Professor De Luca's team decided to take a leaf from the way that burns are treated and grow a new cornea from limbar stem cells taken from the healthy eye.
By removing a small sample of these cells it was possible to culture a new cornea and graft it on to the damaged eye. The team showed that of 240 patients who were operated on in this way, the cornea regenerated successfully in 70% of cases.
The researchers then turned their attention to a rare but debilitating genetic disease of the skin resulting in a syndrome known as Epidermolysis Bullosa, in which the skin is highly fragile and prone to blistering due to faulty proteins that effectively anchor the surface layers of skin to the body.
In one form of the disease there is a mutation in one of these anchoring proteins called laminin 5. The Italian researchers obtained consent to carry out a small-scale trial of a novel gene therapy using skin holoclones on one patient, a 37-year-old male, on small part of his body .
"Because the patient's body was so badly affected it was difficult to isolate any stem cells from his skin," Professor De Luca told the conference. "Most people have between seven and ten per cent of holoclones. Our man had none. Eventually we found a few in the palms of his hand and cultured them from a biopsy."
The team then used gene therapy to insert the correct laminin gene into the growing cells and grafted the new tissue onto the patient's body. The graft was successful and after several months the skin remained to all intents normal, without the blistering and flaking.
"This demonstrates that it is possible to use stem cells in gene therapy for genetic skin disorders," Professor De Luca said.
EuroSTELLS is the European Collaborative Research (EUROCORES) programme on "Development of a Stem Cell Tool Box" run by the European Medical Research Councils (EMRC) Unit in the European Science Foundation. ESF provides scientific coordination and support for the networking activities of funded scientists through the EC FP6 Programme, under contract no. ERAS-CT-2003-980409. Research funding is provided by the participating national organisations.
European Science Foundation
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The generation of new nerve cells in the brain is regulated by a peptide known as C3a, which directly affects the stem cells' maturation into nerve cells and is also important for the migration of new nerve cells through the brain tissue, reveals new research from the Sahlgrenska Academy published in the journal Stem Cells.
Umbilical cord blood stem cell transplant may help lung, heart disorders
Two separate studies published in the current issue of Cell Transplantation (18:8), - now freely available on-line have shown that transplanted human-derived umbilical cord blood (UCB) stem cells transplanted in an animal model had positive therapeutic effects on specific lung and heart disorders the animal models.
Gene mismatch influences success of bone marrow transplants
A commonly inherited gene deletion can increase the likelihood of immune complications following bone marrow transplantation, an international team of researchers reports in the November 22 advance online issue of Nature Genetics.
New research shows versatility of amniotic fluid stem cells
For the first time, scientists have demonstrated that stem cells found in amniotic fluid meet an important test of potential to become specialized cell types, which suggests they may be useful for treating a wider array of diseases and conditions than scientists originally thought.
First reconstitution of an epidermis from human embryonic stem cells
Stem cell research is making great strides. This is yet again illustrated by a study carried out by the I-STEM* Institute (I-STEM/ Inserm UEVE U861/AFM), published in the Lancet on 21 November 2009. The I-STEM team, directed by Marc Peschanski has just succeeded in recreating a whole epidermis from human embryonic stem cells.
Bone Implant Offers Hope for Skull Deformities
A synthetic bone matrix offers hope for babies born with craniosynostosis, a condition that causes the plates in the skull to fuse too soon.
Your Own Stem Cells Can Treat Heart Disease
The largest national stem cell study for heart disease showed the first evidence that transplanting a potent form of adult stem cells into the heart muscle of subjects with severe angina results in less pain and an improved ability to walk. The transplant subjects also experienced fewer deaths than those who didn't receive stem cells.
Is hepatic differentiation of embryonic stem cells induced by valproic acid and cytokines?
Embryonic stem (ES) cells, known for their capacity to proliferate indefinitely and differentiate into almost all types of cells including hepatocytes, have raised the hope of cellular replacement therapy for liver failure.
Paradoxical protein might prevent cancer
One difficulty with fighting cancer cells is that they are similar in many respects to the body's stem cells. By focusing on the differences, researchers at Karolinska Institutet have found a new way of tackling colon cancer. The study is presented in the prestigious journal Cell.
U of M researchers find 2 units of umbilical cord blood reduce risk of leukemia recurrence
A new study from the Masonic Cancer Center, University of Minnesota shows that patients who have acute leukemia and are transplanted with two units of umbilical cord blood (UCB) have significantly reduced risk of the disease returning.
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