What is Epidermolysis Bullosa?
Epidermolysis Bullosa is a genetic skin blistering condition that affects over 500,000 people around the world, but very few people have heard of it. Those who have realise what a devastating impact it has on sufferers and their families. It is unrelenting in its pain and unrelenting in the distress it causes.
Why haven’t you heard of it?
Because there is no treatment and no cure and as a relatively rare condition it has been easy to ignore.
Groundbreaking research is on the point of delivering treatments and possibly a cure. The work to get there will help people with many other genetic conditions.
For more information about EB click a heading below.
Essential EB facts
EB results from a genetic mutation in one of the genes that have been found to cause the disorder.
There are four main types – Simplex/Junctional/Dystrophic/Kindler
Milder forms of EB cause extensive pain and blistering but do not disfigure and are not lethal.
Severe forms cause death in the first few months of life (Herlitz Junctional) or mitten deformities, extensive skin loss (like burns), anaemia, difficulty swallowing, microstomia (small mouth opening), corneal scarring (sometimes blindness), malnourishment, and eventual death from skin cancer usually between the ages of 20-30 years.
Constant pain. With open wounds like burns all over the body sufferers never have a moments rest from pain.
What research is going to help?
These are looking at :
1) Stem cell
2) Gene Therapy
We are awaiting :
3) Protein therapy trial
4) Drug therapy trial
Research in the UK and US funded by the Sohana Research Fund
100% OF YOUR DONATIONS GO TO RESEARCH
We are proud of this fact.
(John McGrath, KCL,London) a phase l/ll Clinical Trial of Mesenchymal Stromal Cells(MSC) in RDEB
To develop TALEN gene-correction
technology re individualised stem-cell therapy options for children with RDEB (Jakub Tolar,
(John McGrath, London) Understanding how allogenic Mesenchymal stromal cells
can modify disease severity in RDEB
Limbal stem-cell therapy
for RDEB (Jakub Tolar, Minnesota)
Institute of Child Health London
(Qasim) Centrifuge for Gene therapy
LENTICOL-F Gene modified autologous fibroblasts
for local treatment in RDEB
Current debra UK funded projects
McLean/Heagerty 1 (Dundee/Solihull) – To be in a position to move to clinical trials of siRNA on EB Simplex
Bauer 5 (Austria, Italy, Germany) – To develop therapies which combine ex vivo gene therapy with stem cell transplantation for Junctional EB http://www.debra-international.org/research/funded-research-projects/bauer-5.html
Mellerio 1 (London) – To document a Natural History of EB and
validate Clinical Endpoints appropriate to therapy evaluation by industry and regulatory authorities
Gaggioli 2 (Nice, France) – To validate findings that will develop a drug
to counteract scarring and Squamous Cell Carcinoma in patients with Recessive Dystrophic EB
Roopenian 2 (Maine, USA) – To identify modifier genes in Junctional
EB that affect the severity of symptoms experienced by different patients with the same primary gene defect
Brunton 1 (Edinburgh) – Defining the role of Kindlin1 in the regulation of microtubule stability and mitosis
Inman-South 1 (Dundee) – TGFβ signalling in RDEB Squamous Cell
Uitto 1 (Philadelphia, USA) – Novel approaches for read-through of nonsense mutations in COL7A1