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Stem Cells Cure Blindness
The Controversy
Earlier this November, scientists from the University College London Institutes of Ophthalmology and Child Health and Moorfields Eye Hospital were able to restore vision to blind lab mice. This scientific breakthrough signifies that millions of people with optical conditions such as macular degeneration (loss of sight experienced by the elderly), diabetic retinopathy, and a variety of other forms of blindness could be able to regain sight through a remarkably simple procedure. However, the fact that the procedure requires stem cells from foetuses—currently viewed as a highly controversial method by many politicians—has prevented this procedure from becoming more publicized in the U.S. (1).
The Breakthrough
Researchers have identified certain cells on the margin of adult retinas that are similar to stem cells. Additionally, retinal cell replacement may be the most effective method of "cell transplant therapy because photoreceptor loss initially leaves the rest of the wiring to the brain intact” (1). In other words, major surgical reconstruction is not necessary. Any surgical procedure would only involve the superficial layer of the retina and not the particularly sensitive optic nerve wiring at the back of the eye. However, in order to attain human retinal cells at the necessary stage of development, stem cells would need to be extracted from a foetus during the second trimester of pregnancy (1). Because stem cells are able to proliferate and develop into many other types of cells within the human body, they can be extracted from any part of the foetus. However, the timing is imperative if the procedure is to work.
Three Blind Mice… See How the Procedure Works...
1. Early stage retinal stem cells were extracted from a 3 to 5 day old newborn mouse (1).
2. The retinal cells were transplanted onto the retinal surface of a blind mouse whose condition was genetically programmed to resemble the gradual loss of sight characteristic to the human disease retinitis pigmentosa or age-related macular degeneration (1).
3. The cells embed themselves and connected with other cells on the retina of blind mouse. Within 30 minutes the photoreceptors from the retinal stem cells implanted themselves and fused electrical connections with the animals' existing retinal nerve cells (3). As a result, the formerly blind mice's pupils began to respond to light and there was activity in the optic nerve (indicating that the eye was transmitting signals to the brain) (1).
Anatomy & Physiology of the Eye: Photoreceptors
The retina (around 0.5 mm thick) lines the back of the eye. It is lined with a network vascular blood vessels and neurons that gradually channel towards the optic nerve which contains the ganglion cell axons that connect the ganglion cells to the brain. The ganglion cells—the neurons of the retina that transmit images to the brain—are located in the innermost region of the retina and extend toward the lens, or anterior portion of the eye (2). The photoreceptors—the rod and cone shaped cells—are situated toward the outermost portion of the retina and are closer to the back of the eye (5). As a result, light must penetrate the nerve cells within the retina before reaching and activating the rods and cones. Once reached, the rods and cones absorb photons through their visual pigments and translate the photons into a biochemical message and then into an electrical message that stimulates all of the succeeding neurons of the retina. Consequently, “the retinal message concerning the photic input and some preliminary organization of the visual image into several forms of sensation are transmitted to the brain [by] the spiking discharge pattern of the ganglion cells” (2). From then on the brain is responsible for identifying, processing and interpreting the visual image (2).
Candidates for retinal cell replacement surgery must have some retinal cone and rod photoreceptors intact (1) . The retinal cell replacement surgery primarily serves to repair the nerve synapses in the retina, the macula lutea, and the fovea. The surgery cannot generate new photoreceptors.
The surgery mainly repairs the macula and the fovea. The macula functions as a short wavelength filter while the fovea, characterized by a dark circular area towards the back of the eye, is considered to be the most vital portion of the retina. Like the lens, it functions as “a protective mechanisms for avoiding bright light and especially ultraviolet irradiation damage” (2). The fovea is entirely composed of a mosaic cone photoreceptors that are arranged in a hexagonal structure. Outside of the foveal pit, the density of cone photoreceptors becomes increasingly more balanced with that of rod photoreceptors. There is a peak in the density of rod photoreceptors at about 4.5mm (or 18 degrees) from the foveal pit where the rod photoreceptors arrange themselves in a ring around the fovea (5). (Naturally, the optic nerve (the blindspot) is entirely free of photoreceptors) (5). If the macula or fovea cones are damaged (as happens gradually over many years), instant blindness results (2). However, macular degeneration could be easily remedied since stem cells take only about half an hour to develop into photoreceptors.
Repairing the Cornea
In August of 2003, Mike May, a Californian man who had been left blind for 40 years as the result of an accident that happened when he was three years old had his vision restored. Though the vision in his left eye was permanently lost, he could still sense light with his right eye. Researchers implanted corneal and limbal stem cells into his right eye. Five months after the surgery, May was able to sense movements and recognize simple shapes. After two years, he was able to see forms, color, and motion nearly accurately. His 3D perception and face and object recognition remained impaired, though his ability to sense motion was the best restored visual faculty (4).
Like photoreceptors, the cornea is responsible for channelling light through the eye's surface. The corneal surface refracts to provide 2/3 of the eye's focusing power. he corneal surface is entirely transparent and not lined with blood vessels, so the uniformity of cells may contribute to its ability to regenerate more rapidly than other cells in the human body. On the other hand, it is extremely sensitive. There are more nerve endings on the cornea than anywhere else on the human body (6). The cells that compose the layers of the cornea are found to regenerate at a rapid pace, though less rapid than photoreceptor cells. Again, a simple surgical procedure, most of which is processed by human mechanisms, could restore sight to millions of people if only the procedure were to be legalized.
courtesy of U.S. National Library of Medicine
(1) "Cell transplants 'restore sight.'" BBC International News Online. (http://news.bbc.co.uk/2/hi/health/6120664.stm)
(2) Simple Anatomy of the Retina. (http://webvision.med.utah.edu/sretina.html)
(3) "Cell Transplants Restore Vision in Mice." Live Science. (http://www.livescience.com/healthday/535968.html)
(4) "Cell Transplant Restores Vision." BBC International News Online. (http://news.bbc.co.uk/2/hi/health/3171993.stm)
(5) Photoreceptors. (http://webvision.med.utah.edu/photo1.html)
(6) "Cornea." Eye Anatomy. (http://www.stlukeseye.com/anatomy/Cornea.asp)
Comments
ROD CONE DYSTROPHY
Please can anyone elaborate on this and provide information regards STEM CELL THERAPY.This is for my 6yr old son who was apparantly born with the condition.
Await a reply with great anticipation.
siraz.
wondering
i have a 6 and 5 year old that were diagosed with rod-cone dystrophy and i was wondering if there is anything new that would restore their sight. my 5 year old is legally blind as of now. if u could email me and let me know if there is anything that can be done. thanks beth
Loss of vision while in a coma
To whomever can help,
My friend, Rick, lost his eyesight, while in a coma for 2 months, due to a fire accident. His ophthalmologist told him that his blindness wasn't caused by the fire and requested an MRI. The MRI results said his optical nerves are damaged due to lack of oxygen. He is completely blind in his left eye and has 20/200 vision in his right. Is there any possible way to reverse his condition?
MY FATHER HAS LOST HIS SIGHT
MY FATHER HAS LOST HIS SIGHT FOR LAST THREE YEARS,HE WAS SUFFRING FROM GLICOMA SINCE HIS CHILD HOOD. HE IS 65 YEARS OLD.WE HERD ABOUT STEM CEL THERAPY .PLEASE SEND ADRESS OF HOSPITALS OR CLINC THAT START THIS PROCEDURE.I HERD RECENTLY THAT IN CHINA THERE IS CLINIC START ALREADY THIS PROCEDURE.THANK YOU AND GOD BLESS YOU.
MONA SABER SAUDIA ARABIA
Blindness caused by retinal detachments
Can stem cell therapy help regenerate retina's that have been damaged by recurrent detachments? There is a strong family history of retinal detachments and was wandering if this was possible?
retinal detachments
I also have lost considerable sight in left eye due to retinal detachments and surgeries for glaucoma. Please let me know any responses you receive as I am searching for sight help as well.
Optic nerve damage possibly cured by stem cell research
I lost my significant other on 12/15/08 to a heart attack. He'd been blind since open heart surgery in 2003 that damaged his optic nerve; he was 67. I'd like to know where I can make a small contribution in his memory so others don't have to face the heck that he had to the past few years. Doctors told family he'd had stroke that caused blindness. His opthalmologist has kept us informed of research on optic nerve damage since '04; he just recently sent us the data on the stem cell research done with mice. Thanx for your help. Kathy Bem-Elkins
My 19 yr old son has gone blind
I have so many questions regarding this. This all began in February of 2008. He gradually saw blurry vision from time to time and then experienced some dizzyness when standing up. We have been to many Doctors and are now under the care of University of Arkansas for Medical Sciences. We are seriously looking into China and are researching as much of this as possible. He is devastated, he had waited until he was 18 to drive. He was 18 in April of this year and then it was all taken away from him. I am a mother with a pleading heart, and a breaking heart, to see this happen to a good boy which is now a man, this he really is. I pray daily and I must admit as a christian mother I doubted God at first and am still having so many questions as to why. This I guess I'll never know. If anyone out there can offer any suggestions, please help me by e-mailing and letting me know. His optic nerve is completely dead. It wasn't at first but over time has gone pale which means it's dead.
Many Thanks and May God Bless-
Debbie Simmons (Chance Crosland's Mother)
My son was 171/2 when he lost his vision....
Although is was hard to accept my son's blindness, it sure has made my family closer, which I am sure would not have happened if he still had his sight. We spend time together, my son goes to college and his younger brother and him are very close. I am glad that he didn't go into the MARINES, which is what he wanted to do, for so many of our young men have died... I am sadden by his blindness, but I trust GOD knows and see all. I love my son and am looking forward to the day that he may one day see again or as he often tells me, that he will drive, he was able to drive for about a month before his sight was impaired. I am looking to find out about the stem cell procedures and hope that one day they have a cure for his condition.
Optical nerve damage due to lack of oxygen
To whomever can help,
My friend, Rick, lost his eyesight while in a coma for 2 months due to a fire. His ophthalmologist told him that his blindness wasn't caused by the fire and requested an MRI. The MRI results said his optical nerves are damaged due to lack of oxygen. He is completely blind in his left eye and has 20/200 vision in his right. Is there a away to reverse his condition?
Cone Cell Dystrophy
Hi all,
I m Sowmya.My best friend have "Cone cell dystrophy".I really can feel n understand how hard it is.Pls if anyone is aware about any treatment process or informations pls let me know..
Thanks n Regards,
Sowmya
My son has Lebers LHON
My son at 17 was diagnosed with Lebers LHON in January. In a matter of days he lost vision in first one and then the other eye. His vision is now 20/1000 in both eyes but he is attending university and using assistive software and other devices to assist.
My question is if stem cell treatment/therapy will help him with his optic nerve damage. I understand it is difficult but is there hope.Is an optic nerve transplant an option or possible? What clinics and doctors are doing this specific type of research, so that I may follow their work. Please advise and thank you.
hi. I am in the same boat as
hi. I am in the same boat as you. Did you ever find out any answers about stem cell research or an optic nerve transplant??
How is your son doing?
LHON
My Nephew was diagnosed with LHON at 17 as well. My heart goes out to you. He is trying to go to college as well. We are trying to find out options for stem cell therapy. Dr. John Guy has a trial at the University of Florida for LHON.
please help me help my son he has lebers LHON
my son is 15 he was just diagnosed with lebers in march 2009 his centrual vision is gone in both eyes he is know longer in school he is home hospitald (taught at home) .should i put my son on idebenone and vitamin b2 and vitamin c. I was told it worked.idebenone at 45mg 2 to 3 times aday. please email me back if you know anything about lebers you could help me.Thank you
LHON
Katie,
The research in Europe is using 900 mg of idebenone. My son has LHON and it has just gone to his other eye. He is taking idebenone and fish oil pills as well as prespcription eye drops. There is no medical evidence that any of these things work though.
Andy
my family has the LHON gene too..
My nephew who is 18 lost his vision one year ago. Apparently all my sisters carry this gene and we all passed it to our children. We have been doing a lot of research and apparently Dr John Guy at Bascome Palmer is currently doing some gene therapy research. Also Dr Alfred Sadun in California is studing drugs for prevention of the onset of the disease. He is studing a large family who has LHON in Brazil and needs funding to test the drugs. We are in the beginning stages of trying to fundraise for either Dr Sadun or Dr Guy. It is very frustrating that this disease is so under researched and under-funded. Please do what you can to help them find a cure. If we all are proactive and support these drs.... maybe there is a chance we can change the future of our children. I know it is hard in this economic climate.
LHON
My son and I went to Dr. Sadun at Doheny Eye Institue three years ago for experimental treatment. From what we learned, one boy was helped by that treatment, my son wasn't. I am not trying to discourage you. . .it did cost us quite a bit of money since nothing is covered by insurance that is experimental. It was worth a risk, and I would try treatment again if I heard or read anything more encouraging. They were very good to us at Doheny. He helped explain the special challenges with LHON regarding stem cell repair, as well. He also explained what they are trying to learn in Brazil. My son has the 1778 chromosone affect.
We would also be interested in the prevention, of course. One question please, did your son have any asthma symptoms? I am making my own assumptions in regard to this.
Please feel free to write and ask anything.
God be with you all!
LHON
For anyone affected by LHON, please consider joining the two web groups on this topic.
One is a Yahoo message board, at http://groups.yahoo.com/group/LHON_members/
There are a couple of hundred people affected by LHON who regularly share information and ideas.
There is also a Facebook LHON group forming at http://www.facebook.com/group.php?sid=c893ce71f48392cf369a9c4217f2c84e&gid=29805437752&ref=search
There are 130+ member affected by LHON sharing information and ideas about LHON.
I have a son affected by LHON and try to stay connected to the research, etc., and am willing to receive emails at the address below.
We're also striving to raise money for LHON research; see this site: http://web.mac.com/poince/cure
Lissa
LHONpoince@aol.com
lhon
My son was also diagnosed with lhon, mutation 14484c, his vision is 20/300.He is currently seeing a doctor here in LA who deals and talks to other doctors with inhereited eye disesease.There are 2 doctors, one dr john guy in florida and another in france who are doing gene therapy. We also wait for human trials either by gene therapy or stem cell therapy. Please keep in contact.
Looking for help!!
I'm looking to get more information on adult stem cell treatments for type II diabetes for my mother and glaucoma and optic nerve damage for my father. I look forward in hearing back from you as I continue my search for a cure. Thank you.
Steve
MAXIDEX DEXAMETHASONE WARNING
I had eye surgery and in the post-op pack was MAXIDEX(dexamethasone) drops by ALCON LABS.
Two days later I was BLIND
Use Google and enter EPOCRATES MAXIDEX REACTION to verify
Optic Nerve crushed due to car accident
I had a car accident 4 months ago, and due to that i cant see with my left eye. The retina is fine but apparently the optic nerve is crushed. My eye pressure is not stabalizing at all, and it continues to drop to 1. The Drs told me however that the right sides of my optic nerve are in perfect shape. What can i do to improve my eye pressure? any specific diet to follow or vitamins that i need to take to help my Optic nerve? in the future can stem cell help in seeing, even if the sight is not fully restored like before??
Thanks
RI
research
I would like to find out more about opportunities to volunteer for stem cell research for retinitis pigmentosa. Would you please send me more information? I am a 50 year old man who was first diagnosed at the age of 14. I am light sensitive at this time.
Father lost his vision after back surgery
2 years ago my father lost his vision when doctors were doing a back surgery. They told him the cells on his optic nerve died. Is there anyoned else who has heard of this and is their any help for him.
Optic Nerve Hypoplasia
To whom ever can help,
Our son is three months old and was just diagnosed last week with ONH. He will be getting an MRI this coming week, I know that this is our first step. On the other hand, we have of coarse been researching on our own. Everytime we look something up about the cure we are told of China's cures with stem cell surgery. Past this brief information we do not know who to contact to learn more. If anyone has any info on contacting a specialist who can help or even a website with details PLEASE reply. It would be Greatly Apreciated!!!!
Mr and Mrs Freels
It is enlightening to come
It is enlightening to come across this information. My brother had a major car accident in 2000 and as result is visually impaired (totally blind in both eyes) due to damage caused to his optical nerves. Could you please inform me if this procedure can assist him and if you can not answer this without examining him, please let me know where and when so we can make arrangements. I eagerly await your response.
Concerned brother
My daughter is 6 months old
My daughter is 6 months old and we have recently been told by a doctor that she has an undeveloped optic nerve. They told us that there is nothing that can be done. Is there any new procedure? Anything at all?
your child can live a
your child can live a healthy life without the treatment so please dont think its the end of the world i am 17 doing alevels with the condition and would like to find out if it is possible to get a cure so i have the choice if you here anything please tell me
RE: Optic Nerve Hypoplasia
Hi. Have you gotten any info? My son has ONH and I know quite a bit. Please feel free to email me.
Lori
Hi Lori, I have a 5 year old
Hi Lori, I have a 5 year old daughter with ONH. She has severe low vision and is legally blind, she has some sight but its very minimal. I would love your help with any information on this and any treatments available.
Thanks so much,i look forward to hearing from you.
Hayley
ROD-CONE DYSTROPHY
MY FATHER AND I HAVE BOTH BEEN DIAGONOSED WITH ROD-CONE DYSTROPHY. I JUST RECENTLY FOUND THIS ARTICLE AND WAS CURIOUS TO SEE IF THE STEM CELL REASERCH WOULD BE ABLE TO HELP US ONCE IT IS READY TO BE USED ON HUMANS? WE WERE BORN WITH THE DISEASE AND WERE TOLD IT IS HEREDITARY. I HAVE A DAUGHTER WHO IS 5 BUT SHOWS NO SIGN OF HAVING THE PROBLEM. SINCE I'M ONLY 27 I PRAY DAILY FOR A CURE FOR THIS.
THANKS,
INDIANA
Blindness caused by meningitus
My husband got meningitus in october 2007, this caused him to lose his sight.
We have been told that his eyes and optic nerves are healthy but the meningitus has damaged a part of his brain that sends messages to his eyes to enable him to see. He can see shadows of things but cannot see features of things and says everything is grey and wishes that someone could turn a light on to enable his eyes to see again. does anyone know if anything can be done to restore his sight.
meningitis
my brother AT 47YRS OLD last yr came down with bacterial meningitis he was in A COMA FOR 6 DAYS.I LOOK EVERY DAY FOR SOMEONE OR SOMETHING TO HELP HIM.IF I HEAR OF ANYTHING I WILL CONTACT YOU.BEST OF LUCK
stem cell treatment
my daughter lost her eyesight at 9 through a brain tumour that was treated with radiotherapy, which caused stretched damage to her optic nerve.
would stem cell treatment help her, and if so where would she be able to receive treatment?
i would be obliged if you would reply by e-mail as soon as possible.
thank you for your time
left homonomous hemianopsia
I was hit by a car when i was 12 resulting in homonomous hemianopsia on the left side. I am now 30 years old. Is there any hope for my vision being restored?
Foveal hypoplasia, nystagmus and astigmatism
Hello I'm 20 years old and have foveal hypoplasia, nystagmus, astugmatism, and an under developed optic nerve. i have been looking for a way to correct the vision loss I have and had no luck so far. do you think this could help me in some way?
Thanks, Courtney
Nystagmus
I too have nystagmus and astigmatism, have you had any luck in your search? I am 24 years old and the nystagmus gene is in my family, with my lack of vision I am desprate to try anything.
Optic Nerve Injury
I lost my right eye vision in a road accident on Feb/08/2008. The eye doctor said that there is an injury in my optic nerve due to the Zygomatic bone fracture. Please let me know if there is any treatment available.
Thanks,
Jos Collin
Optic nerve hypoplasia
Dear Ma'am or Sir,
My brother is fourteen years old. He was born with Optic Nerve Hypoplasia. My mother and I have searched everywhere for a cure. When she and I heard about this stem cell thing actually working, we were just absolutely floored. If you have any info. what so ever, feel free to e-mail me.
Thank you!!
o.n.h.
hello.my gırl baby 1 old.My, girl, this, desease, be born, please, communication, dry,
mail:fatihcakir4510@hotmail.com
manisa city/turkey
peters anomaly
My 6 year old son was born with Peters Anomaly. He had several corneal transplants but due to complications with glaucoma his retinas detached and he is blind in both eyes. Would any of this be helpful to him?
Im not political....
I have someone in my life that is legally blind and have not been able to stop researching optic nerve regeneration...but from what I am gathering, Pres. Bush put a stop to stem cell research years ago.
I remember Hilary talking about it and just checked out her views at http://www.votehillary.org/CMS/node/737, though I dont follow politics, I am sure going to make my way out and vote for her!!!!! I cant believe that our government is hindering the progress of our health and welfare....its a D*& shame.
Just imagine how much further those wonderful researchers at Harvard, Boston and every where else, can go, and just how much it will expedite what we are all looking for here. An answer to our prayers.
Optic nerve damage caused by pressure
Hello, I have a 2 yr old daugther named Alexis. She is currently blind because of pressure to the optic nerve caused by a tumor. She had neuroblastoma which is a rare childhood cancer. She is doin fine right now. Right now she is undergoing a stem cell transplant would that help her? I would really like some answer. Do you know anything that could help her see again?
I hate looking at my daughter knowing see cant see me!! --- desprite ---
optic nerve damage
Hi
my son lost his vission after motorbike accident. his optic nerve is damaged and he is blind i am desprately trying to find out any medical attention that can bring his vision back.
right homogmous hemianopsia
Hi. My daughter was in a severe car accident with a tramatic brain injury. She has lost vision in the right side of both eyes. Is there anything that can be done to correct or improve the loss vision where she could drive again?
Thanks
blind as a result of crushed optic nerve (accident)
i want to be able to see again and live a normal life. i was in a car acccident about 7 years ago and doctors say the optic nerve in my left eye was crushed. could stem cell help me?
optic nerve damage
iam in the same boat exactly as you are. i was in a major car accident may 08 and doctors believe my optic nerve was damaged during the accident. a cure would be awesome.
Pattern Dystrophy
My 25 year old son has recently been diagnosed with Pattern Dystrophy, and given no hope for treatment. Would stem cell transplant be an option, or is there any other help for his vision.
I have optic nerve atrophy but heard it can be cured in China
I have heard that biekel biotech has a new treatment for optic nerve atrophy throught stem cells. I don't know if it will cure my vision or not and it is a huge price to pay to say if it'll work or not. The total cost is $24,000 USD and that is a lot. Is this a Chinese scam or is this for real? The leading person's name is Krishner but I don't know if I trust it or not. I wanted to get some feedback on it from anybody that knows anything. I have optic atrophy in both eyes and I am legally blind because of it, corrected is 20/200 with glasses. If anybody knows anything or would give me any opinion or suggestion then please don't hesitate to contact me
Thank you