Cutting-Edge Stem Cell Procedure Helps Sufferers Of Myasthenia Gravis To Breathe Easier
Main Category: Stem Cell ResearchAlso Included In: Bones / Orthopedics; Respiratory / Asthma; Transplants / Organ Donations
Article Date: 11 Oct 2007 - 2:00 PDT
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Patients living with Myasthenia Gravis (MG) may breathe easier thanks to a rare bone marrow transplant procedure performed at The Bone Marrow Transplant Program at University of California, San Diego Medical Center, the only program in the western United States that has attempted this procedure.
Myasthenia Gravis (MG) is a rare neuromuscular autoimmune disease where the body's immune system, which normally protects the body, mistakenly attacks itself. The transmission of nerve impulses to muscles is interrupted, which ultimately prevents the muscles from contracting. Without the proper nerve impulses, muscles that control breathing can't function.
"It's like dying in your own body," said Ewa Carrier, M.D., associate professor of medicine and pediatrics in the UCSD Blood and Marrow Transplant Division at UCSD's School of Medicine. "Eventually, MG patients can't walk, can't breathe, can't swallow. The signal just doesn't go to the muscles."
This new procedure reprograms the patient's stem cells, destroying them with chemotherapy, before re-introducing purified blood-forming stem cells. After the transplant, the modified stem cells build new bone marrow, renewing the immune system with correct signaling, renewing the immune system with cells that don't attack the body.
The Patient
The Myasthenia Gravis Foundation of America estimates only 20 out of 100,000 individuals in the country have been diagnosed with MG. However, MG is considered under-diagnosed and many more are likely affected but do not know it.
Martin Glasser, M.D., is one of the confirmed cases. Every other day for the past three years, he has visited the plasmapheresis clinic at UCSD Medical Center. Plasmapheresis is a procedure much like dialysis which is used to help MG patients feel better for short periods of time. Glasser's disease was progressing, causing weakness in the legs, arms and diaphragm. Plasmapheresis made breathing easier "but it's a very crude way of keeping you alive," said Glasser.
The Procedure
The procedure was conducted by a team consisting of Ewa Carrier, M.D., Arnold Gass, M.D., professor of medicine at Veterans Affairs San Diego Healthcare System, Geoffrey Sheehan, M.D., UCSD professor of neurosciences and myasthenia gravis specialist and David Ward, M.D., UCSD professor of medicine and Apheresis program founder.
According to the International Bone Marrow Transplant Registry (IBMTR) this rare procedure has previously been performed only three times, all at Northwestern University Hospital in Chicago.
In preparing for the transplant, Glasser's native bone marrow was literally obliterated. Most of the T cells in the body were destroyed.
"The theory is that if the T cells are destroyed before introducing new stem cells, the new stem cells will not receive the old message to attack. After the transplant, the modified stem cells build new bone marrow, renewing the immune system," said Carrier.
Glasser's transplant involved harvesting 16 million of his stem cells. These cells were cleaned with a special device resulting in 8 million pure stem cells. Stem cells at this early stage of development have the greatest chance of producing a healthy line of blood cells.
After the transplant, patients must take antibiotics to protect them from infection. They cannot go to crowded places and must follow special diet requirements until the immune system is fully recovered, which takes about three months.
"There's a possibility that there's also some form of tissue repair going on," said Carrier. "For example, Dr. Glasser did not have feeling in his feet before the transplant and now he has feeling in his feet again, possibly indicating that his peripheral polyneuropathy is improving as well."
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Background
The Rebecca and John Moores UCSD Cancer Center is one of only 40 facilities in the country, and the only one in San Diego County, to receive the Comprehensive Cancer Center designation from The National Cancer Institute (NCI).
UCSD Medical Center offers the only Blood and Marrow Transplantation program in the San Diego region that is affiliated with a renowned School of Medicine and accredited by the Foundation for the Accreditation of Hematopoietic Cell Therapy (FACT). This accreditation is the patient's assurance that a BMT program has passed rigorous standards regarding the qualifications and experience of staff, quality management and patient volume.
The UCSD Apheresis Program, founded by David Ward, M.D., F.R.C.P., in 1982, is the only program in North America to receive full accreditation. Now with units at both the Hillcrest hospital and the Moores UCSD Cancer Center, the program treats many different diseases with several different procedures.
Source: Kim Edwards
University of California - San Diego
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MLA
14 Feb. 2012. <http://www.medicalnewstoday.com/releases/85254.php>
APA
http://www.medicalnewstoday.com/releases/85254.php.
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Visitor Opinions In Chronological Order (2)
Promising
posted by Ruth Boone on 2 Nov 2007 at 11:19 amMy daughter has severe MG and this article gives us hope!
hope for myasthenia sufferers
posted by joan on 21 Jan 2012 at 7:52 pmI have generalized and ocular Myasthenis. tOOK YEARS TO DIAGNOSE EVEN WITH CARDINAL SYMPTOMS. i HAVE SERO NEGATIVE . AAi HAVE SEEN AND STILL DO AS i AM REFRACTORY TO MEDS, ETC., I an the living dead. I go dor IVIG every 3 wks and take many meds including STEROIDS for 10 years, etc/. I Must LIE DOWN multiple time a day. Have cane now.. Choke and use Tickit to help. I have 3 other auto immune illnesses now and heart problems. A flat diaphgram makes breating a real challenge. Myasthenia just gets worse. i've gained lots of weight from mds, cannot exercxise or do much. I have about lost all hope and joy is littl. I know I am blessed in so many ways .. But people do not understand and thru all the crisis from MG i've had..medic elaert and all...they do not care. So much more Just pray the stem cell is something I can do and be alive agai. Thank yo Joan
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