GETTING INVOLVED
Just wanted to know from the more experienced forum members if its possible to get involved in helping those involved in this promising research gain partnerships and donations from organisations such as the ms society? If many of us e-mail them about how excited and hopeful we are about this maybe theyed consider providing some funds.
wow thanks for that link...really encouraging. am a med student also and i've had to litterally put my life on hold for now.Hope this comes thru
I just watched that video and they said it could be ready for humans within 2 years :)
http://montreal.ctv.ca/servlet/an/local/CTVNews/20090812/mtl_090812/20090812/?hub=MontrealHome
Lets hope so!! and also that they get the funding for further research.
Debs
I think by them saying early stages means rrms stage of the disease, before it goes into the progressive stage, so the early stages could be like up to 15-20 years or so before it turns progressive.
When will they start testing this on humans???
ScienceDaily (Aug. 12, 2009) — A new experimental treatment for multiple sclerosis (MS) completely reverses the devastating autoimmune disorder in mice, and might work exactly the same way in humans, say researchers at the Jewish General Hospital Lady Davis Institute for Medical Research and McGill University in Montreal.
MS is an autoimmune disease in which the body's own immune response attacks the central nervous system, almost as if the body had become allergic to itself, leading to progressive physical and cognitive disability.
The new treatment, appropriately named GIFT15, puts MS into remission by suppressing the immune response. This means it might also be effective against other autoimmune disorders like Crohn's disease, lupus and arthritis, the researchers said, and could theoretically also control immune responses in organ transplant patients. Moreover, unlike earlier immune-supppressing therapies which rely on chemical pharamaceuticals, this approach is a personalized form of cellular therapy which utilizes the body's own cells to suppress immunity in a much more targeted way.
GIFT15 was discovered by a team led by Dr. Jacques Galipeau of the JGH Lady Davis Institute and McGill's Faculty of Medicine. The results were published August 9 in the prestigious journal Nature Medicine.
GIFT15 is composed of two proteins, GSM-CSF and interleukin-15, fused together artificially in the lab. Under normal circumstances, the individual proteins usually act to stimulate the immune system, but in their fused form, the equation reverses itself.
"You know those mythical animals that have the head of an eagle and the body of a lion? They're called chimeras. In a lyrical sense, that's what we've created," said Galipeau, a world-renowned expert in cell regeneration affiliated with the Segal Cancer Centre at the Jewish General and McGill's Centre for Translational Research. "GIFT15 is a new protein hormone composed of two distinct proteins, and when they're stuck together they lead to a completely unexpected biological effect."
This effect, explained Galipeau, converts B-cells -- a common form of white blood cell normally involved in immune response -- into powerful immune-suppressive cells. Unlike their better-known cousins, T-cells, naturally-occurring immune-suppressing B-cells are almost unknown in nature and the notion of using them to control immunity is very new.
"GIFT15 can take your normal, run-of-the-mill B-cells and convert them -- in a Superman or Jekyll -Hyde sort of way -- into these super-powerful B-regulatory cells," Galipeau explained. "We can do that in a petri dish. We took normal B-cells from mice, and sprinkled GIFT15 on them, which led to this Jekyll and Hyde effect.
"And when we gave them back intravenously to mice ill with multiple sclerosis, the disease went away."
MS must be caught in its earliest stages, Galipeau cautioned, and clinical studies are needed to test the treatment's efficacy and safety in humans. No significant side-effects showed up in the mice, he said, and the treatment was fully effective with a single dose.
"It's easy to collect B-cells from a patient," he added. "It's just like donating blood. We purify them in the lab, treat them with GIFT15 in a petri dish, and give them back to the patient. That's what we did in mice, and that's what we believe we could do in people. It would be very easy to take the next step, it's just a question of finding the financial resources and partnerships to make this a reality."
Reference to this website: http://www.sciencedaily.com/releases/2009/08/090811143725.htm
Thanks heaps, thats really exciting!!!
xxxx
Sammy
magic bullets take many years of good science, trial and error, lots of work and money -- and mucho luck. certainly a good direction they are proceeding in. may be some other discoveries will come from their efforts to help others.
love the science of it though, fascinating stuff ...
thanks for the link
Experimental Autoimmune Encephalomyelitis is what is being reversed. EAE is a model in mice for the different stages of demylating disease. So far no one can recreate MS in mice it it to complex. This is promising.
Alex
hmmm...i don't know the name but am guessing u're talkin bout the model previous to the just discovered model spoken about here....http://www.sciencedaily.com/releases/2009/06/090610133503.htm
But what they are saying with this new model is the discovery that b lymphcytes play a much more important role than was expected. The reversal i mentioned in my first post involved mainly b cells which are converted into immuno-suppressers by combining 2 proteins. How cool is that...So am still quite hopefull
I'm wondering if they're talking about the EAE model that they use for MS in mice. As far as I know, it's just an MS mimic - it doesn't accurately copy the disease.
Hmmm..you have a good point. Hopefully that ELISHA test i was reading about comes on stream by then. They use antibodies to detect auto antiboidies in ms. Kinda like the ELISA test. Am quite hopefull for MS. Seems to be a lot going in terms of discoveries. I just hope someone funds this research.
Very interesting - but did you catch that they say MS has to be caught in its earliest stages? How on earth do we do that when it doesn't show up easily in any tests in the early stages?
Lulu