NIH Confirms Protocol To Reverse Type 1 Diabetes
FiReaNGeL writes "In 2001, researchers at Massachusetts General Hospital demonstrated the efficacy of a protocol to reverse type 1 diabetes in diabetic mice. New data from a study performed at the National Institutes of Health provides additional confirmation of the ability to reverse type 1 diabetes and on the role of spleen cells in islet regeneration. Spleen cells appear to contribute to islet recovery more in mice who are older and with more advanced diabetes compared with younger mice with less advanced diabetes, in which regeneration of remaining islets may be the dominant mechanism."
Current investigation, however (both embryonic and adult stem cells), is still in the preliminary stage and several more years remain before they can potentially be used in the clinical setting. Procedures that reduce in vitro manipulation of cells and allow stem cells to develop into islets in vivo are crucial. Furthermore, the regeneration of existing islets is a distinct possibility. Simplistically, it might be hypothesized that down-regulation of autoimmunity may give the pancreas the breathing space to regenerate islets.
It's time to realise that Abble's products are the biggest abomination these days. Just say NO to the dumb iAbble way!!
it will be years before this is available to humans!
I must be missing something ... if the technique was first described and shown in 2001, then reaffirmed in 2003, why haven't they moved forward with trying to treat humans with severe/end-stage diabetes? In fact, they don't even discuss the possibility, which makes me wonder if there is something else in play (bad side effects for example). This sounds like a MAJOR medical breakthrough, and typically breakthroughs like this are pushed into more expanded trials and even human tests faster than the researchers at MGH are moving forward.
Crack - Free with every butt and set of boobs
Who cares about NIH - does Netcraft confirm it?
Uh, gee, could we make sure we have it right first? This isn't a light switch that they are flipping here. We are trudging about in areas that we don't understand yet. They are still making guesses about the mechanism by which it works!
In 2001 one researcher managed to come up with a repair in mice and published. Then other scientists couldn't repeat the findings. Now a few years later we have scientists who can repeat the findings. Sounds like it is progressing very well and at a pace that you would expect it to progress at.
Master - Grasshopper, you must learn patience...
student - Yeah,yeah,yeah... How long does that take?
It's all that damn FDA's fault. We should just abolish it, then the drug companies can make the big bucks selling experimental treatments to try on your two month old daughter. After all, why should the drug companies have to pay for research or prove that it works, when all they have to do is tell people that their new treatment will cure them and they'll line up for the privilege of being a guinea pig.
Of course, for a Type I diabetes thing, they'd be a little bit more careful, after all, if you go around killing children the parents might get a little upset. They'll have to be sure to set up a proper shell company that can be sued out of existence without losing too much money.
It gets me sometimes when comments I see in medical threads are just plain ignorant. Yes, this is only in stage 1 trials. Still, promising results *are* the therapies of the future, and they are relevant and interesting. They are especially relevant when speaking of treating something so widespread and degenerative as diabetes. This already has been an age of miracles, folks. Enjoy what the next 10 years will bring.
An article about this was published in may in the nytimes
However, the TCO is cheaper if you just go to the pet store and buy another mouse.
God I wish I was a mouse... they know how to treat everything for them. Wait... what are you doing? What's in that needle??? NOOOOOOOOOOOOOOOOoooooooooooooooo!!!!!!!
It is very important to note that this is a treatment for reversing Type I diabetes, not Type II.
Type I diabetes comes from an autoimmune reaction against the insulin-producing cells. It is more common in children, and accounts for about 10% of all insulin cases.
Type II diabetes tends to be caused by an insulin insensitivity - the insulin receptor in cells looses its effectiveness. The complications from Type II diabetes tend to be worse, and none of them are pleasant. There are many risk factors for Type II diabetes, some of which a person can't do anything about (i.e., genetic predisposition), but the primary risk factor is obesity and inactivity. So, for the foreseeable future, doctors will no doubt continue to caution people to be vigilant about their weight and, for those under treatment for diabetes, to still be especially vigilant about monitoring their blood sugar levels.
but i think we can all agree, it was worth the wait
I'm a rabbit startled by the headlights of life
http://en.wikipedia.org/wiki/Edmonton_protocol
Although the Edmonton protocol was concerned with transplanting pancreatic islets. I wonder if these two procedures could be combined to give a permanent solution to Diabetes.
Did you ever consider that there are cases with some disease processes where people might be very pleased to consider becoming a "guinea pig"?
Not everyone thinks the government should be their mommy. If you need a mommy, then by all means, have some old lady adopt you. For those adults capable of making informed decisions for themselves, why not stay the heck out of their lives? I know, it is just such a radical idea, but even so... adults, making decisions about their own bodies, for themselves... it almost sounds like... liberty.
But we can't have that. That would be... un-American.
I've fallen off your lawn, and I can't get up.
Thank you science for making it possible to reverse diabetes type 1.
thank you god for giving us diabetes.
They're using their grammar skills there.
True that Type II is probably what most adults have to fear getting.
.. because with it, you require multiple daily injections. The treatment for Type II is usually only pills or inhaled insulin.
However, Type I is MUCH WORSE
http://en.wikipedia.org/wiki/Diabetes
Then other scientists couldn't repeat the findings.
Which other scientists (just curious)? What's suspicious about all this is that JRDF, which will throw money at everything from new implantable device research to stem cell research won't fund research into Denise Faustman's legitimate breakthrough discovery. Could it be because her discovery involve a cheap drug whose patent has expired?
"We are all geniuses when we dream"
- E.M. Cioran
The method reported in Islet Recovery and Reversal of Murine Type 1 Diabetes in the Absence of Any Infused Spleen Cell Contribution may work but at what cost. It requires immune system suppressing drugs and cells from a foreign donor. I suspect that immunoconjugates that prevent the attack of islet cells will be used in conjunction with adult stem cells from the diabetic individual that have been differentiated into the appropriate replacement tissue.
making informed decisions
Informed? Ha!
Take Vioxx. Certain employees of Merck decided that they could simply hide the fact that taking Vioxx was linked with a higher incidence of cardiovascular events. Sure, they could have added that to the documentation on the drug, but then they'd have lost millions of dollars from doctors adjusting doses and moving at-risk patients away from it. They wouldn't have even had to stop selling it, there are plenty of drugs more dangerous than that on the market now.
Tell you what, I'll agree that the FDA can go, when we start charging the employees of drug companies with crimes for their parts in their misinformation campaigns. Manslaughter has a nice ring to it, but it implies "accidental". The execs knew about the risk in the 90's, I believe in most jurisdictions, premeditation is usually grounds for first degree murder.
The fact that there are risks and unknowns do not in any way reduce your ability to make an informed choice. An intelligent adult understands that there are risks and unknowns. You can't be protected from everything, including people who might not care about your particular situation or outcome.
None of that serves as "good reason" to take the right to choose from adults.
As for your outlook on drug companies, fine, whatever. You're entitled to your outlook. That still doesn't give you the right to tell me what to do with my own body.
I've fallen off your lawn, and I can't get up.
Calm down people. They haven't cured diabetes; in fact, this cure for diabetes (in mice) isn't new at all. This isn't a phase I clinical trial. They haven't tried it on people, and I really doubt the FDA will approve any such trials in the next few years.
The controversy is over the role of stem cells. No one disputes that adding Freund's adjuvant to the NOD mice can cure their diabetes, and it seems to work through a hazily-understood modulation of the immune system. That has been established for 15 years. The question is whether adding spleen stem cells to the adjuvant facilitates the process.
When Faustman first published the paper stating the spleen cells were crucial, the NIH quietly contracted three independent labs to confirm the result. No one could could show that the transplanted spleen cells were actually doing anything. Now, it seems that Faustman's group has responded to some of the criticisms, repeated the experiments, and can reproduce their own data. But as long as another lab cannot reproduce it, the role of stem cells will remain very controversial.
Why hasn't there been more of a push to use this in people? The problem in people is that you have to inject the adjuvant fairly early in the disease, and most people with type I diabetes are diagnosed pretty late when most of their beta cells have died. Additionally, no one really knows how exactly the adjuvant works (it's just a bunch of dead bacteria) and whether it will elicit nasty reactions in people that are worse than diabetes itself.
For those technical, you can read the actual papers for free online.
I am posting this anonymously because Denise Faustman has been known to try and sue individuals who speak against her work. In short, I have read the technical comment and the portion that 'reproduces' the earlier work is clearly attributed to Kodama AND NOT NIH researchers. Now why is this important? Kodama is the same person who did the original experiments (in 2001 and 2003) that nobody has been able to reproduce (there have been multiple attempts published, not one has been able to coax MHC mismatched spleen cells as being accepted let alone transdiferentiation into insulin producing cells). So, if this has been around for 5 years now and only one guy in the world is able to do it, something just doesn't sound right to me.
The JDRF is run by parents of children with diabetes, not the pharmaceutical industry. What is more suspicious is that the scientist who supposedly reproduced this work, Kodama, happens to be the same one who did the original work. He has just changed labs. Maybe this is why the JDRF is not funding this work. It has yet to be shown to work by anyone other than the original authors.
Actually, this has yet to be reproduced by another researcher. Kodama did the original experiments and the current ones as well. I would love to see another group be able to reproduce this work but despite the press release to the contrary, it is yet to happen.
We're talking about advertizers here, making provably false claims. Yes, I want the government to prevent companies with good advertizing from killing people.
Please, for the good of Humanity, vote Obama.
The fact that there are risks and unknowns do not in any way reduce your ability to make an informed choice.
That statement is ridiculous on the face of it. How many unknowns must there be before "informed choice" simply becomes "choice"? By your standards, taking a random person and asking him to choose the number you are thinking of would be asking for an informed choice, after all, you told him it's a number and you're allegedly thinking of it. Would a response to the demand of "Answer?" to a person be "informed", since you let the participant know you were expecting one?
In this case, it was a known risk that was known to one participant and not the other. You're welcome to believe that this is "ok", but please find some other name for your abomination of an economic theory, since Capitalism is already taken and in most of its forms requires perfect knowledge sharing as well as rational participants who are not trying to kill each other.
1) Type I Diabetes patients have equally nasty problems (I know of at least two Type I patients...)- some of which are the same
as the Type II patients.
2) Fixing this one would be amazing- it was thought that generally Type I was treatable only with Insulin injections. To be "cured" would be amazing for them.
3) Some of the meds for Type II Diabetes can QUICKLY and VIOLENTLY turn you into a Type I Diabetic if you get exposed to certain other substances. The Avandia type meds and Glyburide type meds that affect utilization and production of Insulin can torch off what's left of the Islet cells in the Pancreas with exposure to things like...oh...alcohol...contrast dyes...handful of other things... When I was taking Avandia and when I was still taking Glyburide I had a list of things that were JUST NOT A VERY GOOD IDEA FOR ME TO TAKE/DO .
4) They have a metabolic switch that they've discovered that turns OFF Type II Diabetes like a light-switch; but you have to take the med for the rest of your life and they're being VERY cautious moving forward with it because it's a genetic based therapy like the Immune System Booster that they screwed up the lives of those poor bastards in the UK earlier this year.
If you've not figured it out by now, I'm a Type II Diabetic. So what if it doesn't help me? It's a fix for the other people out there that don't have the same set of problems I do, but still have serious issues with Sugar- this could free them from every bit of the issues with Insulin shots and needing to manage or avoid sugars. Not everything sugar free is good for you or a diabetic, contrary to the popular belief otherwise- and not everything uses Splenda (nor is it a certainty that it's any better than Nutrasweet, safety-wise...). To not have to worry much ever again... Wow...
I am not merely a "consumer" or a "taxpayer". I am a Citizen of the State of Texas
As the parent of a child with Type 1 diabetes...It is "NOT easy to manage by any means". The technology has made it better but thats where it ends. Try to go to bed wondering if you child is going to be OK in the morning or wonder how his blood glocose is affecting him daily no matter how well you think its being "managed". Your an uneducated idiot...Try to tell your kid that he cannot have a simple glass of orange juice in the morning or anytime of day for that matter, or have to stop him in the middle of playing some activity to check his glucose levels, as they are shaking/trembing telling you he feels fine when its apparent that he is not. My wife and I have not had a solid nights sleep since he was diagnosed at just before his second bithday (nice gift) he is now five. I could go on and on (seizures, coma, shock) "NOT SO EASY TO MANAGE"...Sports teams are managed not diseases.....and most importantly .... Hate to say this but there is no money in finding a cure...there will never be any cure so long as there is money to be made. The pharmaceutical companies in the US are too powerful. Take a moment and think about this it if you are educated enough you will know this to be true. Think about the all the monies raised over the years for any given disease (billions per year do some research but I warn you it gets ugly seeing how much money is raised with very little or no improvements whatsoever)...have they found one cure for anything? the answer is NO...the only chance anyone has in finding a cure lies with stem cells and we all know where thats going...nowhere fast...unless you live in Europe leaps and bounds being made in the are of stem cell research (and please don't post a reply telling me to move that would be stupid and show your lack of any education).
The current nomenclature is type 1 and type 2. Roman numerals are out of favor to describe the kinds of diabetes. The recommendation from the American Diabetes Association came out in 1997. See here.
Great. I knew I shouldn't have had my spleen removed!
I'm 19 years old and have had Type I Diabetes since I was 6.
I don't know what's hurt me more over the years... the pain of growing up diabetic or the pain of watching my parents watch me grow up diabetic. They pushed me very hard to keep myself as healthy as possible. I've always been on a strict diet, tested my blood sugar four times a day, taken four or five shots a day, and have managed to keep my A1C below 7.0 (except for once after I moved away from home when it jumped to 7.2). Despite my years of hard work, I've recently started developing peripheral neuropathy in my left foot. My doctor says it's probably because I'm so tall (6'5") that the nerves going from my brain to my feet are so long that it made them very prone to developing the condition.
Sometimes my foot almost feels normal. Sometimes it just tingles a little. And other times it hurts so much that I can't fall asleep at night. But neuropathy rarely stops at a foot. I may develop cardiovascular, gastrointestinal, or ocular neuropathy some time in the near future. Then it will shift from being yet another burden, to being life threatening.
Fortunately (or perhaps unfortunately), I probably won't have to go through the horrible experience of advanced neuropathy or blindness since I have other medical problems that will probably kill me before I get to any of that or before anyone develops a cure for diabetes that works on humans. I just felt like sharing a small portion of my personal experience. Hopefully this will change the perspective for a few ignorant people out there who think managing diabetes is as easy as popping a few pills that fix everything. Diabetes is a losing battle. Some people fight hard and live long lives. Some don't fight at all and get their limbs hacked off. And some fight and lose anyways.
For the sake of all the other diabetics out there, I hope they really do find a cure soon.
No. It isn't. Risks and unknowns become a problem only when you are thinking they don't exist. If you can see enough of a problem to evaluate it in your own life, then you should be free to do so. Problems and solutions are not evaluated on unknowns, they are evaluated on knowns. For instance, when you take an aspirin, there is an unknown chance that you will exhibit a side effect. You assume it is small (because the odds are small) but that may not be the case for you.
You are who the founding fathers feared; that person who presumes he can dictate actions to others based upon what he thinks is benevolence, when it is really dictatorial evil.
But not to worry. You're in control. Goodnight, mommy.
I've fallen off your lawn, and I can't get up.
Thank You.
I couldn't have said it better myself, and I *AM* a Type 1.
Spent the first 25 years of my life cycling daily, running, hiking, eating healthy foods & generally being as "healthy" as I knew how.
Suddenly I start to get sick, and the next thing I know, I've got "Adult Onset" (26yo) "Juvenile Diabetes" (insulin dependancy) which was found out after I woke up from a week long DKA coma.
With my BSL's in the 800+ range & pH at 6.72, another five minutes in traffic getting me to the hospital and they wouldn't have bothered trying to revive my corspe.
Anyone who tries to tell me that Diabetes is "my fault", risks getting a 50cc insulin injection to the face.
Ok, not really, but it REALLY pisses me off to have someone tell me that my CURRENT weight problem is the CAUSE of my being Diabetic, when it's the complete OTHER way 'round. Then when they try to tell me to "just deal with it", it pisses me off to the point of wanting to SHOW them EXACTLY what it feels like to go through a hypoglycemic reaction despite doing everything possible to keep it at bay.
Diabetes sucks.
My Uncle died of it after losing his legs, an arm, and his vision.
I am NOT looking forward to "old age", which at this point, means hitting 40.
=(
CBC's "Quirks & Quarks" Science program announced the Subject protocol long ago,
;-)
and there have been human trials in subsequent years, in Canada, USA & Sweden,
among other places on the planet.
One problems was that folks who'd undergone the procedure had to take drug to
inhibit their immune systems, ie, to reduce the risk of rejection of the islets.
Nevertheless, some found that acceptable (presumably such drugs could be taken
orally, rather than intravenously).
Any, if I've got the name of the protocol right, up there in the Subject, then
WHY didn't it appear in the post's title?
Giving credit to those who've done the original work is to be expected, even if
that work was done outside the USA.
Still, delays in getting this work translated into procedures available for the
folks who have Type 1 diabetes might well be explained as much in the profitability
of older techniques, both to makes of pumps & doctors.
I'm reminded of the awful metal braces that were -once- applied to the legs of very young
sufferers of polio, ie, in -recent- "dark ages" of the treatment of that disease,
while far less intrusive treatments enabled victims to walk on their own were both
known and practiced by innovative doctors - who had been ignored or insulted, ie,
until their methods were - at last - embraced by the medical community.
"Give me Evidence-Based medicine... or NUTHIN'"
What is more suspicious is that the scientist who supposedly reproduced this work, Kodama, happens to be the same one who did the original work. He has just changed labs. Maybe this is why the JDRF is not funding this work. It has yet to be shown to work by anyone other than the original authors.
Didn't Faustman do the work in this and the original studies? It seem odd that nobody else has tried to reproduce such promising research.
"We are all geniuses when we dream"
- E.M. Cioran
Coincidence?
Either it's Splenda, Saccharin, or not at all...things like Xylitol, Malitol, etc., while they're naturally
occurring sugar alcohols and sweeten nicely, they have a nasty side effect of causing laxative effects past a
certain level of consumption. So, they don't use it as a sweetener at restaurants, in sodas, etc. The only
places I've seen these useful sweeteners is in gums and candies- and not all that often (Seems Aspartame's
VERY popular compared to the alternatives, even though it doesn't taste as good because it's cheap compared
to the allowed alternatives and keeps forever as long as you keep it cool before using it.).
You can't patent a plant, so the FDA won't do what needs to be done for Stevia, which as far as I can tell works
just fine and is as sweet as Splenda happens to be- but as you put it, the big pharma companies (who gave us
saccharin (which was just fine...the studies were so screwed up that it was hillarious...), Aspartame, Acesulfame,
and now Sucralose...) don't want it because they can't gouge for the Patent royalties for the stuff. Sounds
paranoid, I know- but go reading between the lines and it isn't so paranoid.
What they don't tell you about Sucralose is that it's chemical formula means that it's not really derived from
sucrose completely like they tell you it is- not to mention truly chlorinated sugar is more a pesticide and is
rather toxic to humans. It MIGHT be safer than Aspartame, it might not be- but for me, I'm stuck between a rock
and a hard place because of all the stupidity.
I am not merely a "consumer" or a "taxpayer". I am a Citizen of the State of Texas
If you can see enough of a problem to evaluate it in your own life, then you should be free to do so.
What percentage of the population do you think can actually think for themselves? Granted that letting everyone make decisions like this would thin out the gene pool but do you really think that people even read the information sheets that are included with prescriptions? Can we even think that the doctors or the pharmacist would read or care to share the information with the patient if they weren't required by law.
For instance, when you take an aspirin, there is an unknown chance that you will exhibit a side effect.
The usage of aspirin has had a lot of research on it and most people probably know the side effects already. If they don't, they are listed on the box & bottle as required by law. The FDA considers the side effects to be minimal enough that aspirin is available OTC.
Society has developed to the levels we have today by allowing people to specialize. If you require every person in the world to have the ability to understand the complexity of medicines, the world wouldn't have time for everything else.
Jim
[stares hard at Jim, begins to count... 0... moves to next citizen... 1...]
Law for the least common denominator is not a solution. It is a problem.
I've fallen off your lawn, and I can't get up.