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DNA Vaccine May Treat Multiple Sclerosis

GSASoftware writes "Multiple sclerosis is a serious, as-yet incurable neurological disease which causes blindness, paralysis and other serious symptoms. In a new development, a neuroimmunology researcher in Montreal has developed a therapeutic DNA vaccine. The cause of the disease is not fully understood, but it appears to be auto-immune. If a DNA vaccine can be an effective therapy for this auto-immune disease, is it possible that DNA vaccines could treat other auto-immune diseases like Crohn's, eczema, and others?"

127 comments

  1. double entendre by User+956 · · Score: 0, Flamebait

    DNA Vaccine May Treat Multiple Sclerosis

    The best vaccine against unwanted "DNA" is a condom. If it helps against Multiple Sclerosis too, that's fantastic.

    --
    The theory of relativity doesn't work right in Arkansas.
    1. Re:double entendre by timmarhy · · Score: 0, Troll

      No babies come from ass sex either remmeber.

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    2. Re:double entendre by janrinok · · Score: 3, Informative

      Your comment has been tagged as Funny. I hope that is how you intended it to be (and the title suggests that you did), because otherwise you are being totally ignorant and offensive. I have a loved one who is suffering from MS. She hasn't done anything to 'deserve it'. It isn't caused by having loose morals. Its effects, however, are devastating. Her life and my own, as well as the lives of many members of our family, have been changed as a result of the disease. Our home has had to be modified so that she can live on a single level, our plans for the future have been destroyed as she is unable to do the everyday things that we had planned to do, and her daily life is very much affected by the limitations that are brought on by the disease. To her, a visit to the local shops is a difficult adventure, to travel further afield might sometimes be impossible, to sit in the garden and look at the flowers can be the most exciting thing to occur in her day, to do some housework presents her with challenges that you and I cannot imagine. Personally, I find it hard to view such things as 'Funny'. Enjoy your laugh, I will not begrudge you that, but I hope that there is some light at the end of our tunnel as a result of the research that is described in the article.

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    3. Re:double entendre by chuckymonkey · · Score: 1

      That's part of the problem though. Teaching abstinence is all well and good if you live in some kind of dream world where people only have sex after they're married. Humans are sexual creatures, we're hard wired to have sex and we're going to do it since the survival of the species relies on it. As my parents did for me I will do for both of my daughters, education about the safer ways to have sex and the joy as well as the dangers of it. I'm a dad so teaching my girls about sex isn't going to be fun for me, but I would much rather they have a healthy attitude about it and not try to hide it from me than for them to learn about it on their own and end up pregnant or worse. Both my wife and I had sex before we were married with others and with eachother and we're much happier as a result, we knew before we were married that we were compatible sexually and emotionally which has lead to a very long and healthy sex life with no urge on either side to seek sexual satisfaction extramaritally. Anyway, abstinence is a great ideal but it really doesn't have much of a place in reality. Back on topic though this is great news and I hope that it can be refined to bring a lot of light and joy to some people that live a very very difficult life.

      --
      "Some books contain the machinery required to create and sustain universes."-Tycho
    4. Re:double entendre by MemoryDragon · · Score: 1

      I cannot really say it is funny, a friend of mine has this disease, I must say it is one of the most terrible things I have ever seen. What happens is that your physical condition goes gradually down (so does your mental condition to some degrees in the later stages)
      this is endless suffering for decades.

      I am not sure which disease is the worst, but MS is definitely a candidate for worst disease!

    5. Re:double entendre by janrinok · · Score: 0, Offtopic

      I'm not in Germany, nor am I German. But thank you for hiding behind your AC when you haven't got the balls to say it as yourself.

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    6. Re:double entendre by janrinok · · Score: 0, Flamebait

      Another brave AC who hasn't got balls. But I suppose that you think that jokes about other crippling diseases, such as cancer, motor-neurone disease etc, are also funny? It was not a bitch fest - but for those with small brains need to be reminded that what might appear funny to them can be quite painful for others. As I said, I don't begrudge you (or anyone in fact) having a laugh but if you need to hide behind an AC to have a joke at someone else's expense, then perhaps you have already realised that it wasn't as funny as you hoped it would be. I hope that you never suffer from any such illness but, if you do, you will hear my laughter wherever you are....

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    7. Re:double entendre by janrinok · · Score: 1

      Thank you. As you will have noticed from my posts above, I also cannot see a funny side to this. If this had been an article about CPUs, power supplies or YRO, there would have been a serious discussion. As it is, many seem to think that such diseases are simply a cause for jokes. My family do laugh about MS, otherwise we would not get through some days, but we do not laugh at the sufferer but at the disease's effects. Many comments in the posts seem to think it is a sexually transmitted disease - which shows their ignorance - but they are probably unaware of the myriad of symptoms and their effects upon the sufferer.

      I am sceptical of the discovery but hope that there is something useful in it. However, to the best of my knowledge, there is still nothing on the horizon that holds as much promise as this discovery so this is, for the time being, the best chance for many people.

      --
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    8. Re:double entendre by Anonymous Coward · · Score: 0, Interesting

      we knew before we were married that we were compatible sexually and emotionally which has lead to a very long and healthy sex life with no urge on either side to seek sexual satisfaction extramaritally.

      I'm afraid the statistics show otherwise... those who have sex before marriage (especially with other partners) are more likely to get "extramarital" than those who don't. It makes since, you get used to getting different partners, then you get "stuck" with one.

      Abstinence is hands down the best policy, it will stop unwanted pregnancies (and therefore the many convenience abortions) and statistically you will be happier in your marriage.

      Submitted Anonymously to protect my karma from closed-minded /. robots.

    9. Re:double entendre by utopianfiat · · Score: 1

      Oh christ, this is some crap. Tell me exactly how someone can be statistically happier? Before I quote Mark Twain on this one, why do people enjoy basing their life decisions on statistics? Seriously, do people really become abstinent because they feel like it has an 'empirically demonstrated potential to decrease the chances of my unhappiness'? Does anyone besides me realize how absurdly stupid this logic is? How do you even quantify this?
      The biggest problem I find with your post is that it assumes everyone is a monogamist, which isn't true by a long stretch now-a-days. Some singles don't intend to settle down, and don't intend to marry, and this is an increasingly common lifestyle among young adults; possibly, just maybe because we all grew up during the reganist social prohibitionism bullshit that permeates american life to this day.
      Rather than seek a sexually satisfying marriage by eliminating all other options, perhaps the better alternative is to find a marriage that is both sexually and emotionally satisfying; a good choice of a mate, rather than the first nice christian girl/boy that comes along.

      --
      +5, Truth
    10. Re:double entendre by Mister+Whirly · · Score: 1

      Sounds like a total cop-out justification for not being charming enough to get laid. Dude, wash your face more, come out of your parents basement more often, and make an effort to be a little more social to the ladies. It really isn't that hard - you have hormones and instinct working FOR you as stated in the earlier post. The desire to reproduce is one of the most common "hard wired" instincts in all animals. Humans are the only animals stupid enough to try and go against nature by promoting "abstinence". I mean after all, you don't want to slap God in the face by telling him that the urges he instilled in you are wrong, do you?

      --
      "But this one goes to 11!"
    11. Re:double entendre by Hognoxious · · Score: 1

      I'm not in Germany, nor am I German.
      Then you've no excuse for being such a homourless dickhead, have you?
      --
      Confucius say, "Find worm in apple - bad. Find half a worm - worse."
    12. Re:double entendre by Slashdot+Parent · · Score: 1

      My family do laugh about MS I'm not sure how this is possible.

      Like I said before, I considered MS from all angles and failed to find any opening for humor. Not even in the context of a cure having been found and looking back on the challenge of the time.

      It's usually funny to look back at some challenge you faced and see it as humorous. Example: "Remember that time we were in Vietnam and we were looking for... which Wat was it? I don't even remember... anyhow, we got out at the bus station and there was this map of the town, but it lacked a 'you are here' sign and we just wanted to know where we were on the map so that we could orient ourselves. We kept trying to convey to locals through various charades and dances and hand signals our predicament, to no avail. Boy, was that funny."

      Now let's try it with MS: "Remember that time when you went blind in one eye? Except the eye didn't go 100% dark, it instead went 100% bright and if you opened your eye, it was so bright it looked and felt like you were staring into a wall of 1,000 suns. Remember how painful that was? And how you had to wear that patch on your eye for everyone in the world to see and ask how you injured it, and you had to explain it dozens of times despite how badly your head was throbbing? Wasn't that funny?"

      Yeah, not so funny. Lousy stand-up material, for sure.
      --
      They don't grade fathers, but if your daughter's a stripper, you fucked up. --Chris Rock
    13. Re:double entendre by Bastard+of+Subhumani · · Score: 1

      Many comments in the posts seem to think it is a sexually transmitted disease
      In a way it is - as are hemophilia, sickle cell anemia and ginger hair.
      --
      Only three things are certain; death, taxes, and apocryphal quotations - Ben Franklin.
    14. Re:double entendre by janrinok · · Score: 1

      No, there is no proven genetic link. We have gone back 4 generations and there is no trace of MS in the family history. That hardly makes it look a convincing case for a genetic disease. In fact, no-one actually knows yet what causes it. They can see its effects on the body, and they can view the symptoms that people exhibit, but they are still at a loss as to the cause and cure.

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    15. Re:double entendre by janrinok · · Score: 1

      I fully agree, not many aspects of MS have a humorous element. But we have managed to find laughter from time to time. The best jokes are the ones told by the sufferer about the problems they are experiencing. For example, the sufferer's loss of balance can cause an effect similar to that seen in drunken people. In this case, the sufferer made light of the issue by pointing out that we were all drinking beer at a BBQ to achieve a similar effect, so look how much she was saving in both time and money! OK, it is not a joke that can be told to great effect, but we all laughed - including the sufferer - and it made MS seem, for a moment or two, something less frightening to us all. Another example which brought a smile to many faces was when 2 MS sufferers had a wheel chair race to join the queue to buy an ice-cream. It was obvious that they found life difficult but they both enjoyed the short competition and the existing queue, faces full of smiles, stood aside to allow them to be served first. MS is serious business but, from time to time, a little laughter can perhaps be found.

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    16. Re:double entendre by janrinok · · Score: 1

      Ah, such incisive wit! Each word crafted to cause the maximum mirth in the reader. You must be really proud of your contribution to this thread. Your comment has certainly added an invaluable and intelligent insight into the problems that medical science is currently experiencing. Now piss off and let the adults have a discussion.

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    17. Re:double entendre by Bastard+of+Subhumani · · Score: 1

      Change the record, your grumbling about AC's is getting really tedious. Here I am, all logged in - what are you going to do - beat me up after class? Grow the fuck up already.

      --
      Only three things are certain; death, taxes, and apocryphal quotations - Ben Franklin.
    18. Re:double entendre by Bastard+of+Subhumani · · Score: 1

      No, there is no proven genetic link.
      It's not disproven either.

      We have gone back 4 generations and there is no trace of MS in the family history. That hardly makes it look a convincing case for a genetic disease.
      Unless your family is the only one to ever exhibit this disease, that proves nothing. Not really a huge sample size, is it?
      --
      Only three things are certain; death, taxes, and apocryphal quotations - Ben Franklin.
    19. Re:double entendre by janrinok · · Score: 1

      So how do you substantiate your claim that it is a sexually transmitted disease?

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    20. Re:double entendre by Some_Llama · · Score: 1

      "Both my wife and I had sex before we were married with others and with eachother and we're much happier as a result,"

      So you're suggesting the only way to be happy sexually is to be promiscuous? or try each other out before you get married? I have to disagree.. the male and female genitalia go quite well with each other and i don't see anything you could learn in the bedroom about your partner that you wouldn't learn through dating for a number of years...

      2 people who are virgins who get married (and then have sex) after getting to know everything about each other through years of dating would be much much closer than 2 people who fucked a lot and then got hitched... probably more so.

    21. Re:double entendre by PermanentMarker · · Score: 1

      I can asure you, you will learn more from different teachers then from one teacher. Some pretty boys and girls keep going to the same school. While others travel around and learn a bit more.

      It counts for religion to (as thats your problem here). You can believe in a God, but you might learn also from other believes or phylosophies. As besides you where given a dick you where also given brains. And emotions like passion and love

      The best thing you can do is learn from this world
      But before you react on me, see the movie http://www.zeitgeistmovie.com/ It will tell you a lot about origin of believes and who uses their power. Note I'm not against any believe, but i'm strongly against people who are made blind by believe. Those who forget that the world is also a natural peace and nature place, with natural behaviours, and nature to take care of but not to miss use. To find the balance between the nature around you and yourself, isn't easy. But its better to solve that first before you get in some holy guy who will forgive all your blames. As that is too easy. And made us care less for the world around, poisening our earth and has created a lot of wars.

      I give you one eye opener, this word: AxisofEvil
      It means that someone used a a believe system with a god and a devil character.
      To get that believe behind him to be able to start new wars for political (oil) reasons. Since he used this words and no other words for it, he was sure he would get those people behind him. Thats the danger with those of you who exhanged their hart for some kind of book.


      So just follow your hart and sometimes your dick will follow your hart, but its your brain and what you want to learn from this world what decides what happens. You can learn yourself there are no books required as long as you dont hurt others it's all okay to me.

      --
      I know you're out there. I can feel you now. I know that you're afraid. You're afraid of us. You're afraid of change.
    22. Re:double entendre by Hognoxious · · Score: 1

      Now piss off and let the adults have a discussion.
      Why don't you try and make me, faggot-knickers?
      --
      Confucius say, "Find worm in apple - bad. Find half a worm - worse."
    23. Re:double entendre by kaniaro · · Score: 1

      I really hope the STD folks are joking, but on the off chance they're not - if MS is an STD, then so are you. Literally, since you're calling pregnancy an STD.

    24. Re:double entendre by Anonymous Coward · · Score: 0

      Ah, such incisive wit! Each word crafted to cause the maximum mirth in the reader.
      You're not exactly Oscar Wilde yourself, pal.
    25. Re:double entendre by janrinok · · Score: 1

      LOL. But it did take 13 days for the reply....

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  2. Re:Snuh! by dwarfsoft · · Score: 0, Offtopic

    I'd be more worried as to why one would eat a blue dress in the first place...

    --
    Cheers, Chris
  3. Always a possibility by charleylc · · Score: 3, Insightful

    There's always the possibility that it *could* work for other auto-immune diseases.
    It's kind of mute point, though, to ask such a hypothetical question when the original story is about a new therapeutic DNA vaccine that only produces "beneficial changes" with "periods of remission".
    While this is a huge step forward, it is far from being introduced into the mainstream medical community for mass use. TFA states that it is in the early stages of being studied.
    Although the article does say that it's possible that it could be developed for other auto-immune diseases, I think it's a little preemptive to start asking such hypothetical questions when the target disease for which the drug is being developed isn't even out of the test stage.

    1. Re:Always a possibility by dberstein · · Score: 5, Informative

      I suffer from MS; the last I heard of a vaccine was last year: they shut the study after a couple of patients died.

      This is are very interesting and promising news for me. Perhaps in a couple of years I won't need my daily anti-fatigue pills, weekly interferon beta 1a shots, and those occasional hospital corticoid shock treatments. Probably I'll never recover for the disabilities I've already got, but at least I won't develop any further because of MS!

    2. Re:Always a possibility by dberstein · · Score: 1

      Following your logic technically they weren't cured either.

    3. Re:Always a possibility by Anonymous Coward · · Score: 1, Informative

      There is some indication that parasites might help you as well.

      Basically the theory, which originated from the observation that autoimmune diseases were vastly more prevalent in the developed world, goes that there has been a natural selection for parasites that manage to downregulate the immune system (so as to stop it from attacking them). This made a corresponding natural selection for more aggressive human immune systems. Basically you had somewhat of a downregulation aggression race which was pretty balanced. Then, in one generation, the parasites were wiped out, leaving many humans with way too aggressive immune systems.

      Who knows, but it does seem to be quiet a hot research topic (although it is currently mostly focused on the likes of Crohns), with several articles in medical journals and at least two companies into producing worms. Here's a link to some results with respect to MS.

      Good luck with your disease.

    4. Re:Always a possibility by tfoss · · Score: 2, Informative

      It's kind of mute point *putting on grammar/diction nazi hat*
      No, it's a moot point.
      -Ted
      --
      -=-=- Quantum physics - the dreams stuff are made of.
    5. Re:Always a possibility by charleylc · · Score: 1

      Thanks. I realized it AFTER I hit the submit button. I should have previewed first.

    6. Re:Always a possibility by Anonymous Coward · · Score: 0

      Does he? Where?

    7. Re:Always a possibility by mr_matticus · · Score: 1

      Parent is not off-topic. Knowing how to use words when making your case is most certainly relevant information. Using words improperly does a great disservice to an otherwise strong post. Correcting misconceptions (particularly "mute point" which many, many people say) allows people to be taken seriously. If you said this at a symposium or panel, you'd hear giggles throughout the room.

    8. Re:Always a possibility by dmpyron · · Score: 2, Interesting

      I have a friend with MS. She goes in once every 4 weeks for an infusion of Tysabri. It's supposed to be the next miracle. It's prevented the formation of new lesions in over 90% of the test subjects. The previous med was beta interferon, IIRC.

      Tysabri was pulled from the market in 2004 after two of the test subjects suffered from some sort of disorder that "turned their brains to mush" (Sarah's words). A further trial had no adverse results. She's had no new lesions and is currently asymptomatic.

    9. Re:Always a possibility by CommonModeNoise · · Score: 1

      Having MS I follow the research news (see National MS Society website to find listings). The good news is that there are many "promising" treatments, including this one. However the press release descibes the result of a "Phase I" study, which by definition is an experiment to determine the _safety_ of a new treatment, not its efficacy. Most candidate treatments that do OK in their Phase I study, fail in their Phase II and Phase III studies. Only 3(4) drugs have run the gauntlet and are in use for non-experimental treatment (one is available only under special conditions). The role of various cells of the immune system, of myelin destruction and other (unknown) neurodegenerative processes, the cause, and much more are hotly debated in the research literature. Myself, I'm insisting on both a cure AND a method to repair the damage already done. So there!

    10. Re:Always a possibility by gold · · Score: 2, Interesting

      You and others suffering from MS, other autoimmune disorders, or even cancer may wish to research low-dose Naltrexone treatment: http://www.lowdosenaltrexone.org/index.htm and http://en.wikipedia.org/wiki/Low_dose_naltrexone.

    11. Re:Always a possibility by Hognoxious · · Score: 1

      They could have been cured of the first disease, but died of something else. Like if you had a septic earlobe and were decapitated.

      --
      Confucius say, "Find worm in apple - bad. Find half a worm - worse."
    12. Re:Always a possibility by Anonymous Coward · · Score: 0

      Please, for the love of god, it's a "moot" point. All points are mute, but some of them matter.

    13. Re:Always a possibility by NelsChristian · · Score: 1

      You need to watch the 1coyote's progress using the Marshall Protocol against the MP. Dr Marshall has identified the mechanism that various bugs use to defeat the immune system, and also how to stop that. It worked for my sarcoid, and for a number of other auto-immune diseases (diabetes, lupus, etc.). There have been other MP/MS patients, but they don't tend to update their progress on the web site.

    14. Re:Always a possibility by Anonymous Coward · · Score: 0

      Before we get ahead of ourselves, lets be thankful that they are dealing first with this crippling illness MS. There is nothing out there that stops the progression of this ill fated illness. All the conditions you mention do not affect one's potential to walk, stand, etc. just an example. Next I hope its ALS.

  4. Well, I am holding my breath by lordvalrole · · Score: 4, Insightful

    My mother has MS and I know others as well that have it. It is such a horrible disease. I hope this research continues and is a viable option and soon. Nothing is worse than seeing a parent or loved one just lose their abilities over a few years.

    1. Re:Well, I am holding my breath by NoobixCube · · Score: 2, Informative

      My mother has MS as well, and there's only so much Betaferon can do to slow the pace. Just five years ago she was only a little night-blind, as many healthy people are. In that time she's lost her sight totally twice, and now she's losing all colour vision, and has no peripheral vision. And that's the least of the problems MS is causing her.

      --
      Admit it. You post strawman arguments as AC so you get modded Insightful for refuting them, rather than Troll
  5. Re:Snuh! by sumdumass · · Score: 0, Offtopic

    lol.. well, it was the goo err glue that bound the president to the accusation. changing this DNA could have changed history.

  6. MS anecdonte by ookabooka · · Score: 4, Interesting

    First off, IANAD, though both my mother and aunt are. My aunt has fairly severe MS, she can't walk, lost some dexterity in her left arm, etc. What is interesting is that my mother is an identical twin, and doesn't suffer from MS at all. They did some experimental treatments utilizing this unique situation, one of which was some sort of combination of Chemo therapy and a bone marrow transplant. Does this vaccine simple get rid of some "risk factors" in the DNA? Obviously I'd find it hard to believe that there is a direct relationship between DNA and MS. . .

    --
    If you are about to mod me down, keep in mind that this post was most likely sarcastic.
    1. Re:MS anecdonte by timmarhy · · Score: 1

      Why couldn't it be genetic? by your logic all identical twins would die of the exact same things. environment can be the trigger for many illnesses.

      --
      If you mod me down, I will become more powerful than you can imagine....
    2. Re:MS anecdonte by ookabooka · · Score: 1

      Well in that case the genetic factor are risk-factors and not definitive. There are many genetic diseases where you WILL develop symptoms if your DNA is a certain way. I'm saying I don't think MS has such a direct link to DNA based on my anecdotal evidence. That is why I'm questioning exactly what this "DNA vaccine" is doing.

      --
      If you are about to mod me down, keep in mind that this post was most likely sarcastic.
    3. Re:MS anecdonte by Anonymous Coward · · Score: 2, Interesting

      "What is interesting is that my mother is an identical twin, and doesn't suffer from MS at all."

      It is thought that there are triggers for this. I had a friend that made it to 35 before MS started to take place...ended up getting mono and it was only after that that she start to see problems. There are doctors that say the epstein-barr virus is one of the MAJOR triggers for this disease.

      For me, I have another auto-immune disease. Similar in reaction in the immune response, but attacking different parts...I had an accident that left me bed ridden for a few months, and never healed properly. Doctors couldn't figure out why something like that just wasn't healing...turns out my undiagnosed autoimmune was killing any repairs. A simple injection every few days got me out of bed. They tell me in my case that my body hit such a low that the disease was able to take over, and that if I had never had the accident, I probably would never have seen any symptoms.

      "Obviously I'd find it hard to believe that there is a direct relationship between DNA and MS. . ."

      And this is where your obvious belief is entirely wrong. The DNA creates the disposition, some people get it enough that it expresses itself on its own. Others need it and a combination of other external factors to express itself. We all know that almost every part of the human experience is both internal and external. You might have the genes to be a genius, but if you are adopted by ozark hillbillies living in a trash dump, you will most likely never express the genius genes (even if you end up 50% smarter than your siblings, that isn't a consolation).

    4. Re:MS anecdonte by 0123456789 · · Score: 4, Interesting

      I remember a radio programme about identical twins a while ago. One of the things that fascinated me was that although identical twins have identical DNA, their active genes are not identical. Over time, the genes that are active vary between the two twins, as shown by comparing the gene sequences of pairs of identical twins at different ages. The variation was called something like 'Epygenetic modification'. Hopefully someone who knows more about this can comment?

    5. Re:MS anecdonte by krishn_bhakt · · Score: 1

      DNA acquires sporadic mutations. In simple terms, the are the mutations which were not there in beginning but due to defective DNA replication error correction, gets into the DNA) as we age. For e.g., Retinoblastoma is a genetic disease, but 95% of it is sporadic.
      MS is a disease where the protective covering of neuron's conduction channel (axon) called myelin is lost. This in some cases is attributed to the loss of myelin basic protein. Here the researcher has reintroduced the gene for this protein and successfully expressed it as well.

      --
      The Answer Lies in The Genome
    6. Re:MS anecdonte by Anonymous Coward · · Score: 0

      I'm an identical twin, and I've known forever that although our DNA was identical at the time of the egg splitting, the active DNA must be changing as time goes on. This is obvious from the slight differences we have from each other. He's an inch taller than me, for starters.

      We both have HNPP (Hereditary Neuropathy with liability for Pressure Palsies) which we inherited from our mom, though. It is very similar to MS, in that it affects the myelin covering of the nerves, except that it isn't caused by an autoimmune response. Basically a "weak myelin layer" gene somewhere has been switched to the opposite of what it should, and this causes pressure or repetitive stress to damage the nerves more easily than usual. The symptoms are similar to MS, but less severe.

    7. Re:MS anecdonte by Anonymous Coward · · Score: 0

      We both have HNPP (Hereditary Neuropathy with liability for Pressure Palsies) which we inherited from our mom, though. It is very similar to MS, in that it affects the myelin covering of the nerves, except that it isn't caused by an autoimmune response.

      So, are you going to have kids?

    8. Re:MS anecdonte by DerangedAlchemist · · Score: 1
      Generally people mean things like cystic fibrosis as a genetic disease, being something that's caused by specific genes. So if one twin has cystic fibrosis, the identical twin will definitely have it. So MS is not a genetic disease

      What you're describing are genetic risk factors, which do seem quite common for some diseases too.

    9. Re:MS anecdonte by damn_registrars · · Score: 3, Informative

      The term you are looking for is "epigenetics".

      It generally refers to gene regulation via mechanisms beyond DNA sequence. A good example of this is what is called "x chromosome silencing" in all women. While women have two equivalent X chromosomes, one is "permanently silenced" during very early development. This ensures that all of the woman's cells will read X chromosome genes from the same chromosome. No pattern for this has been demonstrated, to the best of my knowledge (as far as favoring paternal vs maternal or anything of that nature).

      A more complicated epigenetic mechanism is via the http://en.wikipedia.org/wiki/Histone_code/. While the code itself is still very much under investigation, it has shown many important traits in gene expression as time and conditions vary for an organism.

      --
      Damn_registrars has no butt-hole. Damn_registrars has no use for a butt-hole.
    10. Re:MS anecdonte by sandarB · · Score: 1

      When I was diagnosed with MS 10 years ago, I was given some statistics. There is ~ 1/1000 chance of any person having MS. If one identical twin has MS, there is a 50% chance the other twin will have it. It is not 100% genetic, but is strongly so.

  7. oops! by Anonymous Coward · · Score: 0

    i just hope it doesnt mess with the sex chromosomes- wouldn't that be fun to explain.

  8. No it does not - how it works by backslashdot · · Score: 4, Insightful

    Multiple sclerosis is when your immune system attacks a nerve's covering called myelin. What the vaccine does is it gets the immune system to stop targetting the myelin by causing a reduction in the T-cells that attack it. If it works as they say, and have demonstrated, it only reduces the number of T-cells that target the myelin protein, not other stuff.

    1. Re:No it does not - how it works by ookabooka · · Score: 1

      Yeah that makes sense. Thats probably why they nuked my aunt's bone marrow and replaced it with my mothers. If I recall correctly it did stop it for a while but ended up being more of a stopgap than a viable treatment. I remember my mother telling me something like if they did that on a normal person the replacement marrow could have aggravated the auto-immune bit more but since they were identical twins there was no fear of rejection.

      --
      If you are about to mod me down, keep in mind that this post was most likely sarcastic.
    2. Re:No it does not - how it works by Thyrteen · · Score: 2, Interesting

      For those who don't know, myelin is a coating that coats the axon of a nerve, promoting signal propogation to the dendrites of the next nerve. Lack of this coating is also known to lead to things such as high impulsivity (This myelin coating does not entire form until at least mid-twenties, and is at least partly responsible for the way we act as kids / teenagers).

    3. Re:No it does not - how it works by Veetox · · Score: 1

      Furthermore, your stem cells actually recombine DNA well after conception to form a completely unique "ID tag" and set of antibody "master codes" - it's sort of like recompiling your OS or customizing your distro. So, it follows that everyone, even identical twins, has a completely different immune system, and that is why one twin could get MS and the other couldn't, but have the same basic genetic structure.

    4. Re:No it does not - how it works by Kennita · · Score: 1

      An axon without its myelin sheath conducts signals much more slowly (IIRC, about 10% the speed) of one with it, with the result that (for example) reaction time is slowed significantly. Most kids/teenagers have quite quick reaction times, IIUC. I think the impulsiveness has some other explanation.

  9. therapeutic DNA vaccine - Gene therapy you dolts! by Anonymous Coward · · Score: 2, Insightful

    Good grief, why don't they just get on with it and call it gene therapy. All this 'therapeutic DNA vaccine' is it because you think people will be scared by something genetic?

    ZOMG! zombie mutant viruses NO WAY!

  10. !!! Yay by robpoe · · Score: 1

    I surely hope that this vaccine is proven safe, and is available in the USA VERY SOON!!!

    I have a close relative with MS and know several others..

    --
    = Grow a brain...
  11. Re:therapeutic DNA vaccine - Gene therapy you dolt by jdigriz · · Score: 1

    Hell, some of these dolts are scared by the 'vaccine' part of it.

  12. "DNA vaccine" by Beryllium+Sphere(tm) · · Score: 4, Informative

    http://en.wikipedia.org/wiki/DNA_vaccination

    DNA is the active ingredient of the vaccine, if they mean what people usually mean by "DNA vaccine".

    To vaccinate against a pathogen, you'd take some gene from it that codes for a surface protein, inject that DNA into muscle cells, let them express it and produce the protein, and the immune system would learn to react.

    Which leaves plenty of confusion, since the goal of MS therapy would be to turn off the immune response to myelin, not to create an immune response.

    This isn't about gene therapy.

  13. Sign me up by j.a.mcguire · · Score: 1

    I'd take a cure for eczema any day, I think people don't appreciate the kind of pain n eczema sufferers go through on a daily basis, just showering each morning is agony, and they still expect you to get into work all bright and cheery! Last I read, 1 in 4 people suffer from eczema with varying theories on its cause ranging from poor regulation of body temperature to diet, to genetics. It's all horse, frankly it showed me from an early age how weak our medicine arsenal is when I am explained on every visit to the docs that the continued use of steroids is the only way to abait the eczema induced pain.

  14. Itsnotlupus by ShakaUVM · · Score: 0

    Remember, it's not lupus.

    http://itsnotlup.us/

  15. this are great news.... by quantic_oscillation7 · · Score: 1

    since i was 25 i got crohn disease, i had acne since i was 15, and after 10 years i was full of that stupid disease so i took this peace of crap - http://www.drugs.com/accutane.html - and as a present i got crohn and my acne didn't disappear :( i'm living with those two for 11 years and believe me, it's not easy... i'm really happy... http://www.crohns.org/treatment/vaccine.htm i hope it will help others too...

    1. Re:this are great news.... by Anonymous Coward · · Score: 0

      Hear, hear. My story's almost identical to yours. I had horrible, cystic acne when I was a teenager and got put on Accutane. Experienced viciously bad side effects from it and tried to kill myself twice. Discontinued and felt fine, but a couple of years later, I needed three surgeries for intestinal problems and the diagnosis was in: Crohn's Disease. Now I'm 29 and I've had this disease for seven years. It's decimated the majority of my 20s and it's likely that I won't be able to live my dream of completing my PhD since I'm currently bed-ridden and that doesn't look to change any time soon.

      I'm really hoping that Professor Hermon-Taylor is able to raise the money to test his vaccine and that it works. This could prevent huge amounts of incredible suffering... I would donate all I could if I had something to give (as a grad student, I really don't).

  16. safe?, maybe, effective? too early to tell by drjzzz · · Score: 2, Interesting

    The article reports the findings from 30 patients - meaning that the trial was testing only whether the therapy was safe. The authors' note that most patients did not progress (to develop worse disease) is only parenthetical, though the information can be used to estimate how many patients will have to be tested to determine efficacy. Frankly, I don't see a solid rational for a therapeutic mechanism, but if it works, great, and we'll learn something about MS and immunology in figuring out how it works.

    There is an extremely effective new therapy for MS that blocks immune cells (lymphocytes) from their normal "trafficking" through the brain. Since the lymphocytes are responsible for the neuronal damage that underlies MS, the symptoms of MS did not worsen in the vast majority of the thousands of patients who used the drug. Unfortunately, in a small number of patients, the lymphocytes are also responsible for controlling a virus that is latent in their brain. In some of these patients, the virus became active and some patients died before the cause was recognized. Here is a link to the abstract of a free research paper that summarizes current understanding. I have no financial interest in the success of this drug (generic name = natalizumab, trade name = Tysabri).

    --
    to err is human, to forgive is divine, to forget is... umm...
  17. Good news by smooc · · Score: 1

    This is very good news if it really works out. There have been many treatments claiming the Holy Grail before, but did nothing much except for the side effects. MS is arguably one of the worst illnesses around. My older brother suffered from it from the age of 19 until he died at the age of 32. The illness itself might not be the worst, but rather the knowledge that it will never get better is what is so hard. My brother graduated tax law with honors, but he had to stop working after a year because of his degrading eyesight. And besides physical inconveniances there are also the pshychological consequences. Remember it attacks all nerves: it changes personalities of people as well.

    That said I really hope that this is what is seems it is.

    --
    - In Memoriam: Jeroen de Bruin (1972-2004), bye bro
  18. simplex by Anonymous Coward · · Score: 0

    Hoping that one day we will get one for the most irritating disease, herpes, aswell...

  19. Why do they call it Multiple Sclerosis.... by Anonymous Coward · · Score: 0

    Can't you just get one?

    1. Re:Why do they call it Multiple Sclerosis.... by Anonymous Coward · · Score: 0

      Because the disease is defined by multiple attacks. If it just happens once, doctors consider it something else.

    2. Re:Why do they call it Multiple Sclerosis.... by mbowersox · · Score: 3, Informative

      Can't you just get one? Sclerosis = Scar Tissue

      Multiple Sclerosis = Multiple areas of scarring in the CNS (Brain, Spinal Cord, Optic Nerves)
  20. Great news... by mbowersox · · Score: 1

    As someone suffering from MS, this is great news. Currently there are few options to treat the disease, and none are guaranteed to work. If they do work, its marginal at best. :( Currently, I take a weekly injection of interferon to try to slow down disease progression, but it can only slow the disease down at most 30-40%. Hopefully in my lifetime the disease progression can be stopped dead in its tracks. This is a good start...

    1. Re:Great news... by 3waygeek · · Score: 1

      My mom has had MS for about 15 years now -- for the last 10 or so years, she's been taking daily injections of Copaxone, which seems to have stopped the disease in its tracks. Fortunately, dad has good insurance -- the Copaxone runs about $2000 per month.

    2. Re:Great news... by Kennita · · Score: 1

      Mitoxantrone (trade name: Novantrone) is a relatively new treatment that can indeed stop MS in its tracks, and sometimes even (as in my case) back it off somewhat, though it's not a cure. For the clinical trial that shows a statistical reduction in disability, see novantrone.com -- under the Multiple Sclerosis heading, click the Professionals button, then look at the Prescribing Information (PDF).

  21. Confusing terminology by slapout · · Score: 1

    Wouldn't a "DNA vaccine" be something that keeps you from getting DNA? Like the way the Polio vaccine keeps you from getting Polio?

    --
    Coder's Stone: The programming language quick ref for iPad
    1. Re:Confusing terminology by Anonymous Coward · · Score: 0

      Hibbert: (after giving Bart a shot) There, that's six years worth of inoculations.
      Homer: (hands Hibbert a roll of money) There you are, my good man. And while you're at it, throw in one of those polio shots.
      Hibbert: Ooh, yes, sir. (picks up a needle)
      Homer: Eh ... anti-polio.
      (Hibbert picks up a much bigger needle)

    2. Re:Confusing terminology by Anonymous Coward · · Score: 0

      Nope, the summary clearly specified "therapeutic" vaccine. This means it's not a preventive vaccine.

  22. Treatment for other diseases by Reeli · · Score: 1

    The researchers say if it all goes well, that it's possible that antigen-specific DNA vaccines could one day be developed for treatment of related diseases, such as type 1 diabetes, lupus and rheumatoid arthritis. My mother has rheumatoid arthritis, and while it's not as bad as MS, it's certainly had its toll on her. DNA vaccines seem to be very promising, and I hope that the research begins to bring real results.

  23. Cool work by Pedrito · · Score: 3, Interesting

    I haven't read the details of the study, but here's what's basically going on, from what I can tell so far... MS is a disease in which the immune system attacks the myelin in Schwann cells. Myelin is an "electrical insulator" in the cell membrane of Schwann cells. Schwann cells wrap around the axons of nerve cells in segments and the electrical signal basically jumps across the Schwann cell segments, increasing the speed of conduction. In MS, the body's immune system sees myelin as a foreign invader and attacks it and slowly consumes the myelin, eventually making the nerves non-functional.

    The vaccine is actually a virus. It doesn't say specifically in the article, but I suspect it's an adenovirus because they're pretty good for this kind of thing. The DNA sequence for the Myelin basic protein (MBP) is encoded into the virus. There are actually several variants of MBP and I'm curious if they're introducing just one variant or multiple variants. Anyway, MBP is involved in myelination of nerves. I don't think this part is well understood, but in studies of mice where the gene for myelin basic protein has been removed (mice with a certain gene or genes removed are called knockout mice), they develop diseases similar to MS.

    Anyway, it's cool stuff and this kind of technology is really the future of treatment for a lot of diseases. There's a protein called p53 that's involved in the normal regulation of cell death and when the gene for P53 gets mutated, it can lead to cancer. p53 is implicated in roughly half of all cancers. One possible treatment is to come up with an virus with a normal p53 gene encoded in it and use that to turn the cancer cells back into normal cells that die properly. There are a host of other genetic based diseases where this kind of thing could be useful as well.

    1. Re:Cool work by drjzzz · · Score: 3, Interesting

      I haven't read the details of the study, but here's what's basically going on, from what I can tell so far...
      X SNIP X
      The vaccine is actually a virus. Wrong. A poster describing the work is available for download from the company, Bayhill Therapeutics, here. The therapeutic is not a virus but rather a relatively simple, circular DNA (plasmid) of about 3,500 nucleotides with a promoter to drive transcription (make mRNA) and a polyadenylation site to stabilize the mRNA. Otherwise, the DNA has just the minimum to grow and select in bacteria (origin of replication and antibiotic resistance gene that is inactive in humans). Once injected into an animal, such pure DNA is thought to be picked up by specialized phagocytes ("eating cells") that are able to make the encoded protein, albeit at low levels, and trigger immune cells with fragments of the newly made proteins.

      What's odd, is that immunization with MBP can provoke an MS-like disease in mice of some strains. An abstract to an open-source paper is here. So exactly how this is working as a therapeutic is (more than a little) obscure.
      --
      to err is human, to forgive is divine, to forget is... umm...
    2. Re:Cool work by aznop · · Score: 1

      As an MS patient myself, I've done a bit of research on the disease. I disagree with your characterization of what MS is. Schwann cells are part of the peripheral nervous system, where MS is primarily a disease of the central nervous system. Myelin in the central nervous system is provided by oligodendrocytes. I feel that the parent post is inaccurate and misleading.

  24. Directions in MS research by Anonymous Coward · · Score: 2, Informative

    GSASoftware wrote:
    > The cause of the disease is not fully understood, but it appears to
    > be auto-immune.

    It is auto-immune; there is no question about that, and there hasn't
    been for a few decades now.

    I was diagnosed with Multiple Sclerosis in 2000; I got my first
    symptoms when I was 19 years old while I was overseas (imagine waking
    up one morning with half your vision gone in one eye). My mother has
    MS too. That there is a genetic factor has always been
    known. Typically, if a close relative has MS, you have about a 3%
    chance of developing the condition yourself (I won that lottery). One
    popular theory is that there is a substantial number of genes that
    have to possess certain characteristics in order for a person to be
    predisposed to developing the condition, and then exposure to some
    pathogen triggers the immune system to learn to attack the myelin
    around the axons. MS is so strange a disease that experts are not
    quick to jump onto any one bandwagon in terms of what actually causes
    MS.

    The recent findings by Dr. Stephen Hauser's team have identified the
    IL2R and IL7R genes as specifically involved, and it will likely be
    the case that several more genes will be correlated. It is only very
    recently have actual genes been linked to the condition (and my
    personal belief is that the anti-stem cell research position of the
    U.S. government has been and will continue to be a major hindrance in
    genetic research on MS, but that is for another thread).

    There is more good news; Dr. Giovanna Bersellino's team has recently
    identified another subgroup of suppressor cells that tend to be
    diminished in patients with MS:

    http://idw-online.de/pages/de/news221805

    The medication I am currently taking (interferon beta-1a injections)
    is the best known-safe treatment we have, but it really is not that
    much different from what has been being used since 1993. The thing is,
    nobody really knows exactly why it works; the info sheet that ships
    with my medication reads, "The specific interferon-induced proteins
    and mechanisms by which interferon beta-1a exerts it effects in
    multiple sclerosis have not been fully defined." On average, it slows
    clinical progression (number of lesions in the nervous system) by
    about 30%, but MS and its treatments are ellusive. It could be very
    mild or very aggressive, and various medications can be very effective
    or completely ineffective for different people with MS.

    Other possible treatments under investigation include cladribine,
    fingolimod, BG00012, MN-166, SB-683699, teriflunomide, atorvastatin
    calcium, BHT-3009-01, CNTO 1275, daclizumab, rituximab, Estriol,
    ABT-874, Cyclophosphamide, methylprednisolone, MBP8298, Fampridine-SR,
    Lamotrigine, tetrahydrocannabinol, and so on. MS is a really hard
    problem, and scientists are hitting it from all kinds of different
    directions. MS requires several cures. We need to figure out what gets
    it to start in the first place and to prevent it from happening at
    all. We need to stop the disease in its tracks for those who have
    already developed it. Finally, we need to repair the damage that has
    been done to the nervous system.

    This new vaccine is good news, but people with MS have learned to curb
    their enthusiasm whenever new research discoveries are made. All too
    often, promising new treatments turn out to have life-threatening side
    effects (messing with how your immune system does its job in your
    brain is tricky business).

    1. Re:Directions in MS research by jesup · · Score: 1

      You may be referring to the very recent study of a large number of people (thousands) in the UK using "gene chips" to identify common loci of different genetic diseases. MS apparently shares some susceptibility genes/loci with other auto-immune diseases, such as type-1 (juvenile) diabetes and Crohnes disease (sp). See Science News, or MIT Technology Review I think.

    2. Re:Directions in MS research by drjzzz · · Score: 1

      Here is a large collaborative study just published in the New England Journal of Medicine (free text with registration).

      The "common gene" hypothesis almost certainly explains disease that "runs in families". The influence of these genetic variants (alleles) tends to be low, so families my have several different susceptibility alleles combining to produce disease. There is another, intriguing hypothesis that may explain the many people with disease who do not have many, or any, susceptibility alleles. This hypothesis suggests that mutations within a single immune cell may allow it to escape normal regulatory mechanisms and produce disease. It is analogous to the cancer mutation theories - some inherited from ancestors, some developed during life. This hypothesis was recently reviewed, link here (not free but you can explore from the abstract).

      These two competing/complementary hypotheses constitute a good example of how science moves forward.

      --
      to err is human, to forgive is divine, to forget is... umm...
  25. Re:Snuh! by Anonymous Coward · · Score: 0

    It's spelled "Clinus".

  26. Sick and Tired by techpawn · · Score: 1

    I every time someone claims to of found a "cure" for MS I shutter. I know it's far too lucrative for big pharm to lose. When a single monthly box of my injections cost over 2 grand? I mean, let's be honest with ourselves kiddies. I'm not expecting a cure anytime soon and neither should you. This is modern day snake oil because they bank on us being such a hopeless lot. We're given about 50 years, the knowledge that we're just going to get WORSE and then told how much our meds cost. Any glimmer of hope seems good until you become cynical. Diagnosed 2004

    --
    Ask not what you can do for your country. Ask what your country did to you
    1. Re:Sick and Tired by Slashdot+Parent · · Score: 1

      I'm sorry to hear that you have become cynical.

      One thing that is "nice" about MS, is that there is a large enough population of affected people that a lot of research is being done. This is compounded by the cross-application of many therapies between MS and Crohn's, rheumatoid arthritis, fibromyalgia, etc. At least it isn't some obscure disorder that doesn't get any research at all.

      Biogen Idec definitely has a great thing going from a balance sheet perspective, I'll grant you. But they know that if some other pharmaceutical company comes up with a vaccine, there won't be any more Avonex or Tysabri customers.

      Good luck!

      --
      They don't grade fathers, but if your daughter's a stripper, you fucked up. --Chris Rock
    2. Re:Sick and Tired by Slashdot+Parent · · Score: 1

      Is that per dose, or per month? As I'm sure you are aware, Tysabri is administered once per month, whereas Avonex is administered weekly, and Rebif is administered three times per week.

      Also, Tysabri is an IV drip instead of an injection, so it must be administered in a provider office. Avonex and Rebif are typically self-administered (or administered by a spouse, parent, etc.)

      --
      They don't grade fathers, but if your daughter's a stripper, you fucked up. --Chris Rock
    3. Re:Sick and Tired by sandarB · · Score: 1

      I agree! I think I have been more crippled (in terms of being able to live the life I want, and pursue my goals) by the cost of meds, and the necessity of having group health insurance, than I have been by the actual disease.

    4. Re:Sick and Tired by techpawn · · Score: 1

      I can only speak of Rebif. But I get a sick sense of sticking it to the man when I see the amount my insurance "saved me"... I know it's some back room deal, but I'd like to think there's some bean counter screaming each month as they eat the cost... Screwing Insurance and Big Pharm in one trip... At least I'd like to think so, even if it isn't true

      --
      Ask not what you can do for your country. Ask what your country did to you
    5. Re:Sick and Tired by Slashdot+Parent · · Score: 1

      Well, whatever it takes to hit that button in the Rebiject, that's what you should think about. :)

      --
      They don't grade fathers, but if your daughter's a stripper, you fucked up. --Chris Rock
  27. Re:therapeutic DNA vaccine - Gene therapy you dolt by Eli+Gottlieb · · Score: 1

    ZOMG! zombie mutant viruses NO WAY! Flippin sweet!
  28. Never again... by lord_sarpedon · · Score: 1

    ...will people have to live in fear of contracting DNA. It is alarming how widespread it is among people today -- it can be a fatal mistake to assume that you do not already have DNA. Seek medical care immediately for treatment of symptoms. I really can't stress this enough: virtually every living thing with DNA will *DIE* within a matter of decades! Please, make sure your children get this vaccine before it's too late for us all.

    --
    "Strangers have the best candy" -Me
  29. Not DNA per say but some coding of the immune by crovira · · Score: 1

    system gets screwed up, either through an inheritable pre-disposition to environmental triggers or through the action of those environment triggers.

    I am a not a doctor but I DO have MS.

    MS may be a syndrome for a whole bunch of DNA/RAN transcription errors which can either be ignored because the triggers never occur or which can really fuck up your life by transforming what would normally just be a sneeze (an allergic reaction) into a life-threatening episode.

    I never get the flu, I get episodes of MS instead (or "as well as').

    --
    MSBPodcast.com The opinions expressed here are my own. If you don't like 'em... Think up your own stuff.
  30. Why such offense? by Slashdot+Parent · · Score: 2, Insightful

    I'm unclear as to why you took so much offense to the GP's attempted humor.

    His joke itself, of course, was not funny. It's a play on the wording of the title. Instead of parsing it as a DNA vaccine against MS, he parsed "DNA Vaccine" as a vaccine against DNA. The attempted humor being, if you don't want to be "infected" with DNA, use a condom.

    You somehow interpreted his joke to imply that MS was caused by unprotected sex. I didn't read the post that way, and anyhow, I have never heard anyone suggest, either credibly or in jest, that MS is an STD.

    In fact, I found the "joke" to only be making fun of the article's title, and not MS itself. As hard as I try, and as many angles as I search, I am unable to come up with any situation in which MS could be humorous.

    Wife diagnosed in '05.

    --
    They don't grade fathers, but if your daughter's a stripper, you fucked up. --Chris Rock
  31. Re:Always a possibility - Multiple Sclerosis Cures by origins101 · · Score: 1

    I come from a family of research scientists personally afflicted with 5 cancers and 4 autoimmune diseases, and I would like to say that "Possibilities" are what keep us on our technical toes, help us "connect the discovery dots" and give hope to patients and those that love them. Our team is currently working on graph theory network maps (similar to those you might find in "WIRED" showing all the servers communicating over the web) that link all known drugs, diseases, biological agents and successful clinical outcomes reported in the peer-reviewed evidence (1949-2007>). Our model applies mathematical weights to each connection (edge) and then seeks to calculate the probability that DRUG A used for RELATED DISEASE 1...might also CURE...DISEASE 2, 3, ...n. You might think of this "Network" as a special type of TCP: Transmissive Curative Packet Net where drugs "talk to diseases." We test the model by going back in time in the data to see if the connections, scientific observations, made between 1949-1989 are strong and can predict drug applications that would not emerge until 1999, for example. What we find over and over again is that drug history often can predict drug future uses accurately. Good examples in the autoimmune family of diseases are two now quite old meds: Methotrexate-1949 and Cyclosporin(e)-1978. Originally developed for cancer and graft-vs-host disease, they emerged into mainstays for the autoimmune disease family and proved effective against psoriasis, eczema, arthritis, lupus, lichen planus, pemphigus, and numerous other skin diseases. The first step in such methods of network discovery "by relational possibility" is computing the central hub in the drug-disease-agent relationship. TNF or tumor necrosis factor is one agent that demonstrated "centrality" in drug-disease cause/cure maps early on and became a leading indicator of an over active immune system central to both many cancers and related autoimmune responses. For MS our system as of today would suggest that Copolymer 1(Also named Copaxone and Glatiramer Acetate), Methylprednisolone, Mitoxantrone, and some of the more potent immune suppressors would be helpful. Two weeks ago we put a BETA site online where patients can get top down drug recommendations of the system just by entering their disease name in a Google-like search field at the top page. Currently we are restricting access to the full research interface to licensed physicians as we continue to check the data integrity of the system, but both the patient search and the physician access are free so if you want to take a look at the network maps with your doc, you can. In sum looking at possibilities for cures is how we find them, convert observation to association to correlation to causation and then to understanding of the complete mechanism of disease. So we advise all patients to take their "suspicions" to their docs and to their medical librarians and see if just maybe your insight has merit. The one discussed in this thread does. If you want to learn more: http://www.curehunter.com/public/showTopPage.do [FDA Disclosure: As a principal scientist at CureHunter,Inc. I have a vested interest in the success of our models and methods, but none whatsoever in any specific drug or treatment. Good luck and good hunting, be a patient activist, nobody knows what you are experiencing better than you.]

  32. Re:Always a possibility - Multiple Sclerosis Cures by NelsChristian · · Score: 1
    Ok, try this in your model. This chart is from a presentation by Dr Trevor Marshall, Phd to the Bio21 Institute at the University of Melbourne. (reference here)

    Phase 2 Cohort/Recover Statistics
    Phase 2, open label, observational community-based study

    (see page 5 of this pdf)

    7 of 8 Rheumatoid Arthritis
    20 of 25 Hashimoto's Thyroiditis
    4 of 5 Osteo-Arthritis
    40 of 77 CFS/CFIDS/ME
    9 of 15 Cardiac Arrythmia
    57 of 92 Sarcoidosis
    3 of 5 Diabetes
    12 of 18 Uveitis
    20 of 34 FMS
    8 of 10 IBS
    Here you have a study showing recovery (i.e. cure), not just palliation, for very significant proportions of the study group (>50%). For myself, I was diagnosed with IBS, then sarcoid, then diabetes. The diabetes is gone, and there are only fading shadows of the problems from the other two.

    And, this is reasonable simple protocol, using well known antibiotics and one ARB.