Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Celiac Treatment Research


Mollifier

Recommended Posts

maile Newbie

I have to admit I'm skeptical for a couple of reasons, first given how darn difficult it is to diagnose and how few have actually been diagnosed I'm surprised they'd be able to find a "cure" for something they can't even identify in 2/3 people. <_<

secondly the whole "injecting with gluten" part of the trial....there have been huge debates in this forum alone on the topic of whether one can be affected by gluten if it isn't digested/ingested through the GI system. in fact I'd understood (and am totally aware I could be mistaken) that the antibodies only show in the blood when there is sufficient villus atrophy to cause a leak into the blood. And, in order to figure out if the vaccine works they're going to use blood tests (which appear to be reliable only when celiacs are at or near the end stage of the disease) to diagnose whether or not you are being affected???

I'm not a medical professional so I could be missing something but it just seems a bit odd.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



LandonL Contributor
I have to admit I'm skeptical for a couple of reasons, first given how darn difficult it is to diagnose and how few have actually been diagnosed I'm surprised they'd be able to find a "cure" for something they can't even identify in 2/3 people. <_<

secondly the whole "injecting with gluten" part of the trial....there have been huge debates in this forum alone on the topic of whether one can be affected by gluten if it isn't digested/ingested through the GI system. in fact I'd understood (and am totally aware I could be mistaken) that the antibodies only show in the blood when there is sufficient villus atrophy to cause a leak into the blood. And, in order to figure out if the vaccine works they're going to use blood tests (which appear to be reliable only when celiacs are at or near the end stage of the disease) to diagnose whether or not you are being affected???

I'm not a medical professional so I could be missing something but it just seems a bit odd.

So are you saying that if someone tested positive on the blood test they are at or near the end of the disease? and what does that mean, what do you mean by end of the disease? I tested positive through prometheus blood testing. I also had a biopsy, and My GI told me I had a marsh score of 1 which he told me was good cause that meant we caught it eary, so you have me confused.

maile Newbie
So are you saying that if someone tested positive on the blood test they are at or near the end of the disease? and what does that mean, what do you mean by end of the disease? I tested positive through prometheus blood testing. I also had a biopsy, and My GI told me I had a marsh score of 1 which he told me was good cause that meant we caught it eary, so you have me confused.

sorry about that, as I said I'm not a medical professional! I should have said "end stage of the disease" (this is not like end stage of cancer, rather you can be sick for years while ingesting gluten but until you show some sort of damage to the villi you cannot be diagnosed as a celiac)

so as not to confuse you any more here's some links about diagnosis of celiac, stages of the disease and reliability of blood tests:

Open Original Shared Link

Open Original Shared Link

This Link and this other link explain it much better than I ever could.

Lisa Mentor

Open Original Shared Link

This article is about Dr. Kenneth Fine. He is discussing testing through his company and markets to those who's conventional testing has not provide positive results through serologic testing. Enterolabs test via stool testing.

Although many people here have used his services and are strong supporters of Enterolabs, there may be better articles relating to blood testing.

Positive Serological testing is not an indicator that a person is at the end stage of Celiac Disease. Rather, it provides information that your body is reacting to the presence of gluten, by creating antibodies.

Here is some information:

Open Original Shared Link

maile Newbie
Positive Serological testing is not an indicator that a person is at the end stage of Celiac Disease. Rather, it provides information that your body is reacting to the presence of gluten, by creating antibodies.

Here is some information:

Open Original Shared Link

Thanks for clearing my confusion!

Lisa Mentor
Thanks for clearing my confusion!

;):) There is a lot to learn about this stuff. I learn something every day.

caek-is-a-lie Explorer
I think the entire notion of "building up a tolerance" is pure rubbish. I would point out, that many on this board have noticed an increased sensitivity to gluten after being gluten-free for a while. However, the damage to the intestine had still been occurring before the change in diet. Only the appearance of outward symptoms were suppressed.

Well, I do believe there is evidence that desensitization works in some cases. And this group found positive results in doing this treatment in mice. Of course, mice aren't humans, so we'll see how the human trials go. They indicate the treatment takes months to complete.

My issue with the whole thing is in calling it a "vaccine". It's not a vaccine. A vaccine is injecting modified or killed virus into your body that you have not been previously exposed to so that you can make new antibodies against it to fight it off when you are eventually exposed to the illness.

Gluten is not a virus and our whole problem is we already make antibodies against it which then attack our own cells. So this treatment is more like an antivaccine, really. I wish they would just call it what it really is...gluten desensitization. "vaccine" is so misleading! It's not like you get one little shot and you're cured.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,540
    • Most Online (within 30 mins)
      7,748

    Barrie S
    Newest Member
    Barrie S
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
    • Celiac50
      That sounds so very likely in my case! I will absolutely ask my doctor on my next bone check coming up in March... Thanks a lot! 
    • trents
      Calcium levels as measured in the blood can be quite deceiving as the body will rob calcium from the bones to meet demands for it by other bodily functions. Also, supplementing with calcium can be counterproductive as it tends to raise gut pH and decrease absorption. More often than not, the problem is poor absorption to begin with rather than deficiency of intake amounts in the diet. Calcium needs an acidic environment to be absorbed. This is why so many people on PPIs develop osteoporosis. The PPIs raise gut pH. And some people have high gut PH for other reasons. Low pH equates to a more acidic environment whereas high pH equates to a more basic (less acidic) environment.
    • Celiac50
      Kind thanks for all this valuable information! Since my Folate was/is low and also my Calcium, there IS a chance I am low in B vitamins... My doctor only measured the first two, oh and Zinc as I has twisted her arm and guess what, that was mega low too. So who knows, until I get myself tested properly, what else I am deficient in... I did a hair mineral test recently and it said to avoid All sources of Calcium. But this is confusing for me as my Ca is so low and I have osteoporosis because of this. It is my Adjusted Ca that is on the higher side and shouldn't be. So am not sure why the mineral test showed high Ca (well, it was medium in the test but relative to my lowish Magnesium, also via hair sample, it was high I was told). But anyway, thanks again for the VitB download, I will look into this most certainly!
    • ElisaAllergiesgluten
      Hello good afternoon, I was wondering if anyone has ever brought their anti-allergy pills? I have been wanting to use their Cetirizine HCI 10mg. They are called HealthA2Z and distributed by Allegiant Health.I’m also Asthmatic and these allergies are terrible for me but I also want to be sure they don’t have any sort of gluten compound.    I have tried calling them but to no avail. Has anyone ever used them? If so, did you had any problems or no problems at all?    thank you
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.