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Immunosuppressants


Celiacandme

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Celiacandme Apprentice

I'm just curious if anyone here has had to take immunosuppressants because of their celiac disease? If so, were you able to come off it after some time? What made the determination that your body needed to take it? Did you notice a difference?
 

If anyone has anything to share regarding celiac disease and immunosuppressants, I'd love to hear it.

 

Thanks so much!

  • 1 month later...

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Nicki Raeleen Rookie

Omg finally someone!!!! YES! I have just been  prescribed  them for my celiac. My GI doctor told me it's extremely rare.

they determined I needed to take it because even after blood test, food long, simple diets, and MRIs looking for  lymphomas, my body was still producing an extremely high level of antibodies (about 27-35). I haven't started them yet, but my sister has chrons so she takes a much high does of them and tell me the side effects are worth the results (if it even works). 

CeliacBurger Newbie

Have you looked into Low Dose Naltrexone?  Or LDN.  My understanding is that it can be extremely helpful as an immune modulator for people with celiac, without resorting to prednisone or other heavy duty immune suppressants.   Google it and see what you think. 

Nicki Raeleen Rookie

I looked it up and it looks very fascinating. I couldn't find much correlation between it and suppressing immune systems. Something did occur to me though ( I feel a bit silly saying it out loud), that maybe my Celia isn't the problem at all. They are putting me on the immune suppressants to make me feel well enough to do more testing. Even though my tTG, Atg, and other levels related to celiac are extremely high, maybe it might be something more serious. The Celiac was just the scapegoat. 

I have head of some non-responsive celiac patients developing other autoimmune diseases over time ( like Crhons, lupus, and cancer) witch would explain why the go to would be immune suppressors. 

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      Thanks to both of you for your responses!  Sadly, even after several years of very strict gluten avoidance, I remember the symptoms well enough that I am too frightened to risk a gluten challenge— heartbeat and breathing problems are scary— Scott, thank you for the specific information— I will call around in the new year to see if I can find anyone. In the meantime, I will carry on has I have been— it’s working! Thanks also for the validation— sometimes I just feel crushed by disbelief. Not enough to make me eat gluten though—
    • trents
      Welcome to the celiac.com community, @GlorietaKaro! As Scott indicated, without formal testing for celiac disease, which would require you to have been consuming generous amounts of gluten daily for weeks, it would be not be possible to distinguish whether you have celiac disease or NCGS (Non Celiac Gluten Sensitivity). Their symptoms overlap. The difference being that celiac disease is an autoimmune disorder that damages the lining of the small bowel. We actually no more about celiac disease than we do about NCGS, the mechanism of the latter being more difficult to classify. There are specific antibody tests for celiac disease diagnosis and there is also the endoscopy/biopsy of the small bowel lining. Currently, there are no tests to diagnose NCGS. Celiac disease must first ruled out. Researchers are working on developing testing methods to diagnose celiac disease that do not require a "gluten challenge" which is just out of the question for so many because it poses serious, even life-threatening, health risks. But we aren't there yet.
    • lalan45
      That’s really frustrating, I’m sorry you went through that. High fiber can definitely cause sudden stomach issues, especially if your body isn’t used to it yet, but accidental gluten exposure can feel similar. Keeping a simple food/symptom journal and introducing new foods one at a time can really help you spot patterns. You’re already doing the right things with cleaning and separating baking—also watch shared toasters, cutting boards, and labels like “may contain.”
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      I thought this might be of interest regarding anti-EMA testing. Some labs use donated umbilical cord instead of monkey oesophagus. Some labs just provide a +ve/-ve test result but others provide a grade by testing progressively diluted blood sample. https://www.aesku.com/index.php/ifu-download/1367-ema-instruction-manual-en-1/file Fluorescence-labelled anti-tTG2 autoantibodies bind to endomysium (the thin layer around muscle fibres) forming a characteristic honeycomb pattern under the microscope - this is highly specific to coeliac disease. The binding site is extracellular tTG2 bound to fibronectin and collagen. Human or monkey derived endomysium is necessary because tTG2 from other mammals does not provide the right binding epitope. https://www.mdpi.com/1422-0067/26/3/1012
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