Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Bacterial Enzyme Renders Gluten Harmless


Emme999

Recommended Posts

Emme999 Enthusiast

Here's a little research I just found regarding an enzyme that supposedly can "neutralize" celiac disease. (I'll stick in the main parts and put the link at the end :))

In the September 27 issue of Science, Chaitan Khosla and his coworkers at Stanford University and the University of Norway in Oslo, report disassembling the large, complex mixture of gluten proteins and identifying a single component that triggers the autoimmune response characteristic of celiac sprue.

The researchers determined that the autoimmune response in people with celiac sprue can be traced to an unusually long molecule - a chain of 33 amino acids - that cannot be broken down by the human digestive system. They immersed the 33-amino acid chain in digestive enzymes derived from bacteria and found that a bacterial enzyme, prolyl endopeptidase, can break the chain into apparently harmless components.

In the small intestine, enzymes from the pancreas initially digest gluten by breaking it into a number of fragments called peptides. In most people, the larger peptides probably work their way down to the lower intestine where they are eaten by microorganisms.

"But in people with celiac sprue, the stable 33-amino acid peptide causes big problems because the molecule is recognized as being a threat to the person's immune system,"

Khosla and his coworkers believe the bacterial enzymes, which worked in human tissue cultures as well as intact rats, may result in a simple, oral supplement that can eliminate the harmful effects of gluten. The treatment approach would be similar to enzyme supplements taken orally by people who cannot digest lactose, a sugar found in milk.

Khosla adds that an approved therapy could be as many as 5 to 8 years away, although research is already underway and the treatment should be testable in people within 2 to 3 years.

(This research is from 2002)

Here's the link: Open Original Shared Link

Let me know if you've heard about this :)

- Michelle :wub:


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



Celiac.com Sponsor (A8-M):



frenchiemama Collaborator

Can that really be true? I wonder if it's something that you can just take right before you eat like a lactaid, or if it's a daily treatment.

tarnalberry Community Regular

I remember reading about that, and thinking "ok, but is that particular chemical reaction going to finish to completion, and how do you know just how much of the enzyme you need to balance that mass equation". Usually, with lactase, as long as MOST of the lactose is split apart, it's sufficient not to cause any symptoms, but some people are so sensitive, even that's not enough. We're sensitive enough that "breaking up most of the gluten" wouldn't be enough for us either - to prevent damage. So I'll be looking at the follow up testing very closely.

frenchiemama Collaborator

So if this panned out, and rendered gluten totally harmless, would you guys go back to a regular diet? I'm not sure I would. I've come to the conclusion that wheat isn't particularly good for anyone and I've felt so good since going gluten-free that I don't think I'd revert to my pre-diagnosis way of eating. I might use it before eating out at a restaurant though, or on a special occasion, but not every day.

KaitiUSA Enthusiast

I would stay gluten free. This pill may help with symptoms but may still cause damage. I am very skeptical.

Something to help with reactions(that you get by accident) would be nice but as far as I am concerned...I will continue being gluten free

I would have to evaluate further after testing and so forth is done...at this point I am very skeptical of it.

cdford Contributor

As with all new therapies, I would probably take a wait and watch mentality. I do this even with some of the new wonder drugs for other things or immunizations for my kids. I figure if it is still shown to work with minimal side effects after several years, then I'll try it. Even then, I would probably just keep it around for special occasions. I just can't see taking anything else if I don't have to.

pixiegirl Enthusiast

I'd certainly do the new therapy, once it was tested and proved to be totally effective, of course. I think they would be able to tell with endoscopy's if it really worked or if there was still intentinal damage.

Would I change my entire diet to a gluten one again... the answer to that is no, however I was not a huge bread eater/gluten eater before. But it would be nice to go to a restaurant and pop and pill and not have to worry about salad dressings and seasonings and such. I'm eating well now and happy with that but with all the travel I do it would certainly take a lot of the worry out of my life.

Susan


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



Celiac.com Sponsor (A8-M):



jenvan Collaborator

My thoughts are the same as Tiffany's... I would wonder--how could we be sure the supplement would account for every nook and cranny gluten could get it, and every chain we'd ingest? Will be interesting to see what happens....

tarnalberry Community Regular

This sort of treatment, I would consider taking when going out to eat - though I'd still choose items that ought to be gluten-free - or attending special events, but that'd be about it. After two years without bread, who needs it! ;-)

bklyn Enthusiast

I would be thrilled to have a "pill" to take, especially when eating out. I find the hardest part of being gluten free is the constant "worrying" about what to eat. I miss the days of just "grabbing a bite." Eating out was a huge part of my family's social life and now I just can't do it any more without a lot of planning.

jknnej Collaborator

I would stay gluten-free for SURE but agree with Susan. When I have to eat out I get anxiety ridden. If I could take a pill where I knew I wouldn't get sick, I would still order gluten-free but not feel so worried. It would be GREAT!

VydorScope Proficient

That story, as you stated, is dated 2002, anyone know if thier are any updates to it?

  • 1 month later...
celiachap Apprentice

Peptidase supplement product for Gluten ingestion now available

Open Original Shared Link :D

Research at Stanford University School of Medicine regarding Peptidase dietary enzyme supplement:

Open Original Shared Link

Originally posted by Michelle:

Open Original Shared Link

lovegrov Collaborator

Folks, this is NOT a proven treatment for celiac. As the Stanford scientists say, a whole lot more study has to be done. They have no idea if this works inside the human body or even if it did work, how much you would have to take. Do NOT buy this stuff thinking you can take it and suddenly eat all the gluten you want.

richard

pixiegirl Enthusiast

Yes we know its not proven... I think that was said but the question was... if it was proven would you eat gluten regularly and take the "pill" or would you mostly avoid it and use it occasionally.

Personally as I said, my diet it healthier this way but I'd certainly use it when I go out to dinner.

Susan

lovegrov Collaborator

"Yes we know its not proven... I think that was said but the question was... if it was proven would you eat gluten regularly and take the "pill" or would you mostly avoid it and use it occasionally."

Ah, but if you go to the first link celiachap posted, you might think these folks have a proven product for celiac. They do not.

I should have been clearer about what I was refering to.

richard

celiachap Apprentice
"Yes we know its not proven... I think that was said but the question was... if it was proven would you eat gluten regularly and take the "pill" or would you mostly avoid it and use it occasionally."

Ah, but if you go to the first link celiachap posted, you might think these folks have a proven product for celiac. They do not.

I should have been clearer about what I was refering to.

richard

<{POST_SNAPBACK}>

:(

We can wait five, ten, or twenty years until (or if) this product is approved for pharmaceutical use, or we can try it now.

Since the overall tone of the responses to my postings regarding this has been negative, by "advanced members" (lol), I will not bother to post the results of my personal use of this product on this board. :P

skbird Contributor

Uh, that's helpful. I'm not sure I see a major upswelling of reaction by "advanced" members here. I, for one, would be interested, but I'm not going to beg. :P

Stephanie

VydorScope Proficient

IMO, "personal" experence in this case is not very usefull. Unless you have been using it a while. and have had an enscopy to measure if any damage has been done, all you can realy speak to is symptons. I am far more concerned with damage the symptons.

Thats just my opinion, others will disagree I am sure. :)

Emme999 Enthusiast
:(

We can wait five, ten, or twenty years until (or if) this product is approved for pharmaceutical use, or we can try it now. 

Since the overall tone of the responses to my postings regarding this has been negative, by "advanced members" (lol), I will not bother to post the results of my personal use of this product on this board.  :P

<{POST_SNAPBACK}>

Hey I'm interested in your personal experience! :)

- Michelle :wub:

celiachap Apprentice

An Email, from Kirkman Labs, received by one of our Celiac.com members today, in response to an inquiry:

DPP IV Forte is just one enzyme. It does help with casein and gluten, but works better in conjunction with other enzymes. We have several customers who use it together with the Enzyme Aid or Enzyme Complete for when they think they may need extra help

The Enzymaid is specifically for dairy and wheat proteins. It may help with some additional proteins but has nothing for carbs or fats.

Enzym-Complete is a broad spectrum enzyme. Meaning that it helps with all food proteins and carbohydrates and fats it also includes the enzyme DPP IV that is specific to casein and gluten.

We never recommend using enzymes to replace a gluten free diet. They are meant to be an aid to help with hidden gluten or infractions either intentional or accidental. The enzymes break down the proteins, but they may not get every molecule and the effectiveness is going to depend on the sensitivity of the person and the severity of the infraction.

lovegrov Collaborator

This is all I need to see.

"We never recommend using enzymes to replace a gluten free diet."

And from the company's web site.

"These statements have not been evaluated by the Food & Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease."

I've been gluten-free for almost four years and went from very near death to healthy again simply by being gluten-free. That's my experience. Although this company has that warning at the bottom of the web page, the rest of it reads like they've found a cure.

richard

angellove839 Rookie

They always get excited about that sort of stuff. They are close to making money! The better convincing they are, the more the public will want it.

Emme999 Enthusiast
And from the company's web site.

"These statements have not been evaluated by the Food & Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease."

I've been gluten-free for almost four years and went from very near death to healthy again simply by being gluten-free. That's my experience. Although this company has that warning at the bottom of the web page, the rest of it reads like they've found a cure.

richard

<{POST_SNAPBACK}>

That warning is required to be put on *all* supplements & vitamins. It doesn't mean that they don't have any value.

I wouldn't (ever) give up the gluten-free diet because of claims from a company manufacturing an unproven product - but, who knows! It could be beneficial when you ingest a particle of gluten - not a great deal, but enough to damage your villi. My greatest concern is that the particle wouldn't come in contact with the enzyme.

I'm also concerned with their statement: "effectiveness is going to depend on the sensitivity of the person and the severity of the infraction." I think it's true that while some people are more noticably reactive - *all* celiacs are sensitive to minute amounts of gluten - and damage to the villi has been shown when only .1 gram of gluten has been ingested. Yikes!

I'm still interested in hearing what celiachap has to say about this though. Even when I am unbelievably careful, I sometimes (accidentally) get glutened. It's not enough to give me a GI response, but my emotional response is absolutely horrible. I would consider taking this enzyme before eating out or hell, maybe all the time - if it might help me to digest that microscopic amount of gluten that makes me crazy.

- Michelle :wub:

celiachap Apprentice
It could be beneficial when you ingest a particle of gluten - not a great deal, but enough to damage your villi.  My greatest concern is that the particle wouldn't come in contact with the enzyme. 

I would consider taking this enzyme before eating out or hell, maybe all the time - if it might help me to digest that microscopic amount of gluten that makes me crazy. 

- Michelle :wub:   

<{POST_SNAPBACK}>

That's exactly the way I feel about it. Even if DPP-IV only helps partially, as in the case of an accident, it's probably worth taking every day. Once I find out that I am OK with the DPP-IV, and (maybe) an associated multi-enzyme formula from Kirkman, I am going to take it on a daily basis. One of their multiple-enzyme products, Enzym-Complete, already has some DPP-IV included. They suggest augmenting that with the stand-alone DPP-IV (when needed). I think that the multi-formula has protease in it, which MAY be bad for celiacs to take.* Going on a regimen like this (provided it's safe) will hopefully improve the overall digestion process, and possibly protect against damage from accidental injestion due to contamination or restaurant errors. The fact that this company specializes in making products for patients that often have multiple allergies, intolerances, etc., is reassuring.

*Open Original Shared Link

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,188
    • Most Online (within 30 mins)
      7,748

    Leeila
    Newest Member
    Leeila
    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

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
×
×
  • Create New...