Gluten Cross-Reactivity UPDATE: How your body can still think you’re eating gluten even after giving it up.

March 13, 2013 in FAQ, FAQ, Foods in Moderation, Gut Health, The Autoimmune Protocol, The WHYs of the AIP

The Paleo Approach by Sarah BallantyneIn my research for The Paleo Approach, I feel that it is important to provide scientific references for every single statement I make.  This has me doing a great deal of fact checking, scouring the medical literature to verify information often gleaned from other paleo authors and bloggers.  Most of the time what I find out just helps reinforce concepts, filling in blanks, and typically making a strong case for my assertions.  But, every once in a while, I find information that makes me completely reevaluate a concept and sometimes even an aspect of the autoimmune protocol.

The update for this blog post comes from my further examination into the science behind gluten cross-reactivity.  While there are plenty of papers confirming how cross-reactive antibodies can be formed, I could not find any published studies confirming the results from Cyrex Labs (and my motto with the paper is if I can’t cite it, I don’t say it).  I contacted the company to request further information (I was particularly interested in the reported cross-reactivity to tapioca as I was trying to decide whether or not tapioca starch and/or pearls should be included in The Paleo Approach).  Cyrex labs responded quickly and informatively and my level of esteem for that company (which was high to begin with) elevated another couple of notches.  While they were unwilling to share proprietary data with me, they were able to point me to a recent publication that evaluated gluten cross-reactivity and share a summary of their proprietary findings (the paper did not show up on my PubMed searches).  As I devoured the paper (figuratively, not literally), I realized that an update to this post was required.  This is not an excerpt from The Paleo Approach but it is a direct result of my research for the book and much of the information that follows is still presented in it.

For those 20% of us with celiac disease or gluten-intolerance/sensitivity (whether diagnosed or not), it is critical to understand the concept of gluten cross-reactivity. Essentially, when your body creates antibodies against gluten, those same antibodies also recognize proteins in other foods. When you eat those foods, even though they don’t contain gluten, your body reacts as though they do. You can do a fantastic job of remaining completely gluten-free but still suffer all of the symptoms of gluten consumption—because your body still thinks you are eating gluten. This is a very important piece of information that I was missing until recently.

Proteins are made of long chains of amino acids (small proteins may only be 50 amino acids long whereas large proteins may be 2000 amino acids long) and it is the specific sequence of these amino acids that determines what kind of protein is formed. These amino acid chains are folded, kinked and buckled in extremely complex ways, which gives a protein its ‘structure’. This folding/structure is integral to the function of the protein.

An antibody is a Y shaped protein produced by immune cells in your body. Each tip of the Y contains the region of the antibody (called the paratope) that can bind to a specific sequence of amino acids (called the epitope) that are a part of the protein that the antibody recognizes/binds to (called the antigen). The classic analogy is that the antibody is like a lock and a 15-20 amino acid section of a protein/antigen is the key. There are 5 classes (or isotypes) of antibodies, each with distinctive functions in the body. The IgE class of antibodies are responsible for allergic reactions; for example, when someone goes into anaphylaxis after eating shellfish. The two classes IgG and IgA are critical for protecting us from invading pathogens but are also responsible for food sensitivities/intolerances. Both IgA and IgG antibodies are secreted by immune cells into the circulation, lymph, various fluids of the body (like saliva!) and tissues themselves. And both IgG and IgA antibodies are found in high concentrations in the tissues and fluids surrounding the gut (this is part of why the gut is considered our primary defense against infection).

The formation of antibodies against an antigen (whether this is an invading pathogen or a food) is an extremely complex process. When antibodies are being formed against a protein, the antibodies recognize specific (and short) sequences of amino acids in that protein. Depending on how the antigenic protein is folded, certain amino acid sequences in that protein are more likely to be the target of new antibody formation than others, simply because of the location of that sequence in the structure of the protein. Certain sequences of amino acids are more antigenic than others as well (i.e., more likely to stimulate antibody formation). This is also part of why certain foods have a higher potential to cause allergies and sensitivities.

Understanding that antibodies recognize short sequences of amino acids and not an entire protein is key to understanding the concept of cross-reactivity (and molecular mimicry, but that’s a topic for another post). It also is the reason why many different antibodies can be formed against one protein (this redundancy is important for protecting us from pathogens). Many different antibodies can also be formed against one pathogen or, more relevant to this discussion, one specific food.

So what happens in cross-reactivity? In this case the amino acid sequence that an antibody recognizes is also present in another protein from another food (in the case of molecular mimicry, that sequence is also present is a protein in the human body). There are only 20 different amino acids, so while there are millions of possible ways to link various amount of each amino acid together to form a protein, there are certain amino acid sequences that do tend to repeat in biology.

The take home message: depending on exactly what antibody or antibodies your body forms against gluten, it/they may or may not cross-react with other foods. So, not only are you sensitive to gluten, but your body now recognizes non-gluten containing foods as one and the same. Who needs to worry about this? Any of the estimated 20% of people who are gluten intolerant or have celiac disease, i.e., have formed antibodies against gluten.

A recent study evaluated the potential cross-reactivity of 24 food antigens.  These included:

  • Rye
  • Barley
  • Spelt
  • Polish Wheat
  • Oats (2 different cultivars)
  • Buckwheat
  • Sorghum
  • Millet
  • Amaranth
  • Quinoa
  • Corn
  • Rice
  • Potato
  • Hemp
  • Teff
  • Soy
  • Milk (Alpha-Casein, Beta-Casein, Casomorphin, Butyrophilin, Whey Protein and whole milk)
  • Chocolate
  • Yeast
  • Coffee (instant, latte, espresso, imported)
  • Sesame
  • Tapioca (a.k.a. cassava or yucca)
  • Eggs

They did not find cross-reactivity with all of these foods (as is implied by the Cyrex Labs gluten cross-reactivity blood test, a.k.a. Array 4).  But, they did find that their anti-gliadin antibodies (antibodies that recognize the protein fraction of gluten) did cross-react with all dairy including whole milk and isolated dairy proteins (casein, casomorphin, butyrophilin, and whey)—this may explain the high frequency of dairy sensitivities in celiac patients—oats, brewer/baker’s yeast, instant coffee (but not fresh coffee), milk chocolate (attributable to the dairy proteins in chocolate), sorghum, millet, corn, rice and potato.

While not all people with gluten sensitivities will also be sensitive to all of these foods, they should be highlighted as high risk for stimulating the immune system.   Just like trace amounts of gluten can cause a reaction in at least those with celiac disease (the threshold for a reaction has not been tested in non-celiac gluten sensitivity), even a small amount of these foods can perpetuate inflammation and immune responses. This is important when you think of the small amounts of corn used in so many foods and even the trace milk proteins that can be found in ghee.

Beyond this gluten contamination is common in the food supply and many grains and flours that are inherently gluten free may still contain gluten once processed.  Commonly contaminated grain products include millet, white rice flour, buckwheat flour, sorghum flour, and soy flour.  As these are commonly used ingredients in commercial gluten-free baked goods, extreme caution should be exercised.

Cyrex Labs offers a simple blood test that is referred to as their gluten ross-reactivity panel, a.k.a. Array 4.  It tests for reactions to the gluten cross-reactors mentioned above as well as the non cross-reactors evaluated in the paper.  Cyrex Labs reported to me that they see positive sensitivities frequently (many as high as 25%) in many of those foods in people with diagnosed gluten sensitivity.  This may reflect that when you have a leaky gut, food intolerances are quite easy to form.

If you have autoimmune disease (which has a very high correlation with gluten-sensitivity), celiac disease, gluten-sensitivity, or are simply not seeing the improvements you were hoping for by following a standard paleo diet, one or all of these foods may be the culprit. You have the choice of either cutting these foods out of your diet and seeing if you improve or get tested to see if your body produces antibodies against these foods.

When I first wrote this blog post, it made so many pieces of the puzzle come together.  I stopped eating chocolate (I had already given up coffee), fermented foods like sauerkraut and kombucha (because of the yeast content), eggs, and tapioca.  Over the months that followed, I was able to definitely discern that I am very sensitive to chocolate (perhaps because it is extremely high in phytic acid, discussed in this post) and eggs (discussed in this post).  I have successfully reintroduced fermented foods and have not been particularly inspired to test my sensitivity to tapioca (I test by eating a bit and seeing if I have a reaction, most typically my reactions are acne, but sometimes trouble sleeping, mood issues, joint aches, or increased itchiness and redness of my lichen planus lesions).  So, will I give coffee a try now?  Maybe, once in a while as a special treat, but removing gluten cross-reactivity from the list of ways coffee is suboptimal, really only removes one potential problem.  Coffee still has effects on cortisol and still correlates with increased inflammation.  Oh well.  Whether I can drink coffee again or not, I am glad to be able to share this updated information with all of you!

A great overview of proteins and antibodies (and source of protein folding image): http://publications.nigms.nih.gov/structlife/chapter1.html

A fairly technical review of food IgG-mediated food sensitivities: http://www.usbiotek.com/Downloads/information/criticalReview.pdf

Cyrex Labs Array 4: http://www.cyrexlabs.com/CyrexTestsArrays/tabid/136/Default.aspx

Image of antibody binding taken from http://classes.midlandstech.edu/carterp/Courses/bio225/chap17/ss2.htm

A. Vojdani and I. Tarash, “Cross-Reaction between Gliadin and Different Food and Tissue Antigens,” Food and Nutrition Sciences, Vol. 4 No. 1, 2013, pp. 20-32.  http://www.scirp.org/journal/PaperInformation.aspx?PaperID=26626

Thompson T et al. Gluten contamination of grains, seeds, and flours in the United States: a pilot study. J Am Diet Assoc. 2010 Jun;110(6):937-40. doi: 10.1016/j.jada.2010.03.014.

TPV Episode 17 Show Notes: Paleo 101

December 7, 2012 in Show Notes

Our seventeenth show!
Ep. 17: Paleo 101

In this episode, we hope to provide an overview of the paleo diet and help you navigate why the “rules” are the way they are. Why is it that we avoid grains? Beans? Sugar? What is inflammation and why are we trying so hard to avoid it? We hope we can take you by the hand and lead you through the reasoning. After this show, we hope you will be on a happy, healthy path for your life!

 

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The Paleo View (TPV), Episode 17: Paleo 101

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Why Aren’t Humans Adapted to Grains?

July 10, 2012 in FAQ, The WHYs Behind Paleo

A paleo diet is often presented as “eating the foods that humans evolved over 2.5 million years to eat for optimum health”.  I am guilty of presenting this explanation myself.  It’s an easy sound bite and resonates on an intuitive level for the scientifically-inclined.  However, this easy definition of the paleo diet renders the entire diet vulnerable to a common criticism.  While we claim that humans are not adapted to those foods that only became a part of our diet with the advent of agriculture, (specifically grains, legumes and dairy), many refute this claim (and provide scientific evidence of adaptations!).  While the sometimes vehement debates over the merits of a paleo diet are moot to most of us (we know it works for us and that’s enough!), this criticism of what many people think of as a cornerstone of the paleo diet is absolutely valid.

The speed in which a species adapts to a change in environment (which might include anything from predators, to weather, to food sources) depends on something called evolutionary pressure.  Any factors that reduce reproductive success in a proportion of a population influence the genetics of that population–this is evolutionary pressure.  This pressure “selects” for certain genetic traits that increase survival of the species.  Survival, in this case, means health of the individual sufficient to reproduce.  What happens after reproduction doesn’t exert pressure for genetic adaptation. 

The period of time since the advent of agriculture is fairly short in terms of the length of time that humans have been evolving; however, it is absolutely enough time to adapt given sufficient evolutionary pressure.  Dairy consumption is an excellent example of a way in which humans (at least a proportion of them) have adapted to a new food source over a short period of time.  Lactose tolerance and lactose persistence (ability to still digest lactose as an adult) is present in 80% of humans of European and American descent, which means that 80% of European and American individuals contain the genes for the enzyme lactase.  These people are descendants of lines in which adaptation has occurred (in conjunction with dairy consumption, which might be why this adaptation has not occurred to such a high degree in other cultures) 1.  If humans continue to consume dairy products, the percentage of people who contain the gene for lactase will gradually increase until everyone is lactose tolerant and lactose persistent.  Dairy may still not be an optimal food (casein is highly allergenic; milk contains protease inhibitors), but this adaptation is the chief reason why the exclusion of dairy from the paleo diet is so contentious (especially when considering raw, grass-fed dairy).  Indeed, the scientific literature is divided between studies showing that milk is beneficial for our health versus detrimental for our health (for a great summary of this argument see http://chriskresser.com/dairy-food-of-the-gods-or-neolithic-agent-of-disease).

The same process of adaptation is happening as we speak with regards to grains.  For example, since the advent of agriculture, humans have increased the number copies of the genes for salivary amylase, the enzyme in our saliva that starts the digestion of starch as we eat 2.  However, the scientific literature has more conclusively established a link between the dietary lectins found in grains, especially gluten, and a huge variety of health conditions (see The Paleo Answer).  The incidence of celiac disease and gluten-sensitivity is increasing (and some studies predict that they are still very underdiagnosed) 3,4.  There is a growing body of scientific literature linking gluten sensitivity to autoimmune disease 5,6Yes, there is genetic adaptation, but human health is still indisputably negatively affected by consumption of grains.  Gluten likely causes the telltale damage to the gut lining seen in celiac disease at least to some degree in most individuals (obviously, there is huge variability here).  Once study author wrote “If you look for coeliac disease you will find it” 4

It’s not that humans haven’t adapted to eating grains; it’s that humans haven’t fully adapted to eating grains. Evolutionary pressure is relatively low because the health effects of grain consumption doesn’t change reproduction rates dramatically.  However, it is very likely that there are people out there who are carrying a set of genetics that does make them adapted to eating grains.  This is why when someone tells me that they are completely healthy no matter what they eat, I simply congratulate them.  They may be adapted to Neolithic foods (they might also be even healthier on a paleo diet, but they aren’t likely to try it if they feel so great now, so I don’t belabor the point).  And, given enough time, humans will adapt to eating grains and will eventually thrive on its consumption.  But you are not going to change your genetics.  If you are part of the majority of humans who do not carry complete genetic adaptations to grain consumption, you are better off without it.  Depending on where you are in the spectrum, you may never be able to tolerate even small amounts or you may be able to incorporate regular cheat meals into your diet with little harm. 

The answer to this question is not straight forward.  10,000 years is insufficient time for humans to have fully adapted to thisnew food source.  Basically, humans are adapting but are not yet fully adapted.  So, you get to choose.  Do you want to eat a diet that you are not fully adapted to in the hopes that your genes will contribute to the eventual complete adaptation of our species to this diet?  Or do you want to live the healthiest life you can now?

1 Enattah N et al. “Evidence of Still-Ongoing Convergence Evolution of the Lactase Persistence T-13910 Alleles in Humans”. The American Journal of Human Genetics  2007. 81(3): 615–25.

2 Wilson, David S. (1994). “Adaptive genetic variation and human evolutionary psychology”. Ethology and Sociobiology 15 (4): 219–35. DOI:10.1016/0162-3095(94)90015-9.

3 Caproni M, et al. Celiac disease and dermatologic manifestations: many skin clue to unfold gluten-sensitive enteropathy.  Gastroenterol Res Pract. 2012;2012:952753. Epub 2012 May 30.

4 Aziz I, Sanders DS. Are we diagnosing too many people with coeliac disease? Proc Nutr Soc. 2012 May 3:1-7. [Epub ahead of print]

5 Fasano A. Zonulin, regulation of tight junctions, and autoimmune diseases. Ann N Y Acad Sci. 2012 Jul;1258(1):25-33.

64 Korponay-Szabó IR et al. Gluten-dependent intestinal autoimmune response. Curr Pharm Des. 2012 Jun 21. [Epub ahead of print]