Gluten immunochemistry
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
The immunochemistry of Triticeae glutens is important in several inflammatory diseases. It can be subdivided into innate responses (direct stimulation of immune system), class II mediated presentation (HLA DQ), class I meditiated stimulation of killer cells, and antibody recognition. The responses to gluten proteins and polypeptide regions differs according to the type of gluten sensitivity. The response is also dependent on the genetic makeup of the human leukocyte antigen genes. In gluten sensitive enteropathy, there are 4 types of recognition, innate immunity (a form of cellular immunity priming), HLA-DQ, and antibody recognition of gliadin and transglutaminase. With idiopathic gluten sensitivity only antibody recognition to gliadin has been resolved. In wheat allergy, the response pathways are mediated through IgE against other wheat proteins and other forms of gliadin.
Innate immunity
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Innate immunity to gluten refers to an immune response primer that works independently of T-cell receptor or antibody recognition of the 'innate' peptide. This peptide acts directly on cells, such as monocytes, stimulating their growth and differentiation.[1] Innate immunity to gluten is complicated by an apparent role gluten has in bypassing normal host defense and peptide exclusion mechanisms in the gut. While not truly innate, these activities allow gliadin to enter into areas where many lymphocytes patron. In bypassing these filters gliadin alter the normal behavior of both digestive cells, called enterocytes or epithelial cells, and lymphocytes. This increases the potential of causing sensitivity (see Underlying Conditions). One potential explanation of why certain people become sensitive is that these individuals may not produce adequate peptidases in some areas of the gut, allowing these peptides to survive. Other explanation for some may be that food chemicals or drugs are weakening the defenses. This can be the case with ω5-gliadin allergy with salicylate sensitivity. There is no clear reasoning, either from genetics or from long term studies of susceptible individuals why these gut peptide restrictions would change.
Once inside, α-9 gliadin 31-55 shows the ability to activate undifferentiated immune cells that then proliferate and also produce inflammatory hormones notably Interleukin 15. This produces a number of downstream responses that are pro-inflammatory. The other peptide that may have innate behavior is the "CXCR3" receptor binding peptides, the receptor exists on enterocytes, the brush border membrane cells. The peptide displaces an immune factor and signals the disruption of the membrane seal, the tight junctions, between cells.
Alpha gliadin 31-43
Gluten bears an innate response peptide (IRP) found on α-9 gliadin, at positions 31-43 and on α-3, 4, 5, 8, and 11 gliadins. The IRP lies within at 25 amino-acid long region that is resistent to pancreatic proteases. The 25mer is also resistent to brush border membrane peptidases of the small intestine in coeliacs.[3] IRP induced the rapid expression of interleukin 15 (IL15) and other factors.[4] Thus IRP activates the immune system.[5][1] Studies show that, while in normal individuals the peptide is trimmed over time to produce inactive peptide, in celiacs a 19mer may loose a residue from one end or the other, after prolonged incubation that 50% remains intact.
Intraepithileal lymphocytes and IL15
The release of IL15 is a major factor in coeliac disease as IL15 has been found to attract intraepithelial lymphocytes (IEL) that characterize Marsh grade 1 and 2 coeliac disease.[6] Lymphocytes attracted by IL-15 are composed of markers enriched on natural killer cells versus normal helper T-cells. One hypothesis is that IL-15 induces the highly inflammatory Th1 response that activates T-helper cells (DQ2 restricted gliadin specific) that then orchestrate the destructive response, but the reason why inflammatory cells develope prior to gliadin specific helper cells is not known.[7] The IRP response differs from typical responses that stimulate IL15 release, such as viral infection. In addition, other cytokines such as IL12 and IL2, which are typically associated with T-helper cell stimulation, are not involved. In these two ways the innate peptide activation of T-cells in celiac disease is strange. IL-15 appears to induce increases in MICA and NKG2D that may increase brush-border cell killing.[1]
In addition, innate immunity to IRP peptide is involved in coeliac disease, dermatitis herpetiformis and possibly juvenile diabetes. IRP targets monocytes and increases the production of IL-15 by an HLA-DQ independent pathway, a subsequent study showed the both this region and the "33mer" could create the same response, in cells from both treated coeliacs and non-coeliacs. However, unlike the non-coeliacs, the treated coeliac cells produce the disease marker nitrite.[8] This indicates that another abnormality in people with coeliac disease that allows stimulation to proceed past the normal healthy state. After extensive study, there is no known genetic association for this that appears to stand out at present, and implicates other environmental factors in the defect.
Infiltrating peptides
Some alpha gliadin have other direct-acting properties. Other gliadin peptides, one in a glutamine rich region and another peptide, "QVLQQSTYQLLQELCCQHLW", bind a chemoattractant receptor, CXCR3. Gliadin binds to, blocks and displaces a factor, I-TAC, that binds this receptor.[2] In the process it recruits more CXCR3 receptor, increases MyD88 and Zonulin expression.[1][9] The factor it displaces, I-TAC, is a T-cell attractant. This peptide may also be involved in increased risk for type 1 diabetes as zonulin production is also a factor.[10] This triggering of zonulin ultimately results in the degradation of tight junctions allowing large solutes, such as proteolytic resistent gliadin fragments to enter behind the brush border membrane cells.
One study examined the effect of ω-5 gliadin, the primary cause of WD-EIA, and found increased permeability of intestinal cells.[11] Other studies show that IgE reactivity to ω-5 gliadin increases greatly when deamidated or crosslinked to transglutaminase.[12]
HLA Class I restrictions to gliadin
HLA class I restrictions to gliadin are not well characterized. HLA-A2 presentation has been investigated. The HLA-A antigens can mediate apoptosis in autoimmune disease and HLA A*0201 in with the HLA-DQ8 haplotypes has been documented[13]. The class I sites were found on the carboxyl end of gliadin at positions 123-131, 144-152, and 172-180. The involvement of class I responses may be minor, since antibodies to transglutaminase correlate with pathogenesis and recognition of extracellular matrix and cell surface transglutaminase can explain the destruction within coeliac disease. This process involves antibody-dependent cellular cytotoxicity. With regard to a recpetor called FOS, euphemistically called the "Death Receptor", enterocytes appear to overexpress the recept in coeliac leasions, there is speculation that Class I presentation of glaidin, tTG or other peptides that invokes signalling. The role of class I receptor in cell-mediated programmed cell (enterocyte) death is not known.
MIC
These proteins are called MHC class I polypeptide-related sequence A and B. Discovered by sequence homology analysis these proteins are found on the surface of enterocytes of the small intestine, are are believed to play a role in disease. Studies to date have revealed no mutation that would increase risk for MICA.
HLA-DQ recognition of gluten
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| Illustration of HLA-DQ with peptide in the binding pocket | HLA DQ Receptor with bound peptide and TCR |
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HLA-DQ proteins present polypeptide regions of proteins of about 9 amino acids and larger in size (10 to 14 residues in involved in binding is common for gliadin) to T lymphocytes.[16] Gliadin proteins can be adsorbed by APC. After digestion in the lysozomes of APCs, glaidin peptides can be recycled to the cell's surface bound to DQ, or they can be bound and presented directly from the cell surface.[17] The major source of inflammatory gluten is dietary gluten. Optimal reactivity of gliadin occurs when the protein is partially digested by small intestinal lysozyme and trypsin into proteolytic digests. These polypeptides of gluten can then make their way behind the epithelial layer of cells (membrane), where APCs and T-cells reside in the lamina propria. (See: Underlying conditions)
The APC bearing DQ-gliadin peptide on the surface can bind to T-cells that have an antibody-like T-cell receptor the specifically recognized DQ2.5 with gliadin. The complex (APC-DQ-glaidin) thus stimulates the gliadin specific T-cells to divide. These cells cause B-cells that recognize gliadin to proliferate. The B-cells mature into plasma cells producing anti-gliadin antibodies. This does not cause coeliac disease and is an unknown factor in idiopathic disease. Enteropathy is believed to occur when tissue transglutaminase(tTG) covelantly links itself to gliadin peptides that enter the lamina propria of the intestinal villus. The resulting structure can be presented by APC (with the same gliadin recognizing DQ isoforms) to T-cells, and B-cells can produce anti-transglutaminase antibodies. This appears to result in the destruction of the villi. The release of gliadin by transglutaminase does not lessen disease. When tTG-gliadin undergoes hydrolysis (steals a water to cut the two apart), the result is deamidated gliadin. Deamidated gliadin peptides are more inflammatory relative to natural peptides. Deamidated gliadin is also found in foods that have added gluten, such as wheat bread, food pastes.
The major gluten proteins that are involved in coeliac disease are the α-gliadin isoforms. Alpha gliadin is composed of repeated motifs that, when digested, can be presented by HLA-DQ molecules. DQ2.5 recognizes several motifs in gluten proteins, and therefore HLA-DQ can recognize many motifs on each gliadin (see Understanding DQ haplotypes and DQ isoforms on the right)[18] However, numbers of different proteins from the grass tribe Triticeae have been found to carry motifs presented by HLA DQ2.5 and DQ8. Wheat has a large number of these proteins because its genome contains chromosomes derived from two goat grass species and a primitive wheat species.[19][20] The positions of these motifs in different species, strains and isoforms may vary because of insertions and deletions in sequence. There are a large number of wheat variants, and a large number of gliadins in each variant, and thus many potential sites. These proteins once identified and sequenced can be surveyed by sequence homology searches.
HLA-DQ2.5
HLA-DQ recognition of gliadin is critical to the pathogenesis of gluten-sensitive enteropathy, it also appears to be involved in idiopathic gluten sensitivity (See:Understanding DQ Haplotypes and DQ isoforms on the right).
HLA-DQ2 primarily presents gliadins with the HLA-DQ isoform DQ2.5 (DQ α5-β2) isoform. DQA1*0202:DQB1*0201 homozygotes (DQ α2-β2) also appear to be able to present pathogenic gliadin peptides, but a smaller set with lower binding affinity.
DQ2.5 and α-gliadin
Many of these gliadin motifs are substrates for tissue transglutaminase and therefore can be modified by deamidation in the gut to create more inflammatory peptides. The most important recognition appears to be directed toward the α-/β-gliadins. An example of the repetition of a motif across many proteins, the α-2 gliadin (57-68) and (62-75) are also found on α-4, α-9 gliadin.[22] Many gliadins contain the "α-20 motif", which is found in wheat and other Triticeae genera.(see also: "α-20" gliadin motifs). Alpha-2 secalin, the glutinous protein in rye, is composed of two amino-terminal overlapping T-cell sites at positions (8-19) and (13-23).[22]
A2-gliadin
Although T-cell responses to many prolamins can be found be found in coeliac disease, one particular gliadin, α2-gliadin appears to be the focus of T-cells.[24] These responses were dependent on prior treatment with tissue transglutaminase. Α2-gliadin differs from the other α-gliadins, specifically because it contains an insert of 14 amino acids[25]. This particular insertion creates 6 T-cell sites where, in the most similar gliadins, there are 2 or less sites. The sites belong to three epitope groups "α-I", "α-II", and "α-III"[26] The insertion also creates a larger region of α-gliadin that is resistant to gastrointestinal proteases. The smallest digest of trypsin and chymotrypsin for the region is a 33mer. This particular region has three tissue transglutaminase sites, two sites that lie within the 14 amino acid insertion, a region of maximal stimulation are found with more than 80% reduction in response for native, un-deaminated, sequence at the position.[27] Because of the density of T-cell sites on the "33mer" the affinity for deamidated gliadin is strongly indicates that it may be best treated as a single T-cell site of much higher affinity.[17] This site alone may fulfill all the T-helper cell adaptive immune requirements with HLA-DQ2.5 involvement in some coeliac disease.
DQ2.5 and γ-gliadin
While gamma glaidin is not as important to DQ2.5 mediated disease as α-2 gliadin there are a number of identified motifs. The gamma epitopes identified are DQ2-"γ-I", -"γ-II" (γ30), -"γ-III", -"γ-IV", -"γ-VI" and -"γ-VII" [28][29] Some of these epitopes are recognized in children who do not have T-cell reactivities toward α-2 gliadin.[30] A 26 residue proteolytic resistance fragment has been found on γ-5 gliadin, positions 26–51, that has multiple transglutaminase and T-cell epitopes. This site has 5 overlapping T-cells sites of DQ2-"γ-II", -"γ-III", -"γ-IV", and "γ-glia 2".[31] Computer analysis of 156 prolamins and glutelins revealed many more resistent fragments, one , a γ-gliadin, containing 4 epitopes was 68 amino acids in length.
DQ2 and glutelins
Triticeae glutelins presented by DQ2 is some coeliacs. In wheat, the low molecular weight glutenins often share structural similarity with the prolamins of the similar species of Triticeae. Two motifs, K1-like (46-60), pGH3-like (41-59) and GF1(33-51) have been identified. High molecular weight glutenin has also been identified as a potentially toxic protein[32] Some of the HMW glutenins increase response with transglutaminase treatment, indicating the sites might be similar to alpha-gliadin and gamma gliadin T-cell sites.[33]
DQ2.2 restricted gliadin sites
DQ2.2 can present a fewer number of lower affinity sites relative to DQ2.5. Some of these sites are found on γ-gliadin the gliadin most similar to prolamins of other Triticeae genera, a gliadin that appears to similar to ancestral. Antigen presenting cells bearing DQ2.2 can present alpha gliadin sites, for example alpha-II region of the "33mer" and therefore the "33mer" may have a role in DQ2.2 bearing individuals, but the binding capacity is substantially lower.[29]
HLA-DQ8
HLA-DQ8 confers susceptibility to coeliac disease but in a fashion somewhat similar to DQ2.5.[34] Homozygotes of DQ8, DQ2.5/DQ8 and DQ8/DQ2.2 are higher than expected based on levels in the general population.(see: Understanding DQ haplotypes and DQ isoforms).[15] HLA-DQ8 is generally not as involved in the most severe complications, and it does not recognize the "33mer" of α-2 gliadin to the same degree as DQ2.5. There are a smaller number of gliadin (prolamin) peptides presented by HLA-DQ8. A few studies have been done on the adaptive immune response for DQ8/DQ2- individuals. DQ8 appears to rely much more on adaptive immunity to the carboxyl half of alpha gliadins.[35]. In addition, it appear to react with gamma gliadin to a degree comparable to DQ2.5.[36] T-cell responses to the high molecular weight glutenin may be more important with DQ8 mediated than DQ2.5 mediated celiac disease.[32]
Antibody recognition
Antibody recognition of gluten is complex. Direct binding to gluten such as anti-gliadin antibodies has an ambiguous pathogenesis in coeliac disease. The crosslinking of gliadin with tissue transglutaminase leads to the production of anti-transglutaminase antibodies, but this is mediated through T-cell recognition of gliadin. The allergic recognition of gliadin by mast cells, eosinophiles in the presence of IgE has notable direct consequences, such as exercise-induced anaphylaxis.
Anti-gliadin antibodies, like those detected in celiac disease bind to the α-2 gliadin(57-73).[37] This site is within the T-cell reactive "33mer" presented by DQ2.5. There has been some suggestion wheat plays a role in juvenile diabetes as antibodies to the non-glutinous seed storage glb-1 (a globulin) are implicated in crossreactive autoantigenic antibodies that destroy islet cells in the pancreas.[38] Anti-gliadin antibodies have been found to synapsin I[39] Omega-gliadin and the HMW Glutenin subunit antibodies have been found most commonly in individuals with exercise-induced anaphylaxis and Baker's allergy, and represent a potent class of gluten allergens. Non-glutinous proteins in wheat are also allergens, these include: LTP (albumin/globulin), thioredoxin-hB, and wheat flour peroxidase.[40][41][42][43] A particular 5 residue peptide, Gln-Gln-Gln-Pro-Pro motif, has been found to be a major wheat allergen. [44]
Taming Triticeae Immunochemistry
New immunogenic motifs appear in the literature almost monthly and new gliadin and Triticeae protein sequences appear that contain these motifs. The HLA DQ2.5 restricted peptide "I I Q P Q Q P A Q" produced approximately 50 hits of identical sequences in NCBI-Blast search is one of a several dozen known motifs[22] whereas only a small fraction of Triticeae gluten variants have been examined. For this reason the immunochemisty is best discussed at the level of Triticeae, because it is clear that the special immunological properties of the proteins appear to have basal affinities to this taxa, appearing concentrated in wheat as a result of its three various genomes. Some current studies claim that removing the toxicity of gliadins from wheat as plausbile,[45] but, as the above illustrates, the problem is monumental. There are many gluten proteins, 3 genomes with many genes each for alpha, gamma, and omega gliadins. For each motif many genome-loci are present, and there are many motifs, some still not known. Different strains of triticeae exist for different industrial applications; durum for pasta and food pastes, 2 types of barley for beer, bread wheats used in different areas with different growing conditions. Replacing these motifs is not a plausible task since a contamination of 0.02% wheat in a GF diet is considered to be pathogenic and would require replacing motifs in all known regional varieties, potentially 1000s of genetic modifications.[45] Class I and Antibody responses are downstream of Class II recognition and are of little remedial value in change. The innate response peptide could be a silver bullet, assuming there is only one of these per protein and only a few genome loci with the protein. The bigger question is why late onset gluten sensitivity rapidly rising, is this truly a wheat problem or is it something that being done to wheat, or to those who are eating wheat (for example communicable diseases as trigger)? Some individuals are susceptible by genetics (early onset), but many late onset cases could have variable triggers because there is nothing genetically that separates the 30 to 40% of caucasians that could have Triticeae senstivity from the ~1% that, in their lifetime, will have some level of this disease. Another strategy in making wheat less immunogenic is to insert proteolytic sites in the longer motifs (25-mer and 33-mer) facilitating more complete digestion.
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 van Heel DA, West J (2006). "Recent advances in coeliac disease". Gut. 55 (7): 1037–46. doi:10.1136/gut.2005.075119. PMID 16766754. Unknown parameter
|month=ignored (help) - ↑ 2.0 2.1 Lammers KM, Lu R, Brownley J; et al. (2008). "Gliadin induces an increase in intestinal permeability and zonulin release by binding to the chemokine receptor CXCR3". Gastroenterology. 135 (1): 194–204.e3. doi:10.1053/j.gastro.2008.03.023. PMID 18485912. Unknown parameter
|month=ignored (help) - ↑ Mamone G, Ferranti P, Rossi M; et al. (2007). "Identification of a peptide from alpha-gliadin resistant to digestive enzymes: implications for celiac disease". J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 855 (2): 236–41. doi:10.1016/j.jchromb.2007.05.009. PMID 17544966. Unknown parameter
|month=ignored (help) - ↑ The other factors are (COX-2, CD25, p38 MAP kinase activation by CD3 negative cells (Lamina proxima mononuclear cells) and CD83 on dendritic cells
- ↑ Maiuri L, Ciacci C, Ricciardelli I, Vacca L, Raia V, Auricchio S, Picard J, Osman M, Quaratino S and Londei M. (2003). "Association between innate response to gliadin and activation of pathogenic T cells in coeliac disease". Lancet. 362 (9377): 30–37. doi:10.1016/S0140-6736(03)13803-2. PMID 12853196.
- ↑ Maiuri L, Ciacci C, Vacca L; et al. (2001). "IL-15 drives the specific migration of CD94+ and TCR-gammadelta+ intraepithelial lymphocytes in organ cultures of treated celiac patients". Am. J. Gastroenterol. 96 (1): 150–6. PMID 11197245. Unknown parameter
|month=ignored (help) - ↑ Londei M, Ciacci C, Ricciardelli I, Vacca L, Quaratino S, Maiuri L (2005). "Gliadin as a stimulator of innate responses in celiac disease". Mol. Immunol. 42 (8): 913–8. doi:10.1016/j.molimm.2004.12.005. PMID 15829281. Unknown parameter
|month=ignored (help) - ↑ Bernardo D, Garrote JA, Fernández-Salazar L, Riestra S, Arranz E (2007). "Is gliadin really safe for non-coeliac individuals? Production of interleukin 15 in biopsy culture from non-coeliac individuals challenged with gliadin peptides". Gut. 56 (6): 889–90. doi:10.1136/gut.2006.118265. PMID 17519496.
- ↑ Thomas KE, Sapone A, Fasano A, Vogel SN (2006). "Gliadin stimulation of murine macrophage inflammatory gene expression and intestinal permeability are MyD88-dependent: role of the innate immune response in Celiac disease". J. Immunol. 176 (4): 2512–21. PMID 16456012. Unknown parameter
|month=ignored (help) - ↑ Sapone A, de Magistris L, Pietzak M; et al. (2006). "Zonulin upregulation is associated with increased gut permeability in subjects with type 1 diabetes and their relatives". Diabetes. 55 (5): 1443–9. PMID 16644703. Unknown parameter
|month=ignored (help) - ↑ Bodinier M, Legoux MA, Pineau F; et al. (2007). "Intestinal translocation capabilities of wheat allergens using the Caco-2 cell line". J. Agric. Food Chem. 55 (11): 4576–83. doi:10.1021/jf070187e. PMID 17477542. Unknown parameter
|month=ignored (help) - ↑ Palosuo K, Varjonen E, Nurkkala J; et al. (2003). "Transglutaminase-mediated cross-linking of a peptic fraction of omega-5 gliadin enhances IgE reactivity in wheat-dependent, exercise-induced anaphylaxis". J. Allergy Clin. Immunol. 111 (6): 1386–92. PMID 12789243. Unknown parameter
|month=ignored (help) - ↑ Gianfrani C, Troncone R, Mugione P, Cosentini E, De Pascale M, Faruolo C, Senger S, Terrazzano G, Southwood S, Auricchio S, Sette A (2003). "Celiac disease association with CD8+ T cell responses: identification of a novel gliadin-derived HLA-A2-restricted epitope". J Immunol. 170 (5): 2719–26. PMID 12594302.
- ↑ van Belzen MJ, Koeleman BP, Crusius JB; et al. (2004). "Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients". Genes Immun. 5 (3): 215–20. doi:10.1038/sj.gene.6364061. PMID 15014431. Unknown parameter
|month=ignored (help) - ↑ 15.0 15.1 Karell K, Louka AS, Moodie SJ; et al. (2003). "HLA types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac Disease". Hum. Immunol. 64 (4): 469–77. PMID 12651074. Unknown parameter
|month=ignored (help) - ↑ van de Wal Y, Kooy YM, Drijfhout JW, Amons R, Koning F (1996). "Peptide binding characteristics of the coeliac disease-associated DQ(alpha1*0501, beta1*0201) molecule". Immunogenetics. 44 (4): 246–53. PMID 8753854.
- ↑ 17.0 17.1 Qiao SW, Bergseng E, Molberg O, Xia J, Fleckenstein B, Khosla C, and Sollid LM. (2004). "Antigen presentation to celiac lesion-derived T cells of a 33-mer gliadin peptide naturally formed by gastrointestinal digestion". J Immunol. 173 (3): 1756–1762. PMID 15265905.
- ↑ McLachlan A, Cullis PG, Cornell HJ (2002). "The use of extended amino acid motifs for focussing on toxic peptides in coeliac disease". J. Biochem. Mol. Biol. Biophys. 6 (5): 319–24. doi:10.1080/1025814021000003238. PMID 12385967. Unknown parameter
|month=ignored (help) - ↑ >Heun M, Schäfer-Pregl R, Klawan D, Castagna R, Accerbi M, Borghi B, and Salamini F (1997). "Site of Einkorn Wheat Domestication Identified by DNA Fingerprinting". Science. 278 (5341): 1312–1314. doi:10.1126/science.278.5341.1312.
- ↑ Dvorak J, Akhunov ED, Akhunov AR, Deal KR, and Luo MC (2006). "Molecular characterization of a diagnostic DNA marker for domesticated tetraploid wheat provides evidence for gene flow from wild tetraploid wheat to hexaploid wheat". Mol Biol Evol. 23 (7): 1386–1396. doi:10.1093/molbev/msl004. PMID 16675504.
- ↑ Kim C, Quarsten H, Bergseng E, Khosla C, Sollid L (2004). "Structural basis for HLA-DQ2-mediated presentation of gluten epitopes in celiac disease". Proc Natl Acad Sci U S A. 101 (12): 4175–9. doi:10.1073/pnas.0306885101. PMID 15020763. PMC 384714
- ↑ 22.0 22.1 22.2 Vader L, Stepniak D, Bunnik E, Kooy Y, de Haan W, Drijfhout J, Van Veelen P, Koning F (2003). "Characterization of cereal toxicity for celiac disease patients based on protein homology in grains". Gastroenterology. 125 (4): 1105–13. doi:10.1016/S0016-5085(03)01204-6. PMID 14517794.
- ↑ Qiao SW, Bergseng E, Molberg Ø; et al. (2004). "Antigen presentation to celiac lesion-derived T cells of a 33-mer gliadin peptide naturally formed by gastrointestinal digestion". J. Immunol. 173 (3): 1757–62. PMID 15265905. Unknown parameter
|month=ignored (help) - ↑ Arentz-Hansen H, Körner R, Molberg O; et al. (2000). "The intestinal T cell response to alpha-gliadin in adult celiac disease is focused on a single deamidated glutamine targeted by tissue transglutaminase". J. Exp. Med. 191 (4): 603–12. PMC 2195837. PMID 10684852. Unknown parameter
|month=ignored (help) - ↑ The sequence of the insert is P-Q-P-Q-L-P-Y-P-Q-P-Q-L-P-Y Template:Pubmed
- ↑ 1 "α-I" site, 3 "α-II" sites, and 2 "α-III" sites, Template:Pubmed
- ↑ Anderson RP, van Heel DA, Tye-Din JA, Jewell DP, Hill AV (2006). "Antagonists and non-toxic variants of the dominant wheat gliadin T cell epitope in coeliac disease". Gut. 55 (4): 485–91. doi:10.1136/gut.2005.064550. PMID 16299041. Unknown parameter
|month=ignored (help) - ↑ lim"γ-II" = IQPEQPAQL, lim"γ-III" = EQPEQPYPE, lim"γ-IV" = SQEFPQPEQ, "γ-VI" = PEQPFPEQPEQ and lim"γ-VII" = PQPQQQFPQ are derived from pubmed 15972656
- ↑ 29.0 29.1 Qiao SW, Bergseng E, Molberg O, Jung G, Fleckenstein B, Sollid LM (2005). "Refining the rules of gliadin T cell epitope binding to the disease-associated DQ2 molecule in celiac disease: importance of proline spacing and glutamine deamidation". J. Immunol. 175 (1): 254–61. PMID 15972656. Unknown parameter
|month=ignored (help) - ↑ Vader W, Kooy Y, Van Veelen P; et al. (2002). "The gluten response in children with celiac disease is directed toward multiple gliadin and glutenin peptides". Gastroenterology. 122 (7): 1729–37. PMID 12055577. Unknown parameter
|month=ignored (help) - ↑ Shan L, Qiao SW, Arentz-Hansen H; et al. (2005). "Identification and analysis of multivalent proteolytically resistant peptides from gluten: implications for celiac sprue". J. Proteome Res. 4 (5): 1732–41. doi:10.1021/pr050173t. PMC 1343496. PMID 16212427.
- ↑ 32.0 32.1 Dewar D, Amato M, Ellis H, Pollock E, Gonzalez-Cinca N, Wieser H, Ciclitira P (2006). "The toxicity of high molecular weight glutenin subunits of wheat to patients with coeliac disease". Eur J Gastroenterol Hepatol. 18 (5): 483–91. doi:10.1097/00042737-200605000-00005. PMID 16607142.
- ↑ Molberg Ø, Solheim Flaete N, Jensen T; et al. (2003). "Intestinal T-cell responses to high-molecular-weight glutenins in celiac disease". Gastroenterology. 125 (2): 337–44. PMID 12891534. Unknown parameter
|month=ignored (help) - ↑ HLA-DQ8 generally refers to DQ8.1, DQA1*0301:DQB1*0302 but DQA1*0301 and DQA1*0303 can produce the same functional isoform, rarely DQA1*0503 is in the DQ8 haplotype, it has no known association with disease
- ↑ positions (~230-240) and (>241-<255) of alpha gliadin AJ133612
- ↑ For γ-gliadins, γ-M369999 gliadin, reaction occurs at multiple sites (position: (~16-24), (>41-<60), (~79-90), (~94-102), (>101-<120))
- ↑ Bateman EA, Ferry BL, Hall A, Misbah SA, Anderson R, and Kelleher P. (2004). "IgA antibodies of coeliac disease patients recognise a dominant T cell epitope of A-gliadin". Gut. 53 (9): 1274–1278. doi:10.1136/gut.2003.032755. PMID 15306584.
- ↑ MacFarlane AJ, Burghardt KM, Kelly J, Simell T, Simell O, Altosaar I, and Scott FW. (2003). "A type 1 diabetes-related protein from wheat (Triticum aestivum). cDNA clone of a wheat storage globulin, Glb1, linked to islet damage". J Biol Chem. 278 (1): 54–63. doi:10.1074/jbc.M210636200. PMID 12409286.
- ↑ Alaedini A, Okamoto H, Briani C; et al. (2007). "Immune cross-reactivity in celiac disease: anti-gliadin antibodies bind to neuronal synapsin I". J. Immunol. 178 (10): 6590–5. PMID 17475890.
- ↑ Pastorello EA, Farioli L, Conti A; et al. (2007). "Wheat IgE-Mediated Food Allergy in European Patients: alpha-Amylase Inhibitors, Lipid Transfer Proteins and Low-Molecular-Weight Glutenins. Allergenic Molecules Recognized by Double-Blind, Placebo-Controlled Food Challenge". 144 (1): 10–22. doi:10.1159/000102609. PMID 17496422.
- ↑ Gómez L, Martín E, Hernández D; et al. (1990). "Members of the alpha-amylase inhibitors family from wheat endosperm are major allergens associated with baker's asthma". FEBS Lett. 261 (1): 85–8. PMID 2307238.
- ↑ Weichel M, Glaser AG, Ballmer-Weber BK, Schmid-Grendelmeier P, Crameri R (2006). "Wheat and maize thioredoxins: a novel cross-reactive cereal allergen family related to baker's asthma". J. Allergy Clin. Immunol. 117 (3): 676–81. doi:10.1016/j.jaci.2005.11.040. PMID 16522470.
- ↑ Sánchez-Monge R, García-Casado G, López-Otín C, Armentia A, Salcedo G (1997). "Wheat flour peroxidase is a prominent allergen associated with baker's asthma". Clin. Exp. Allergy. 27 (10): 1130–7. PMID 9383252.
- ↑ Tanabe S, Arai S, Yanagihara Y, Mita H, Takahashi K, Watanabe M (1996). "A major wheat allergen has a Gln-Gln-Gln-Pro-Pro motif identified as an IgE-binding epitope". Biochem. Biophys. Res. Commun. 219 (2): 290–3. doi:10.1006/bbrc.1996.0225. PMID 8604979.
- ↑ 45.0 45.1 Benahmed M, Mention J, Matysiak-Budnik T, Cerf-Bensussan N (2003). "Celiac disease: a future without gluten-free diet??". Gastroenterology. 125 (4): 1264–7. doi:10.1016/j.gastro.2003.07.002. PMID 14517809.