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. 1996 Jun;64(6):2031–2040. doi: 10.1128/iai.64.6.2031-2040.1996

Potential role of molecular mimicry between Helicobacter pylori lipopolysaccharide and host Lewis blood group antigens in autoimmunity.

B J Appelmelk 1, I Simoons-Smit 1, R Negrini 1, A P Moran 1, G O Aspinall 1, J G Forte 1, T De Vries 1, H Quan 1, T Verboom 1, J J Maaskant 1, P Ghiara 1, E J Kuipers 1, E Bloemena 1, T M Tadema 1, R R Townsend 1, K Tyagarajan 1, J M Crothers Jr 1, M A Monteiro 1, A Savio 1, J De Graaff 1
PMCID: PMC174033  PMID: 8675304

Abstract

Helicobacter pylori is involved in gastritis, gastric and duodenal ulcers, gastric adenocarcinoma, and mucosa-associated lymphoid tissue lymphoma. Earlier studies already suggested a role for autoimmune phenomena in H. pylori-linked disease. We now report that lipopolysaccharides (LPS) of H. pylori express Lewis y, Lewis x, and H type I blood group structures similar to those commonly occurring in gastric mucosa. Immunization of mice and rabbits with H. pylori cells or purified LPS induced an anti-Lewis x or y or anti-H type I response, yielding antibodies that bound human and murine gastric glandular tissue, granulocytes, adenocarcinoma, and mucosa-associated lymphoid tissue lymphoma cells. Experimental oral infections in mice or natural infection in humans yielded anti-Lewis antibodies also. The beta chain of gastric (H+,K+)-ATPase, the parietal cell proton pump involved in acid secretion, contained Lewis y epitopes; gastric mucin contained Lewis x and y antigenic determinants. Growth in mice of a hybridoma that secretes H. pylori-induced anti-Lewis y monoclonal antibodies resulted in histopathological evidence of gastritis, which indicates a direct pathogenic role for anti-Lewis antibodies. In conclusion, our observations demonstrate that molecular mimicry between H. pylori LPS and the host, based on Lewis antigens, and provide understanding of an autoimmune mechanism for H. pylori-associated type B gastritis.

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Selected References

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  1. Aspinall G. O., McDonald A. G., Pang H. Lipopolysaccharides of Campylobacter jejuni serotype O:19: structures of O antigen chains from the serostrain and two bacterial isolates from patients with the Guillain-Barré syndrome. Biochemistry. 1994 Jan 11;33(1):250–255. doi: 10.1021/bi00167a033. [DOI] [PubMed] [Google Scholar]
  2. Aspinall G. O., Monteiro M. A. Lipopolysaccharides of Helicobacter pylori strains P466 and MO19: structures of the O antigen and core oligosaccharide regions. Biochemistry. 1996 Feb 20;35(7):2498–2504. doi: 10.1021/bi951853k. [DOI] [PubMed] [Google Scholar]
  3. Aspinall G. O., Monteiro M. A., Pang H., Walsh E. J., Moran A. P. Lipopolysaccharide of the Helicobacter pylori type strain NCTC 11637 (ATCC 43504): structure of the O antigen chain and core oligosaccharide regions. Biochemistry. 1996 Feb 20;35(7):2489–2497. doi: 10.1021/bi951852s. [DOI] [PubMed] [Google Scholar]
  4. Burman P., Mårdh S., Norberg L., Karlsson F. A. Parietal cell antibodies in pernicious anemia inhibit H+, K+-adenosine triphosphatase, the proton pump of the stomach. Gastroenterology. 1989 Jun;96(6):1434–1438. doi: 10.1016/0016-5085(89)90509-x. [DOI] [PubMed] [Google Scholar]
  5. Callaghan J. M., Toh B. H., Pettitt J. M., Humphris D. C., Gleeson P. A. Poly-N-acetyllactosamine-specific tomato lectin interacts with gastric parietal cells. Identification of a tomato-lectin binding 60-90 X 10(3) Mr membrane glycoprotein of tubulovesicles. J Cell Sci. 1990 Apr;95(Pt 4):563–576. doi: 10.1242/jcs.95.4.563. [DOI] [PubMed] [Google Scholar]
  6. Chan N. W., Stangier K., Sherburne R., Taylor D. E., Zhang Y., Dovichi N. J., Palcic M. M. The biosynthesis of Lewis X in Helicobacter pylori. Glycobiology. 1995 Oct;5(7):683–688. doi: 10.1093/glycob/5.7.683. [DOI] [PubMed] [Google Scholar]
  7. Chow D. C., Forte J. G. Characterization of the beta-subunit of the H(+)-K(+)-ATPase using an inhibitory monoclonal antibody. Am J Physiol. 1993 Dec;265(6 Pt 1):C1562–C1570. doi: 10.1152/ajpcell.1993.265.6.C1562. [DOI] [PubMed] [Google Scholar]
  8. Crothers J. M., Jr, Chow D. C., Scalley M. L., Forte J. G. In vivo trafficking of nascent H(+)-K(+)-ATPase in rabbit parietal cells. Am J Physiol. 1995 Dec;269(6 Pt 1):G883–G891. doi: 10.1152/ajpgi.1995.269.6.G883. [DOI] [PubMed] [Google Scholar]
  9. Gleeson P. A. Glycoconjugates in autoimmunity. Biochim Biophys Acta. 1994 Dec 9;1197(3):237–255. doi: 10.1016/0304-4157(94)90009-4. [DOI] [PubMed] [Google Scholar]
  10. Goldkorn I., Gleeson P. A., Toh B. H. Gastric parietal cell antigens of 60-90, 92, and 100-120 kDa associated with autoimmune gastritis and pernicious anemia. Role of N-glycans in the structure and antigenicity of the 60-90-kDa component. J Biol Chem. 1989 Nov 5;264(31):18768–18774. [PubMed] [Google Scholar]
  11. Greiner A., Marx A., Heesemann J., Leebmann J., Schmausser B., Müller-Hermelink H. K. Idiotype identity in a MALT-type lymphoma and B cells in Helicobacter pylori associated chronic gastritis. Lab Invest. 1994 Apr;70(4):572–578. [PubMed] [Google Scholar]
  12. Gueant J. L., Kouvonen I., Michalski J. C., Masson C., Gräsbeck R., Nicolas J. P. Purification of human intrinsic factor using high-performance ion-exchange chromatography as the final step. FEBS Lett. 1985 May 6;184(1):14–19. doi: 10.1016/0014-5793(85)80643-8. [DOI] [PubMed] [Google Scholar]
  13. Isaacson P. G., Spencer J. Malignant lymphoma and autoimmune disease. Histopathology. 1993 May;22(5):509–510. doi: 10.1111/j.1365-2559.1993.tb00169.x. [DOI] [PubMed] [Google Scholar]
  14. Karlsson F. A., Burman P., Löf L., Mårdh S. Major parietal cell antigen in autoimmune gastritis with pernicious anemia is the acid-producing H+,K+-adenosine triphosphatase of the stomach. J Clin Invest. 1988 Feb;81(2):475–479. doi: 10.1172/JCI113344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kobayashi K., Sakamoto J., Kito T., Yamamura Y., Koshikawa T., Fujita M., Watanabe T., Nakazato H. Lewis blood group-related antigen expression in normal gastric epithelium, intestinal metaplasia, gastric adenoma, and gastric carcinoma. Am J Gastroenterol. 1993 Jun;88(6):919–924. [PubMed] [Google Scholar]
  16. Kuipers E. J., Thijs J. C., Festen H. P. The prevalence of Helicobacter pylori in peptic ulcer disease. Aliment Pharmacol Ther. 1995;9 (Suppl 2):59–69. [PubMed] [Google Scholar]
  17. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  18. Ma J. Y., Borch K., Mårdh S. Human gastric H,K-adenosine triphosphatase beta-subunit is a major autoantigen in atrophic corpus gastritis. Expression of the recombinant human glycoprotein in insect cells. Scand J Gastroenterol. 1994 Sep;29(9):790–794. doi: 10.3109/00365529409092512. [DOI] [PubMed] [Google Scholar]
  19. Ma J. Y., Borch K., Sjöstrand S. E., Janzon L., Mårdh S. Positive correlation between H,K-adenosine triphosphatase autoantibodies and Helicobacter pylori antibodies in patients with pernicious anemia. Scand J Gastroenterol. 1994 Nov;29(11):961–965. doi: 10.3109/00365529409094870. [DOI] [PubMed] [Google Scholar]
  20. Marchetti M., Aricò B., Burroni D., Figura N., Rappuoli R., Ghiara P. Development of a mouse model of Helicobacter pylori infection that mimics human disease. Science. 1995 Mar 17;267(5204):1655–1658. doi: 10.1126/science.7886456. [DOI] [PubMed] [Google Scholar]
  21. Mills S. D., Kurjanczyk L. A., Penner J. L. Antigenicity of Helicobacter pylori lipopolysaccharides. J Clin Microbiol. 1992 Dec;30(12):3175–3180. doi: 10.1128/jcm.30.12.3175-3180.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Moran A. P., Helander I. M., Kosunen T. U. Compositional analysis of Helicobacter pylori rough-form lipopolysaccharides. J Bacteriol. 1992 Feb;174(4):1370–1377. doi: 10.1128/jb.174.4.1370-1377.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Naparstek Y., Plotz P. H. The role of autoantibodies in autoimmune disease. Annu Rev Immunol. 1993;11:79–104. doi: 10.1146/annurev.iy.11.040193.000455. [DOI] [PubMed] [Google Scholar]
  24. Negrini R., Lisato L., Zanella I., Cavazzini L., Gullini S., Villanacci V., Poiesi C., Albertini A., Ghielmi S. Helicobacter pylori infection induces antibodies cross-reacting with human gastric mucosa. Gastroenterology. 1991 Aug;101(2):437–445. doi: 10.1016/0016-5085(91)90023-e. [DOI] [PubMed] [Google Scholar]
  25. Negrini R., Zanella I., Savio A., Poiesi C., Verardi R., Ghielmi S., Albertini A., Sangaletti O., Lazzaroni M., Bianchi Porro G. Serodiagnosis of Helicobacter pylori-associated gastritis with a monoclonal antibody competitive enzyme-linked immunosorbent assay. Scand J Gastroenterol. 1992 Jul;27(7):599–605. doi: 10.3109/00365529209000125. [DOI] [PubMed] [Google Scholar]
  26. Okamoto C. T., Karpilow J. M., Smolka A., Forte J. G. Isolation and characterization of gastric microsomal glycoproteins. Evidence for a glycosylated beta-subunit of the H+/K(+)-ATPase. Biochim Biophys Acta. 1990 Mar 1;1037(3):360–372. doi: 10.1016/0167-4838(90)90038-h. [DOI] [PubMed] [Google Scholar]
  27. Parsonnet J., Hansen S., Rodriguez L., Gelb A. B., Warnke R. A., Jellum E., Orentreich N., Vogelman J. H., Friedman G. D. Helicobacter pylori infection and gastric lymphoma. N Engl J Med. 1994 May 5;330(18):1267–1271. doi: 10.1056/NEJM199405053301803. [DOI] [PubMed] [Google Scholar]
  28. Sarnesto A., Köhlin T., Hindsgaul O., Thurin J., Blaszczyk-Thurin M. Purification of the secretor-type beta-galactoside alpha 1----2-fucosyltransferase from human serum. J Biol Chem. 1992 Feb 5;267(4):2737–2744. [PubMed] [Google Scholar]
  29. Sherburne R., Taylor D. E. Helicobacter pylori expresses a complex surface carbohydrate, Lewis X. Infect Immun. 1995 Dec;63(12):4564–4568. doi: 10.1128/iai.63.12.4564-4568.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Stöckl J., Majdic O., Rosenkranz A., Fiebiger E., Kniep B., Stockinger H., Knapp W. Monoclonal antibodies to the carbohydrate structure Lewis(x) stimulate the adhesive activity of leukocyte integrin CD11b/CD18 (CR3, Mac-1, alpha m beta 2) on human granulocytes. J Leukoc Biol. 1993 May;53(5):541–549. doi: 10.1002/jlb.53.5.541. [DOI] [PubMed] [Google Scholar]
  31. Toh B. H., Gleeson P. A., Simpson R. J., Moritz R. L., Callaghan J. M., Goldkorn I., Jones C. M., Martinelli T. M., Mu F. T., Humphris D. C. The 60- to 90-kDa parietal cell autoantigen associated with autoimmune gastritis is a beta subunit of the gastric H+/K(+)-ATPase (proton pump). Proc Natl Acad Sci U S A. 1990 Aug;87(16):6418–6422. doi: 10.1073/pnas.87.16.6418. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Tsai C. M., Frasch C. E. A sensitive silver stain for detecting lipopolysaccharides in polyacrylamide gels. Anal Biochem. 1982 Jan 1;119(1):115–119. doi: 10.1016/0003-2697(82)90673-x. [DOI] [PubMed] [Google Scholar]
  33. Van Dam G. J., Bergwerff A. A., Thomas-Oates J. E., Rotmans J. P., Kamerling J. P., Vliegenthart J. F., Deelder A. M. The immunologically reactive O-linked polysaccharide chains derived from circulating cathodic antigen isolated from the human blood fluke Schistosoma mansoni have Lewis x as repeating unit. Eur J Biochem. 1994 Oct 1;225(1):467–482. doi: 10.1111/j.1432-1033.1994.00467.x. [DOI] [PubMed] [Google Scholar]
  34. Velupillai P., Harn D. A. Oligosaccharide-specific induction of interleukin 10 production by B220+ cells from schistosome-infected mice: a mechanism for regulation of CD4+ T-cell subsets. Proc Natl Acad Sci U S A. 1994 Jan 4;91(1):18–22. doi: 10.1073/pnas.91.1.18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Vollmers H. P., Dämmrich J., Ribbert H., Grassel S., Debus S., Heesemannn J., Müller-Hermelink H. K. Human monoclonal antibodies from stomach carcinoma patients react with Helicobacter pylori and stimulate stomach cancer cells in vitro. Cancer. 1994 Sep 1;74(5):1525–1532. doi: 10.1002/1097-0142(19940901)74:5<1525::aid-cncr2820740506>3.0.co;2-t. [DOI] [PubMed] [Google Scholar]
  36. Weitzhandler M., Kadlecek D., Avdalovic N., Forte J. G., Chow D., Townsend R. R. Monosaccharide and oligosaccharide analysis of proteins transferred to polyvinylidene fluoride membranes after sodium dodecyl sulfate-polyacrylamide gel electrophoresis. J Biol Chem. 1993 Mar 5;268(7):5121–5130. [PubMed] [Google Scholar]
  37. de Vries T., Srnka C. A., Palcic M. M., Swiedler S. J., van den Eijnden D. H., Macher B. A. Acceptor specificity of different length constructs of human recombinant alpha 1,3/4-fucosyltransferases. Replacement of the stem region and the transmembrane domain of fucosyltransferase V by protein A results in an enzyme with GDP-fucose hydrolyzing activity. J Biol Chem. 1995 Apr 14;270(15):8712–8722. doi: 10.1074/jbc.270.15.8712. [DOI] [PubMed] [Google Scholar]

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