Helicobacter pylori infection: regulatory role of cytokines in inflammation and allergy



Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

Helicobacter pylori is a Gram-negative bacterium that chronically infects the stomach of more than 50% of human population and represents the major cause of gastroduodenal pathologies. The H. pylori infection is followed by local inflammatory response in gastric mucosa and proinflammatory cytokine production, and preferably elicits a T-helper 1 (Thl) immune response. Bronchial asthma and allergic diseases are orchestrated by Th2 cytokines. A negative association between the H. pylori infection and frequency of allergic diseases was found. Investigations of possible molecular mechanisms of the association are required for research of novel strategies of prevention and treatment of allergic diseases.

About the authors

E A Varyushina

State Scientific Center State Research Institute of Highly Pure Biopreparations

Email: elenavaryush@gmail.com
State Scientific Center State Research Institute of Highly Pure Biopreparations

A S Simbirtsev

State Scientific Center State Research Institute of Highly Pure Biopreparations

State Scientific Center State Research Institute of Highly Pure Biopreparations

References

  1. ВарюшинаЕ.А., КозловаИ.П., Котов А.Ю., Симбирцев А.С. Продукция провоспалительных цитокинов в слизистой оболочке желудка у детей с хроническими гастродуоденальными заболеваниями при инфекции Helicobacter pylori. Рос. иммунол. журн. 2009, т. 3, № 1, с. 72-83.
  2. Козлова И.П. Иммунологические особенности детей с Helicobacter pylori-ассоциированной гастродуоденальной патологией. Автореферат... канд. мед. наук. СПб, 2002, 22 с.
  3. Blaser M.J., Atherton J.C. Helicobacter pylori persistence: biology and disease J. Clin. Invest. 2004, v. 113, p. 321-333.
  4. Parsonnet J., Friedman G., Vandersteen D. et al. Helicobacter pylori infection and gastric lymphoma. N. Engl. J. Med. 1994, v. 330, p. 1267-1271.
  5. Smith M., Hold G., Eahara E., El-Omar E. Cellular and molecular aspects of gastric cancer. World J. Gastroenterol. 2006, v. 12, p. 2979-2990.
  6. CremoniniE, Gasbarrini A. Atopy, Helicobacter pylori and hygiene hypothesis. European Journal of Gastroenterology and Hepatology. 2003, v. 15, p. 635-636.
  7. Wjst M. Does Helicobacter pylori protect against asthma and allergy. Gut. 2008, v. 57, p. 1178-1179.
  8. Chen Y, Blaser M.J. Inverse associations of Helicobacter pylori protection with asthma and allergy. Arch. Intern. Med. 2007, v. 167, p. 821-827.
  9. Dunn B.E., Cohen H., Blaser M.J. Helicobacter pylori. Clin. Microbiol. Reviews. 1997, v. 10, p. 720-741.
  10. Beswick E., Suarez G., Reyes V. H. pylori and host interactions that influence pathogenesis .World J. Gastroenterol. 2006, v. 12, p. 5599-5605.
  11. Loughlin M.F., Barnard F.M., Jenkins D.et al. Helicobacter pylori mutants defective in RuvC Holliday junction resolvase display reduced macrophage survival and spontaneous clearance from the murine gastric mucosa. Infect. Immune. 2003, v. 71, p. 2022-2031.
  12. Rieder G., Fischer W, Rainer H. Interaction of Helicobacter pylori with host cells: function of secreted and translocated molecules. Current Opinion in Microbiology. 2005, v. 8, p. 67-73.
  13. Bartchewsky W Jr., Martini M.R., Masiero M. et al. Effect of Helicobacter pylori infection on IL-8, IL-1 beta and COX-2 production in patients with chronic gastritis and gastric cancer. Scand. J. Gastroenterol. 2009, v. 44, p. 154-161.
  14. Kuipers E.J., Perez-Perez G.I., Meuwissen S.G. et al. Helicobacter pylori and atrophic gastritis: importance of the cagA status. J. Natl. Cancer Inst. 1995, v. 87, p. 1777-1780.
  15. Rieder G., FischerW, Rainer H. Interaction of Helicobacter pylori with host cells: function of secreted and translocated molecules. Current Opinion in Microbiology. 2005, v. 8, p. 67-73.
  16. Amedei A., Cappon A., Codolo G. et al. The neutrophil-activating protein of Helicobacter pylori promote Th1 immune response. J. Clin. Invest. 2006, v. 116, p. 1092-1101.
  17. Wang C.A., Liu Y.C., Du S.Y. et al. Helicobacter pylori neutrophil-activating protein promotes myeloperoxidase release from human Neutrophils. Biochem. Biophys. Res. Commun. 2008, v. 377, p. 52-56.
  18. Codolo G., Mazzi P., Amedei A. et al. The neutrophil-activating protein of Helicobacter pylori down-modulates Th2 inflammation in ovalbumin-induced allergic astma. Cell. Microbiol. 2008, v. 10, p. 2355-2363.
  19. Portal-Celhay C, Perez-Perez G.I. Immune responses to Helicobacter pylori colonization: mechanisms and clinical outcomes. Clinical Science. 2006, v. 110, p. 305-314.
  20. Scott Algood H.M., Cover T.L. Helicobacter pylori persistence: an overview of interactions between H. pylori and host immune defenses. Clin. Microbiol. Reviews. 2006, v. 19, p. 597-613.
  21. Jonsson K., Guo B.P, Monstein H.J. et al. Molecular cloning and characterization of two Helicobacter pylori genes coding for plasminogen-binding proteins. Proc. Natl. Acad. Sci. USA. 2004, v. 101, p. 1852-1857.
  22. BamfordK., FanX., Crowe S. et al. Lymphocytes in the human gastric mucosa during Helicobacter pylori have a T helper cell 1 phenotype. Gastroenterology. 1998, v.114, p. 482-492.
  23. Sawai N., Kita M., Kodama T. et al. Role of g interferon in Helicobacter pylori induced gastric inflammatory responses in a mouse model. Infect. Immun. 1999, v. 67, p. 279-285.
  24. Demi L., Aigner M., Decker J. et al. Characterization of the Helicobacter pylori cysteine-rich protein A as a T-helper cell type 1 polarizing agent. Infect. Immun. 2005, v. 73, p. 4732- 4742.
  25. Raghavan S., Holmgren J. CD4+ CD25+ suppressor T cell regulate pathogen induced inflammation and disease. FEMS Immunol. Medical Microbiol. 2005, v. 44, p. 121-127.
  26. Graham D., Opekun A., Osato M. et al. Challenge model for Helicobacter pylori infection in human volunteers. Gut. 2004, v. 53, p. 1235-1243.
  27. D'Elios M.M., Amadei A., Benagiano M. et al. Helicobacter pylori, T cells and cytokines: the «dangerous liaisons». FEMS Immunol. Med. Microbiol. 2005, v. 1. p. 113-119.
  28. Lindholm C, Quiding-Jarbrink M., Lonroth H. et al. Local cytokine response in Helicobacter pylori-infected subjects. Infect. Immun. 1998, v. 66, p. 5964-5971.
  29. Luzza F, Parrello T, Monteleone G. et al. Up-regulation of IL-17 is assiciated withbioactive IL-8 expression in Helicobacter pylori-infected human gastric mucosa. J. Immunol. 2000, v. 165, p. 5332-5337.
  30. Caruso R., Fina D., Paoluzi OA. et al. IL-23-mediated regulation of IL-17 production in Helicobacter pylori-infected gastric mucosa. Eur. J. Immunol. 2008, v. 38, p. 470-478.
  31. El-Omar E. The importance of interleukin-lb in Helicobacter pylori associated disease. Gut. 2001, v. 48, p. 743-747.
  32. Bhattacharyya A., Pathak S., Datta S. et al. Mitogen-activated protein kinases and nuclear factor-kB regulate Helicobacter pylori-mediated interleukin-8 release from macrophages. Biochem. J. 2002, v. 8, p. 121-129.
  33. Innocenti M., Svennerholm A.-M., Quiding-Jarbrink M. Helicobacter pylori lipopolisaccharides preferentially induce CXC chemokine production in human monocytes. Infection and Immunity. 2001, v. 69, p. 3800-3808.
  34. Basso D., Scringer M., Toma A., Navaglia F et al. Helicobacter pylori infection enhances mucosal interleukin-1 beta, interleu-kin-6, and the soluble receptor of interleukin-2. Int. J. Clin. Lab. Res. 1996, v. 26, p. 207-210.
  35. Bodger K., Wyatt J.I., Heatley R.V. Gastric mucosal secretion of interleukin-10: relations to histopathology Helicobacter pylori status, and tumor necrosis factor-alpha secretion. Gut. 1997, v. 40, p. 739-744.
  36. Crabtree J., Wyatt J., Trejdosiewicz L. et al. Interleukin-8 expression in Helicobacter pylori infected, normal, and neoplastic gas-troduodenal mucosa. J. Clin. Path. 1994, v. 47, p. 61-66.
  37. Katagiri M., Asaka M., Kobayashi M. et al. Increased cytokine production by gastric mucosa in patients with Helicobacter pylori infection. J. Clin. Gastroenterol. 1997, v. 25, Suppl. 1, p. 211-214.
  38. Yamaoka Y, Kita M., Sawai N. et al. Induction of various cytokines and development of severe mucosal inflammation by cagA gene positive Helicobacter pylori strains. Gut. 1997, v. 41, p. 442-451. 17.
  39. Rad R., Dossumbekova A., Neu B. et al. Cytokine gene polymorphisms influence mucosal cytokine expression, gastric inflammation, and host specific colonisation during Helicobacter pylori infection. Gut. 2004, v. 53, p. 1082-1089.
  40. Bayraktaroglu Т., Sukru Aras A., Aydemyr S. et al. Serum levels of tumor necrosis factor-a, interleukin-6 and interleukin-8 are not increased in dyspeptic patients with Helicobacter pylori-associated gastritis. Mediators of Inflammation. 2004, v. 13, p. 25-28.
  41. Rad R., Prinz C, Neu B. et al. Synergistic effect of Helicobacter pylori virulence factors and interleukin-1 polymorphisms for the development of severe histological in the gastric mucosa. J. Infect. Dis. 2003, v. 188, p. 271-281.
  42. Xuan J., Deguchi R., Watanabe S. et al. Relationship between IL-lbeta gene polymorphism and gastric mucosal IL-lbeta levels in patients with Helicobacter pylori infection. J. Gastroenterol. 2005, v. 40, p. 796-801.
  43. Takashima M., FuritaT., Hanai H. et al. Effects of Helicobacter pylori infection on gastric acid secretion and serum gastrin levels in Mongolian gerbils. Gut. 2001, v. 48, p. 765-773.
  44. Togawa S., Joh T., Itoh M. et al. Interleukin-2 gene polymorphisms associated with increased risk of gastric athrophy from Helicobacter pylori infection. Helicobacter. 2005, v. 10, p. 172-178.
  45. Pessi Т., Virta M., Adjers K. et al. Genetic and environmental factors in the immunopathogenesis of atopy: interaction of Helicobacter pylori infection and IL-4 genetics. Int. Arch. Allergy Immunol. 2005, v. 137, p. 282-288.
  46. Oderda G., Vivenza D., Rapa A. et al. Increased interleukin-10 in Helicobacter pylori infection could be involved in the mechanism protecting from allergy. J. Pediatr. Gastroenterol. Nutr. 2007, v. 45, p. 301-305.
  47. Atherton J.C., Blaser M. Coadaptation of Helicobacter pylori and humans: ancient history, modern implication. J. Clin. Invest. 2009, v. 119, p. 2475-2487.
  48. Robinson K. et al. Helicobacter pylori-induced peptic ulcer disease is associated with inadequate regulatory T cell responses. Gut. 2008, v. 57, p. 1375-1385.
  49. D'Elios M.M., Codolo G., Amedei A. et al. Helicobacter pylori, asthma and allergy. FEMS Immunol. Med. Microbiol. 2009, v. 56, p. 1-8.
  50. Yamamura F, Yoshikawa N., Akita Y. et al. Relationship between Helicobacter pylori infection and histological features of gastritis in biopsy specimens in gastroduodenal diseases, including eve-luation of diagnosis by polymerase chain reaction assay. J. Gastroenterol. 1999, v. 34, p. 461-466.
  51. Alvarez-Arellano L., Camorlinga-Ponce M., Maldonado-Bernal C., Torres J. Activation of human neutrophils with Helicobacter pylori and the role of Toll-like receptors 2 and 4 in the response. FEMS Immunol. Med. Microbiol. 2007, v. 51, p. 473-479.
  52. Crabtree J.E., Kersulyte D., Hernandez V. et al. Helicobacter pylori induction of IL-8 synthesis in gastric epithelial cells depends on genes throughout the cag pathogenisity island [abstract]. Gut. 1997, v. 40 (suppl. 1), p. 69.
  53. Schmausser В., Josenhans C, Endrich S. et al. Down regulation of CXCR1 and CXCR2 expression on human neutrophils by Helicobacter pylori: a new pathomechanism in H. pylori infection? Infection and Immunity. 2004, v. 72, p. 6773-6779.
  54. Berstad A., Brandtzaeg P, Stave R. etal. Epithelium related deposition of activated complement in Helicobacter pylori associated gastritis. Gut. 1997, v. 40, p. 196-203.
  55. Whitney A.E., Guarner J., HutwagnerL., GoldB.D. Helicobacter pylori gastritis in children and adults: comparative histopathologic study. Ann. Diagn. Pathol. 2000, v. 5, p. 279-285.
  56. Dzierzanowska-Fangrat K., Raeiszadeh M., Dzierzanowska D. et al. IgG subclass response to Helicobacter pylori and Cag A antigens in children. Clin. Exp. Immunol. 2003, v. 134, p. 442-446.
  57. Maciorkowska E., Panasiuk A., Kaczmarski M. Concentrations of gastric mucosal cytokines in children with food allergy and Helicobacter pylori infection. World J. Gastroenterol. 2005, v. 11, p. 6751-6756.
  58. Dzierzanowska-Fangrat K., Michalkiewicz J., Cielecka-Kuszyk J. etal. Enhanced gastric IL-18 mRNA expression in Helicobacter pylori-infected children is associated with macrophage infiltration, IL-8, and IL-1 beta mRNA expression. Eur. J. Gastroene-trol. Hepatol. 2008, v. 20, p. 314-319.
  59. Harris P.R. et al. Helicobacter pylori gastritis in children is associated with a regulatory T-cell response. Gastroenterology. 2008, v. 134, p. 491-499.
  60. Shimizu T, Haruna H., Ohtsuka Y et al. Cytokines in the gastric mucosa of children with Helicobacter pylori infection. Acta Paediatr. 2004, v. 93, p. 322-326.
  61. Bontems P., Robert F, Van Gossum A., Cadranel S., Mascart F Helicobacter pylori modulation of gastric and duodenal mucosal T cell cytokines secretions in children compared with adults. Helicobacter. 2003, v. 8, p. 216-226.
  62. Lopes A.I., Quiding-Jarbrink M., Palha A. et al. Cytokine expression in pediatric Helicobacter pylori infection. Clinical and Diagnostic Laboratory Immunology. 2005, v. 12, p. 994-1002.
  63. Queiroz D., Bittencourt P., Guerra J. et al. IL-11RN polymorphism and cagA-positive Helicobacter pylori strains increase the risk of duodenal ulcer in children. Pediatr. Res. 2005, v. 58, p. 892-896.

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright © Pharmarus Print Media, 2009



This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies