Возможное участие бактерий рода Helicobacter в патогенезе гепатобилиарных заболеваний
Аннотация
Цель обзора. Представить анализ данных литературы о возможном участии бактерий рода Helicobacter в патогенезе заболеваний гепатобилиарной системы.
Последние данные литературы. В ходе научных исследований, проведенных в последнее время, бактерии выявлены в желчи, тканях печени, слизистой оболочке желчного пузыря и желчных протоков, что свидетельствует о их способности колонизировать органы гепатобилиарной системы. На существование возможной связи бактерий рода Helicobacter с развитием хронического холецистита, желчнокаменной болезни, холангио- и гепатокарциномы указывают многочисленные исследования с использованием молекулярных, гистологических, микроскопических, бактериологических, иммунологических методов, опыты на биологических моделях. Расшифровка патогенетических механизмов с участием этих микроорганизмов открывает перспективу применения антигеликобактерной терапии для лечения и профилактики заболеваний гепатобилиарной системы.
Заключение. Накопленные сведения о роли H. pylori и других видов рода Helicobacter в развитии патологии печени, желчного пузыря и желчевыводящих путей позволяют сделать первоначальные выводы о их возможном участии в этих процессах. Несмотря на противоречивость мнений, это новое быстро развивающееся направление можно отнести к весьма перспективному и требующему продолжения исследований в данной области.
Список литературы
1. Момыналиев К.Т., Смирнова О.В., Челищева В.В. и др. Идентификация H. pylori в желчных камнях у детей // Рос. журн. гастроэнтерол. гепатол. колопроктол. – 2003. – Т. 13, № 3 (прил. 19). – С. 17–20.
2. Яковенко А.В., Григорьев П.Я., Обуховский Б.И. и др. Helicobacter pylori-инфекция у больных циррозом печени: диагностика и вопросы терапии // Эксп. клин. гастроэнтерол. – 2006. – № 1. – С. 84–88.
3. Ananieva O., Nilsson I., Vorobjova T. et al. Immune responses to bile-tolerant Helicobacter species in patients with chronic liver diseases a randomized population group, and healthy blood donors // Clin. Diag. Lab. Immun. – 2002. – Vol. 9. – P. 1160–1164.
4. Apostolov E., AbuAl-Soud W., Nilsson I. et al. Helicobacter pylori and other Helicobacter species in gallbladder and liver of patients with chronic cholecystitis detected by immunological and molecular methods // Scand. J. Gastroenterol. – 2005. – Vol. 40. – P. 96–102.
5. Avenaud P., Marais A., Monteiro L. et al. Detection of Helicobacter species in the liver of patients with and without primary liver carcinoma // Cancer. – 2000. – Vol. 89. – P. 1431–1439.
6. Belzer C., Stoof J., Beckwith C.S. et al. Differential regulation of urease activity in Helicobacter hepaticus and Helicobacter pylori // Microbiology. – 2006. – Vol. 151, N 12. – P. 3989–3995.
7. Bohr U.R.M., Annibale B., Franceschi F. et al. Extragastric manifestations of Helicobacter pylori and other Helicobacters // Helicobacter. – 2007. – Vol. 12, N 1. – P. 45–53.
8. Bulajic M., Maisonneuve P., Schneider-Brachert W. et al. Helicobacter pylori and the risk of benign and malignant biliary tract disease // Cancer. – 2002. – Vol. 95. – P. 1946–1953.
9. Caldwell M.T.P., McDermott M., Jazrawi S. et al. Helicobacter pylori infection increases following cholecystectomy // Ir. J. Med. Sci. – 1995. – Vol. 164. – P. 52–55.
10. Camorlinga-Ponce M., Romo C., Gonzalez-Valencia G. et al. Topographical localisation of cagA positive and cagA negative Helicobacter pylori strains in the gastric mucosa; an in situ hybridisation study // J. Clin. Pathol. – 2004. – Vol. 57. – P. 822–828.
11. Caygill C.P.J. Hill M.J., Braddick M. et al. Cancer mortality in chronic typhoid and paratyphoid carriers // Lancet. – 1994. – Vol. 343. – P. 83.
12. Chen D.F., Hu L., Yi P., Fang D.C. et al. H. pylori exist in the gallbladder mucosa of patients with chronic cholecystitis // World J. Gastroenterol. – 2007. – Vol. 13, N 10. – P. 1608–1611.
13. Chen D.F., Hu L., Yi P., Liu W.W. et al. H. pylori are associated with chronic cholecystitis // World J. Gastroenterol. – 2007. – Vol. 13, N 7. – P. 1119–1122.
14. Chen W., Li D., Cannan R.J., Stubbs R.S. Common presence of Helicobacter DNA in the gallbladder of patients with gallstone diseases and controls // Dig. Liver Dis. – 2003. – Vol. 35. – P. 237–243.
15. De Magalhaes Queiroz D.M., Santos A. Isolation of a Helicobacter strain from the human liver // Gastroenterology. – 2001. – Vol. 121. – P. 1023–1024.
16. Dore M.P., Graham D.Y. Pathogenesis of duodenal ulcer disease: the rest of story // Baillieres Best Pract. Res. Clin. Gastroenterol. – 2000. – Vol. 14, N 1. – P. 97–107.
17. Dore M.P., Realdi G., Mura D. et al. Helicobacter infection in patients with HCV-related chronic hepatitis, cirrhosis, and hepatocellular carcinoma // Dig. Dis. Sci.– 2002. – Vol. 47. – P. 1638–1643.
18. El-Serag H.B. Hepatocellular carcinoma and hepatitis C in the United States // Hepatology. – 2002. – Vol. 36 – P. 74–83.
19. Fan X.G., Peng X.N., Huang Y. et al. Helicobacter species ribosomal DNA recovered from the liver tissue of Chinese patients with primary hepatocellular carcinoma // Clin. Infect. Dis. – 2002. – Vol. 35. – P. 1555–1557.
20. Figura N., Cetta F., Angelico M. et al. Most Helicobacter pylori – infected patients have specific antibodies, and some also have H. pylori antigens and genomic material in bile: Is it a risk factor for gallstone formation? // Dig. Dis. Sci. – 1998. – Vol. 48. – P. 854.
21. Fox J.G., Dewhirst F.E., Shen Z. et al. Hepatic Helicobacter species identified in bile and gallbladder tissue from Chileans with chronic cholecystitis // Gastroenterology. – 1998. – Vol. 114. – P. 755–763.
22. Fox J.G., Dewhirst F.E., Tully J.G. et al. Helicobacter hepaticus sp. nov., a microaerophilic bacterium isolated from livers and intestinal mucosal scrapings from mice // J. Clin. Microbiol. – 1994. – Vol. 32. – P. 1238–1245.
23. Fox J.G., Lee A. The role of Helicobacter species in gastrointestinal tract diseases of animals // Lab. Anim. Sci. – 1997. – Vol. 47. – P. 222–255.
24. Fox J.G., Li X., Yan L. et al. Chronic proliferative hepatitis in A/JCr mice associated with persistent Helicobacter hepaticus infection: a model of Helicobacter-induced carcinogenesis // Infect. Immun. – 1996. – Vol. 64. – P. 1548–1558.
25. Fox J.G., Li X., Yan L. et al. Persistent hepatitis and enterocolitis in germfree mice infected with Helicobacter hepaticus // Infect. Immun. – 1996. – Vol. 64. – P. 3673–3681.
26. Fox J.G., Taylor N.S., Nowe S. et al. Helicobacter anseris sp. nov. and Helicobacter brantae sp. nov., isolated from feces of resident Canada geese in the greater Boston area // Appl. Environ. Microbiol. – 2006. – Vol. 72. – P. 4633–4637.
27. Fukuda K., Kuroki T., Tajima Y. et al. Comparative analysis of Helicobacter DNAs and biliary pathology in patients with and without hepatobiliary cancer // Carcinogenesis. – 2002. – Vol. 23. – P. 1927–1931.
28. Garrity G.M., Bell J.A., Liburn T., Family I.I. Helicobacteriaceae fam. nov. // Brennen D.J., Krieg N.R., Staley J.T. / Bergey’s manual of determinative bacteriology. – N.-Y.: Springer, 2005. – P. 1168–1194.
29. Graham D.Y., Osato M.S. H. pylori in the pathogenesis of duodenal ulcer: interaction between duodenal acid load, bile, and H. pylori // Am. J. Gastroenterol. – 2000. – Vol. 95, N 1. – P. 87–91.
30. Hanninen M.L. Sensitivity of Helicobacter pylori to different bile salts // Eur. J. Clin. Microbiol. Infect. Dis. – 1991. – Vol. 10. – P. 515–518.
31. Harada K., Ozak S., Kono N. et al. Frequent molecular identification of Campylobacter but not Helicobacter genus in bile and biliary epithelium in hepatolithiasis // J. Pathol. – 2001. – Vol. 193. – P. 218–223.
32. Hynes S.O., Teneberg S., Roche N. et al. Glycoconjugate binding of gastric and enterohepatic Helicobacter spp. // Infect. Immun. – 2003. – Vol. 71. – P. 2976–2980.
33. IARC Working Group on the Evaluation of Carcinogenesis Risks to Humans. Monographs. Lyon. – 1994. – Vol. 61. – P. 1–241.
34. Ito K., Nakamura M., Toda G. et al. Potential role of Helicobacter pylori in hepatocancerogenesis // Int. J. Mol. Med. – 2004. – Vol. 13. – P. 221–227.
35. Johnson W.M., Lior H. A new heat-labile cytolethal distending toxin (CLDT) produced by Campylobacter spp. // Microb. Pathog. – 1988. – Vol. 4. – P. 115–126.
36. Johnson W.M., Lior H. A new heat-labile cytolethal distending toxin (CLDT) produced by Escherichia coli isolates from clinical material // Microb. Pathog. – 1988. – Vol. 4. – P. 103–113.
37. Kawai M., Iwahashi M., Uchiyama K. et al. Gram positive cocci are associated with the formation of completely pure cholesterol stones // Am. J. Gastroenterol. – 2002. – Vol. 97. – P. 83–88.
38. Kelly S.M., Pitcher M.C.L., Farmery S.M. et al. Isolation of Helicobacter pylori from feces with dyspepsia in the United Kingdom // Gastroenterology. – 1994. – Vol. 107. – P. 1671–1674.
39. Kontrek S.J., Gonciarz M., Gonciarz Z. et al. Progastrin and its products from patients with chronic viral hepatitis and liver cirrhosis // Scand. J. Gastroenterol. – 2003. – Vol. 38. – P. 643–647.
40. Kuntz E., Kuntz H.D. Hepatology. Principles and practice. – Heidelberg: Springer Medizin Verlag, 2006.
41. Kuroki T., Fukuda K., Yamanouchi K. et al. Helicobacter pylori accelerates the biliary epithelial cell proliferation activity in hepatolithiasis // Hepatogastroenterology. – 2002. – Vol. 49. – P. 648–651.
42. Lee D.K., Tarr P.I., Haigh W.C. et al. Bacterial DNA in mixed cholesterol gallstones // Am. J. Gastroenterol. – 1999. – Vol. 94, N 12. – P. 3502–3506.
43. Leung J.W., Liu Y.L., Leung P.S. et al. Expression of bacterial beta-glucuronidase in human bile: an in vitro study // Gastrointest. Endosc. – 2001. – Vol. 54, N 3. – P. 346–350.
44. Mammen M.P.J., Aronson N.E., Edenfield W.J. et al. Recurrent Helicobacter cinaedi bacteremia in a patient infected with human immunodeficiency virus: case report // Clin. Infect. Dis. – 1995. – Vol. 21. – P. 1055.
45. Maurer K.J., Ihrig M.M., Rogers A.B. et al. Identification of cholelithogenic enterohepatic Helicobacter species and their role in murine cholesterol gallstone formation // Gastroenterology. – 2000. – Vol. 93, N 7. – P. 1023–1033.
46. Monstein H.J., Jonsson Y., Zdolsek J. et al. Identification of Helicobacter pylori DNA in human cholesterol gallstones // Scand. J. Gastroenterol. – 2002. – Vol. 37, N 1. – P. 112–119.
47. Moyaert H., Decostere A., Vandamme P. et al. Helicobacter equorum sp. nov., a urease-negative Helicobacter species isolated from horse feces // Int. J. Syst. Evol. Microbiol. – 2007. – Vol. 57. – P. 213–218.
48. Nieuwkerk C.M.J., Kuipers E.J. Liver cirrhosis and pepric ulcer disease: a correlation with Helicobacter pylori? // Neth. J. Med. – 2000. – Vol. 56. – P. 203–205.
49. Nilsson H.O., Mulchandani R., Stenram U. et al. Helicobacter species identified in liver from patients with cholangiocarcinoma and hepatocellular carcinoma // Gastroenterology. – 2001. – Vol. 120. – P. 323–324.
50. Offner G.D., Gong D., Afdhal N.H. Identification of a 130 kilodalton human biliary concanvalin A binding protein as aminopeptidase N // Gastroenterol. – 1994. – Vol. 106. – P. 755–762.
51. Okuda J., Kurazono H., Takeda Y. Distribution of the cytolethal distending toxin A gene (cdtA) among species of Shigella and Vibrio, and cloning and sequencing of the cdt gene from Shigella dysenteriae // Microb. Pathog. – 1995. – Vol. 18. – P. 167–172.
52. Orlicek S.L., Welch D.F., Kuhls T.L. Helicobacter fennelliae bacteremia in a child with leukemia // Infect. Dis. Clin. Pract. – 1994. – Vol. 3. – P. 450–451.
53. Pellicano R., Leone N., Berrutti M. et al.. Helicobacter pylori seroprevalence in hepatitis C virus positive patients with cirrhosis // J. Hepatol. – 2000. – Vol. 33. – P. 648–650.
54. Pickett C.L., Pesci E.C., Cottle D.L. et al. Prevalence of cytolethal distending toxin production in Campylobacter jejuni and relatedness of Campylobacter sp. cdtB gene // Infect. Immun. – 1996. – Vol. 64. – P. 2070–2078.
55. Ponzetto A., Pellicano R., Leone N. et al. Helicobacter pylori seroprevalence in cirrhotic patients with hepatitis B virus infection // Neth. J. Med. – 2000. – Vol. 56. – P. 206–210.
56. Ponzetto A., Pellicano R., Pedaelli A. et al. Helicobacter pylori infection in patients with hepatitis C virus positive chronic liver diseases // New Microbiol. – 2003. – Vol. 26. – P. 321–328.
57. Rocha M., Avenaud P., Menard A. et al. Association of Helicobacter species with hepatitis C cirrhosis with or without hepatocellular carcinoma // Gut. – 2005. – Vol. 54. – P. 396–401.
58. Silva C.P., Pereira J.C., Goncalves Oliveira A. et al. Association of the presence of Helicobacter pylori in gallbladder tissue with cholelithiasis and cholecystitis // J. Clin. Microbiol. – 2003. – Vol. 41. – P. 5615–5618.
59. Sorlin P., Vandamme P., Nortier J. et al. Recurrent Flexispira rappini bacteremia in an adult patient undergoing hemodialysis: case report // J. Clin. Microbiol. – 1999. – Vol. 37. – P. 1319–1323.
60. Srivatanakul P. Epidemiology of liver cancer in Thailand // Asian Pac. J. Cancer Prev. – 2001. – Vol. 2. – P. 117–121.
61. Stalke P., Abu Al-Soud W., Bielawski K.P. et al. Detection of Helicobacter species in liver and stomach tissues of patients with chronic liver disease using polymerase chain reaction – denaturing gradient gel electrophoresis and immunohistochemistry // Scand. J. Gastroenterol. – 2005. – Vol. 40. – P. 1032–1041.
62. Suganuma M., Kurusu M., Okabe S. et al. Helicobacter pylori membrane protein 1: a new carcinogenic factor of Helicobacter pylori // Cancer Res. – 2001. – Vol. 61. – P. 6356–6359.
63. Swidsinski A., Lee S.P. The role of bacteria in gallstone pathogenesis // Front. Biosci. – 2001. – Vol. 1, N 6. – P. 93–103.
64. Taylor N.S., Fox J.G., Yan L. In vitro hepatotoxic factor in Helicobacter hepaticus, Helicobacter pylori and other Helicobacter species // J. Med. Microbiol. – 1995. – Vol. 42. – P. 48–52.
65. Thomas J.E., Gibson G.R., Darboe M.K. et al. Isolation of Helicobacter pylori from human feces // Lancet. – 1995. – Vol. 340. – P. 1194–1195.
66. Van den Bulck K., Decostere A., Baele M. et al. Helicobacter cynogastricus sp. nov., isolated from the canine gastric mucosa // Int. J. Syst. Evol. Microbiol. – 2006. – Vol. 56. – P. 1559–1564.
67. Vitetta L., Best S.P., Sali A. Single and multiple cholesterol gallstones and the influence of bacteria // Med. Hypotheses. – 2000. – Vol. 55, N 6. – P. 502–506.
68. Vorobjova T., Nilsson I., Terjajev S. et al. Serum antibodies to enterohepatic Helicobacter spp. in patients with liver diseases and a population with high prevalence of H. pylori infection // Dig. Liver Dis. – 2006. – Vol. 38. – P. 171–176.
69. Ward J.M., Anver M.R., Haines D.C. et al. Chronic active hepatitis in mice caused by Helicobacter hepaticus // Am. J. Pathol. – 1994. – Vol. 145. – P. 959–968.
70. Ward J.M., Fox J.G., Anver M.R. et al. Chronic active hepatitis and associated liver tumors in mice caused by a persistent bacterial infection with a novel Helicobacters species // J. Natl. Cancer Inst. – 1994. – Vol. 86. – P. 1222–1227.
71. Welton J.C., Marr J.S., Friedman S.M. Association between hepatobiliary cancer and typhoid carrier state // Lancet. – 1979. – Vol. 14. – P. 791–794.
72. Won Y.S., Vandamme P., Yoon J.H. et al. Helicobacter callitrichus sp. nov., a novel Helicobacter species isolated from the feces of the common marmoset (Callithrix Jacchus) // FEMS Microbiol. Lett. – 2007. – Vol. 271. – P. 239–244.
73. Wu C.S., Lin C.Y., Liaw Y.F. et al. Helicobacter pylori in cirrhotic patients with peptic ulcer disease: a prospective case-controlled study // Gastrointest. Endosc. – 1995. – Vol. 42. – P. 424–427.
74. Wu X.T., Xiao L.J., Li X.Q., Li J.S. Detection of bacterial DNA from cholesterol gallstones by tested primers polymerase chain reaction // World J. Gastroenterol. – 1998. – Vol. 4. – P. 234–237.
75. Xuan S.Y., Li N., Qiang X. et al. Helicobacter infection in hepatocellular carcinoma tissue // World J. Gastroenterol. – 2006. – Vol. 12, N 15. – P. 2335–2340.
76. Yali Z., Yamada M., Wen M. et al. Gastrospirillum hominis and Helicobacter pylori infection in Thai individuals: comparison of histopathological changes of gastric mucosa // Pathol. Int. – 1998. – Vol. 48. – P. 507–511.
77. Yang H., Goliger J.A., Song M. et al. High prevalence of Helicobacter heilmannii infection in China // Dig. Dis. Sci. – 1998. – Vol. 43. – P. 1493.
78. Young V.B., Knox A.K., Schauer D.B. Сytolethal distending toxin sequence and activity in the enterohepatic pathogen Helicobacter hepaticus // Infect. Immun. – 2000. – Vol. 68, N 1. – P. 184–191.
Рецензия
Для цитирования:
Исаева Г.Ш. Возможное участие бактерий рода Helicobacter в патогенезе гепатобилиарных заболеваний. Российский журнал гастроэнтерологии, гепатологии, колопроктологии. 2008;18(4):14-22.
For citation:
Isayeva G.Sh. Possible involvement of Helicobacter spp. bacteria in pathogenesis of hepatobiliary diseases. Russian Journal of Gastroenterology, Hepatology, Coloproctology. 2008;18(4):14-22. (In Russ.)
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