Neutrophils and tumour necrosis factor-α are important for controlling early gastrointestinal stages of experimental murine listeriosis

References

1. Farber J. M., Peterkin P. L. Listeria monocytogenes, a food-borne pathogen. Microbiol Rev 1991; 55:476–511
   [Google Scholar]
2. Miller J. K., Burns J. Histopathology of Listeria monocytogenes after oral feeding to mice. Appl Microbiol 1970; 19:772–775
   [Google Scholar]
3. MacDonald T. T., Carter P. B. Cell-mediated immunity to intestinal infection. Infect Immun 1980; 28:516–523
   [Google Scholar]
4. Okamoto M., Nakane A., Minagawa T. Host resistance to an intragastric infection with Listeria monocytogenes in mice depends on cellular immunity and intestinal bacterial flora. Infect Immun 1994; 62:3080–3085
   [Google Scholar]
5. Neutra M. R., ICraehenbuhl J.-P. Transepithelial transport and mucosal defence I: the role of M cells. Trends Cell Biol 1992; 2:134–138
   [Google Scholar]
6. Rácz P., Tenner K., Mérö E. Experimental Listeria enteritis. I. An electron microscopic study of the epithelial phase in experimental Listeria infection. Lab Invest 1972; 26:694–700
   [Google Scholar]
7. Kaufmann S. H. E. Immunity to intracellular bacteria. Annu Rev Immunol 1993; 11:129–163
   [Google Scholar]
8. Conlan J. W., North R. J. Neutrophil-mediated dissolution of infected host cells as a defense strategy against a facultative intracellular bacterium. J Exp Med 1991; 174:741–744
   [Google Scholar]
9. Conlan J. W., North R. J. Neutrophils are essential for early antiListeria defense in the liver, but not in the spleen or peritoneal cavity, as revealed by a granulocyte-depleting monoclonal antibody. J Exp Med 1994; 179:259–268
   [Google Scholar]
10. Czuprynski C. J., Brown J. F., Maroushek N., Wagner R. D., Steinberg H. Administration of anti-granulocyte mAb RB6-8C5 impairs the resistance of mice to Listeria monocytogenes infection. J Immunol 1994; 152:1836–1846
    [Google Scholar]
11. Havell E. A. Evidence that tumor necrosis factor has an important role in antibacterial resistance. J Immunol 1989; 143:2894–2899
    [Google Scholar]
12. Rogers H. W., Unanue E. R. Neutrophils are involved in acute, nonspecific resistance to Listeria monocytogenes in mice. Infect Immun 1993; 61:5090–5096
    [Google Scholar]
13. Rothe J., Lesslauer W., Lötscher H. Mice lacking the tumour necrosis factor receptor 1 are resistant to TNF-mediated toxicity but highly susceptible to infection by Listeria monocytogenes . Nature 1993; 364:798–802
    [Google Scholar]
14. Czuprynski C. J., Brown J. F. Effects of purified anti-Lyt-2 mAb treatment on murine listeriosis: comparative roles of Lyt-2⁺ and L3T4⁺ cells in resistance to primary and secondary infection, delayed-type hypersensitivity and adoptive transfer of resistance. Immunology 1990; 71:107–112
    [Google Scholar]
15. Dunn P. L., North R. J. Resolution of primary murine listeriosis and acquired resistance to lethal secondary infection can be mediated predominantly by Thy-1⁺ CD4⁻CD8⁻ cells. J Infect Dis 1991; 164:869–877
    [Google Scholar]
16. Emmerling P., Finger H., Hof H. Cell-mediated resistance to infection with Listeria monocytogenes in nude mice. Infect Immun 1977; 15:382–385
    [Google Scholar]
17. Arnold J. W., Niesel D. W., Annable C. R. Tumor necrosis factor-α mediates the early pathology in Salmonella infection of the gastrointestinal tract. Microb Pathog 1993; 14:217–227
    [Google Scholar]
18. Perdomo O. J. J., Cavaillon J. M., Huerre M., Ohayon H., Gounon P., Sansonetti P. J. Acute inflammation causes epithelial invasion and mucosal destruction in experimental shigellosis. J Exp Med 1994; 180:1307–1319
    [Google Scholar]
19. Conlan J. W., North R. J. Roles of Listeria monocytogenes virulence factors in survival: virulence factors distinct from listeriolysin are needed for the organism to survive an early neutrophil-mediated host defense mechanism. Infect Immun 1992; 60:951–957
    [Google Scholar]
20. Tepper R. l., Coffman R. L., Leder P. An eosinophil-dependent mechanism for the antitumor effect of interleukin-4. Science 1992; 257:548–551
    [Google Scholar]
21. Johnson L. L., VanderVegt F. P., Havell E. A. Gamma interferon-dependent temporary resistance to acute Toxoplasma gondii infection independent of CD4+ or CD8+ lymphocytes. Infect Immun 1993; 61:5174–5180
    [Google Scholar]
22. Dean C. J., Styles J. M., Gyure L. The production of hybridomas from the gut associated lymphoid tissue of tumour bearing rats. I. Mesenteric nodes as a source of IgG-producing cells. Clin Exp Immunol 1984; 57:358–364
    [Google Scholar]
23. Nakane A., Minagawa T., Kato K. Endogenous tumor necrosis factor (cachectin) is essential to host resistance against Listeria monocytogenes infection. Infect Immun 1988; 56:2563–2569
    [Google Scholar]
24. Garside P., Bunce C., Tomlinson R. C., Nichols B. L., Mowat A. M. Analysis of enteropathy induced by tumour necrosis factor α . Cytokine 1993; 5:24–30
    [Google Scholar]
25. Conlan J. W., North R. J. Early pathogenesis of infection in the liver with the facultative intracellular bacteria Listeria monocytogenes, Francisella tularensis, and Salmonella typhimurium involves lysis of infected hepatocytes by leukocytes. Infect Immun 1992; 60:5164–5171
    [Google Scholar]
26. Collins F. M. Immunity to enteric infection in mice. Infect Immun 1970; 1:243–250
    [Google Scholar]
27. Marco A. J., Prats N., Ramos J. A. A microbiological, histological and immunohistological study of the intragastric inoculation of Listeria monocytogenes in mice. J Comp Pathol 1992; 107:1–9
    [Google Scholar]
28. Zachar Z., Savage D. C. Microbial interference and colonization of the murine gastrointestinal tract by Listeria monocytogenes . Infect Immun 1979; 23:168–174
    [Google Scholar]
29. Conlan J. W. Early pathogenesis of Listeria monocytogenes infection in the mouse spleen. J Med Microbiol 1996; 44:295–302
    [Google Scholar]
30. Cassatella M. A. The production of cytokines by polymorphonuclear neutrophils. Immunol Today 1995; 16:21–26
    [Google Scholar]