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. 1988 Oct;56(10):2766–2768. doi: 10.1128/iai.56.10.2766-2768.1988

Effect of the gastrointestinal microflora on induction and maintenance of oral tolerance to ovalbumin in C3H/HeJ mice.

M C Moreau 1, G Corthier 1
PMCID: PMC259643  PMID: 3417356

Abstract

The effect of the digestive microflora on oral tolerance to ovalbumin was studied by using axenic (germfree) and conventional C3H/HeJ mice. In contrast to reported results of studies with sheep erythrocytes, oral administration of ovalbumin induced tolerance in axenic mice, but the maintenance of tolerance was found to be of shorter duration than was with conventional mice. These data indicate that the contribution of the microflora to oral tolerance depends on the antigen used.

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Selected References

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  1. Bos N. A., Meeuwsen C. G., Hooijkaas H., Benner R., Wostmann B. S., Pleasants J. R. Early development of Ig-secreting cells in young of germ-free BALB/c mice fed a chemically defined ultrafiltered diet. Cell Immunol. 1987 Mar;105(1):235–245. doi: 10.1016/0008-8749(87)90071-2. [DOI] [PubMed] [Google Scholar]
  2. Elson C. O. Induction and control of the gastrointestinal immune system. Scand J Gastroenterol Suppl. 1985;114:1–15. doi: 10.3109/00365528509093764. [DOI] [PubMed] [Google Scholar]
  3. Endres R. O., Grey H. M. Antigen recognition by T cells. II. Intravenous administration of native or denatured ovalbumin results in tolerance to both forms of the antigen. J Immunol. 1980 Oct;125(4):1521–1525. [PubMed] [Google Scholar]
  4. Guy-Grand D., Griscelli C., Vassalli P. The gut-associated lymphoid system: nature and properties of the large dividing cells. Eur J Immunol. 1974 Jun;4(6):435–443. doi: 10.1002/eji.1830040610. [DOI] [PubMed] [Google Scholar]
  5. Jarrett E. E. Immunoregulation of IgE responses: the role of the gut in perspective. Ann Allergy. 1984 Dec;53(6 Pt 2):550–556. [PubMed] [Google Scholar]
  6. Kiyono H., McGhee J. R., Wannemuehler M. J., Michalek S. M. Lack of oral tolerance in C3H/HeJ mice. J Exp Med. 1982 Feb 1;155(2):605–610. doi: 10.1084/jem.155.2.605. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Mattingly J. A., Kaplan J. M., Janeway C. A., Jr Two distinct antigen-specific suppressor factors induced by the oral administration of antigen. J Exp Med. 1980 Sep 1;152(3):545–554. doi: 10.1084/jem.152.3.545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Mattingly J. A., Waksman B. H. Immunologic suppression after oral administration of antigen. I. Specific suppressor cells formed in rat Peyer's patches after oral administration of sheep erythrocytes and their systemic migration. J Immunol. 1978 Nov;121(5):1878–1883. [PubMed] [Google Scholar]
  9. Michalek S. M., Kiyono H., Wannemuehler M. J., Mosteller L. M., McGhee J. R. Lipopolysaccharide (LPS) regulation of the immune response: LPS influence on oral tolerance induction. J Immunol. 1982 May;128(5):1992–1998. [PubMed] [Google Scholar]
  10. Moreau M. C., Raibaud P., Muller M. C. Relation entre le développement du système immunitaire intestinal à IgA et l'établissement de la flore microbienne dans le tube digestif du souriceau holoxénique. Ann Immunol (Paris) 1982 Jul-Aug;133D(1):29–39. [PubMed] [Google Scholar]
  11. Mowat A. M., Thomas M. J., MacKenzie S., Parrott D. M. Divergent effects of bacterial lipopolysaccharide on immunity to orally administered protein and particulate antigens in mice. Immunology. 1986 Aug;58(4):677–683. [PMC free article] [PubMed] [Google Scholar]
  12. Ngan J., Kind L. S. Suppressor T cells for IgE and IgG in Peyer's patches of mice made tolerant by the oral administration of ovalbumin. J Immunol. 1978 Mar;120(3):861–865. [PubMed] [Google Scholar]
  13. Richman L. K., Chiller J. M., Brown W. R., Hanson D. G., Vaz N. M. Enterically induced immunologic tolerance. I. Induction of suppressor T lymphoyctes by intragastric administration of soluble proteins. J Immunol. 1978 Dec;121(6):2429–2434. [PubMed] [Google Scholar]
  14. Saklayen M. G., Pesce A. J., Pollak V. E., Michael J. G. Induction of oral tolerance in mice unresponsive to bacterial lipopolysaccharide. Infect Immun. 1983 Sep;41(3):1383–1385. doi: 10.1128/iai.41.3.1383-1385.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Schutze M. P., Leclerc C., Vogel F. R., Chedid L. Epitopic suppression in synthetic vaccine models: analysis of the effector mechanisms. Cell Immunol. 1987 Jan;104(1):79–90. doi: 10.1016/0008-8749(87)90008-6. [DOI] [PubMed] [Google Scholar]
  16. Strobel S., Ferguson A. Persistence of oral tolerance in mice fed ovalbumin is different for humoral and cell-mediated immune responses. Immunology. 1987 Feb;60(2):317–318. [PMC free article] [PubMed] [Google Scholar]
  17. Tlaskalová-Hogenová H., Sterzl J., Stepánkova R., Dlabac V., Veticka V., Rossmann P., Mandel L., Rejnek J. Development of immunological capacity under germfree and conventional conditions. Ann N Y Acad Sci. 1983 Jun 30;409:96–113. doi: 10.1111/j.1749-6632.1983.tb26862.x. [DOI] [PubMed] [Google Scholar]
  18. Vaz N. M., Maia L. C., Hanson D. G., Lynch J. M. Inhibition of homocytotropic antibody responses in adult inbred mice by previous feeding of the specific antigen. J Allergy Clin Immunol. 1977 Aug;60(2):110–115. doi: 10.1016/0091-6749(77)90035-5. [DOI] [PubMed] [Google Scholar]
  19. Wannemuehler M. J., Kiyono H., Babb J. L., Michalek S. M., McGhee J. R. Lipopolysaccharide (LPS) regulation of the immune response: LPS converts germfree mice to sensitivity to oral tolerance induction. J Immunol. 1982 Sep;129(3):959–965. [PubMed] [Google Scholar]

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