Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1974 Jul 1;140(1):296–299. doi: 10.1084/jem.140.1.296

SYSTEMIC CELLULAR HYPERSENSITIVITY INDUCED BY AN INTESTINALLY ABSORBED ANTIGEN

Joseph L Perrotto 1, Le Ming Hang 1, K J Isselbacher 1, K S Warren 1
PMCID: PMC2139700  PMID: 4857866

Abstract

Neonatal mice given intact living Schistosoma mansoni eggs or soluble schistosome egg antigens intragastrically developed systemic cellular hypersensitivity as shown by markedly accelerated, augmented granulomatous inflammation around S. mansoni eggs subsequently injected intravenously into the pulmonary microvasculature. To achieve partial sensitization in adult mice schistosome eggs had to be administered intragastrically with bicarbonate; full sensitization occurred when the eggs were injected intraduodenally. These data indicate that under appropriate conditions intestinal administration of antigen can result in systemic cellular immune sensitization.

Full Text

The Full Text of this article is available as a PDF (214.7 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bernstein I. D., Ovary Z. Absorption of antigens from the gastrointestinal tract. Int Arch Allergy Appl Immunol. 1968;33(6):521–527. doi: 10.1159/000230068. [DOI] [PubMed] [Google Scholar]
  2. Boros D. L., Warren K. S. Delayed hypersensitivity-type granuloma formation and dermal reaction induced and elicited by a soluble factor isolated from Schistosoma mansoni eggs. J Exp Med. 1970 Sep 1;132(3):488–507. doi: 10.1084/jem.132.3.488. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. COKER C. M., LICHTENBERG F. A revised method for isolation of Schistosoma mansoni eggs for biological experimentation. Proc Soc Exp Biol Med. 1956 Aug-Sep;92(4):780–782. doi: 10.3181/00379727-92-22612. [DOI] [PubMed] [Google Scholar]
  4. Dineen J. K., Adams D. B. The role of the recirculating thymus-dependent lymphocyte in resistance to Trichostrongylus colubriformis in the guinea-pig. Immunology. 1971 Jan;20(1):109–113. [PMC free article] [PubMed] [Google Scholar]
  5. Ogra P. L., Karzon D. T. Distribution of poliovirus antibody in serum, nasopharynx and alimentary tract following segmental immunization of lower alimentary tract with poliovaccine. J Immunol. 1969 Jun;102(6):1423–1430. [PubMed] [Google Scholar]
  6. Rothberg R. M., Kraft S. C., Michalek S. M. Systemic immunity after local antigenic stimulation of the lymphoid tissue of the gastrointestinal tract. J Immunol. 1973 Dec;111(6):1906–1913. [PubMed] [Google Scholar]
  7. Uhr J. W. Delayed hypersensitivity. Physiol Rev. 1966 Jul;46(3):359–419. doi: 10.1152/physrev.1966.46.3.359. [DOI] [PubMed] [Google Scholar]
  8. Walker W. A., Cornell R., Davenport L. M., Isselbacher K. J. Macromolecular absorption. Mechanism of horseradish peroxidase uptake and transport in adult and neonatal rat intestine. J Cell Biol. 1972 Aug;54(2):195–205. doi: 10.1083/jcb.54.2.195. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Warren K. S., Domingo E. O., Cowan R. B. Granuloma formation around schistosome eggs as a manifestation of delayed hypersensitivity. Am J Pathol. 1967 Nov;51(5):735–756. [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES