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. 1974 Sep;27(3):501–505.

The suppression of sheep rosette-forming cells and the inability of mouse bone marrow cells to reconstitute competence after infection with the nematode Trichinella spiralis

G M Faubert, C E Tanner
PMCID: PMC1445611  PMID: 4607261

Abstract

Mice infected with the nematode Trichinella spiralis or normal mice treated either with the serum of infected animals or with a parasite extract contained fewer spleen rosette-forming cells (RFC) to sheep erythrocytes than the controls. Bone marrow cells from infected mice were considerably less efficient than normal cells in reconstituting thymectomized, irradiated animals.

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Selected References

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

  1. Biozzi G., Stiffel C., Mouton D., Liacopoulosbriot M., Decreusefond C., Bouthillier Y. Etude du phénomène de l'immuno-cyto-adhérence au cours de l'immunisation. Ann Inst Pasteur (Paris) 1966 Mar;110(3 Suppl):7–32. [PubMed] [Google Scholar]
  2. Bomford R., Wedderburn N. Depression of immune response to Moloney leukaemia virus by malarial infection. Nature. 1973 Apr 13;242(5398):471–473. doi: 10.1038/242471a0. [DOI] [PubMed] [Google Scholar]
  3. Cypess R. H., Lubiniecki A. S., Hammon W. M. Immunosuppression and increased susceptibility to Japaneses B encephalitis virus in Trichinella spiralis-infected mice. Proc Soc Exp Biol Med. 1973 Jun;143(2):469–473. doi: 10.3181/00379727-143-37345. [DOI] [PubMed] [Google Scholar]
  4. Faubert G., Tanner C. E. Trichinella spiralis: inhibition of sheep hemagglutinins in mice. Exp Parasitol. 1971 Aug;30(1):120–123. doi: 10.1016/0014-4894(71)90077-4. [DOI] [PubMed] [Google Scholar]
  5. Greaves M. F., Möller E. Studies on antigen-binding cells. I. The origin of reactive cells. Cell Immunol. 1970 Oct;1(4):372–385. doi: 10.1016/0008-8749(70)90015-8. [DOI] [PubMed] [Google Scholar]
  6. Huldt G., Gard S., Olovson S. G. Effect of Toxoplasma gondii on the thymus. Nature. 1973 Aug 3;244(5414):301–303. doi: 10.1038/244301a0. [DOI] [PubMed] [Google Scholar]
  7. Larsh J. E., Jr, Goulson H. T., Weatherly N. F., Chaffee E. F. Studies on delayed (cellular) hypersensitivity in mice infected with Trichinella spiralis. VI. Results in recipients injected with antiserum or "freeze-thaw" spleen cells. J Parasitol. 1970 Dec;56(6):1206–1209. [PubMed] [Google Scholar]
  8. Larsh J. E., Jr, Race G. J., Goulson H. T., Weatherly N. F. Studies on delayed (cellular) hypersensitivity in mice infected with Trichinella spiralis. 3. Serologic and histopathologic findings in recipients given peritoneal exudate cells. J Parasitol. 1966 Feb;52(1):146–156. [PubMed] [Google Scholar]
  9. Svet-Moldavsky G. J., Shaghijan G. S., Chernyakhovskaya I. Y., Mkheidze D. M., Litovchenko T. A., Ozeretskovskaya N. N., Kadaghidze Z. G. Inhibition of skin allograft rejection in trichinella-infected mice. Transplantation. 1970 Jan;9(1):69–71. doi: 10.1097/00007890-197001000-00020. [DOI] [PubMed] [Google Scholar]
  10. Tanner C. E. Immunochemical study of the antigens of Trichinella spiralis larvae. IV. Purification by continuous-flow paper electrophoresis and column chromatography. Exp Parasitol. 1970 Feb;27(1):116–135. doi: 10.1016/s0014-4894(70)80016-9. [DOI] [PubMed] [Google Scholar]
  11. Walls R. S., Carter R. L., Leuchars E., Davies A. J. The immunopathology of trichiniasis in T-cell deficient mice. Clin Exp Immunol. 1973 Feb;13(2):231–242. [PMC free article] [PubMed] [Google Scholar]

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