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. 1973 Mar;13(3):467–478.

The immunological significance of histological changes in the spleen and liver in mouse malaria

C J Moran, Violeta S de Rivera, J L Turk
PMCID: PMC1553769  PMID: 4573765

Abstract

The spleens and livers of mice were investigated histologically on various days subsequent to infection with Plasmodium berghei yoelii using immunofluorescence and autoradiography. At the height of the parasitaemia, at a time when nonspecific immunosuppression is known to occur, the `thymus-dependent area' round the central arteriole of the spleen was replaced by proliferating lymphoid cells many of which were IgG containing plasmablasts. There was also at this time a considerable decrease in small lymphocytes in this area. The significance of these findings is discussed in relation to the non-specific immunosuppression. In addition evidence for immune complex deposition was obtained in a number of tissues.

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Selected References

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  1. Greenwood B. M., Brown J. C., De Jesus D. G., Holborow E. J. Immunosuppression in murine malaria. II. The effect on reticulo-endothelial and germinal centre function. Clin Exp Immunol. 1971 Sep;9(3):345–354. [PMC free article] [PubMed] [Google Scholar]
  2. Ironside P. N. Production of anti-human-globulin in goats. Immunology. 1968 Oct;15(4):503–507. [PMC free article] [PubMed] [Google Scholar]
  3. Landau I., Killick-Kendrick R. Rodent plasmodia of the République Centrafricaine: the sporogony and tissue stages of Plasmodium chabaudi and P. berghei yoelii. Trans R Soc Trop Med Hyg. 1966;60(5):633–649. doi: 10.1016/0035-9203(66)90010-1. [DOI] [PubMed] [Google Scholar]
  4. Lowenthal M. N., O'Riordan E. C., Hutt M. S. Tropical splenomegaly syndrome in Zambia: further observations and effects of cycloguanil and proguanil. Br Med J. 1971 Feb 20;1(5746):429–432. doi: 10.1136/bmj.1.5746.429. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Marsden P. D., Connor D. H., Voller A., Kelly A., Schofield F. D., Hutt M. S. Splenomegaly in New Guinea. Bull World Health Organ. 1967;36(6):901–911. [PMC free article] [PubMed] [Google Scholar]
  6. PELC S. R. The stripping-film technique of autoradiography. Int J Appl Radiat Isot. 1956 Nov;1(3):172–177. doi: 10.1016/0020-708x(56)90003-5. [DOI] [PubMed] [Google Scholar]
  7. Parrott D. V., De Sousa M. A., East J. Thymus-dependent areas in the lymphoid organs of neonatally thymectomized mice. J Exp Med. 1966 Jan 1;123(1):191–204. doi: 10.1084/jem.123.1.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Salaman M. H., Wedderburn N., Bruce-Chwatt L. J. The immunodepressive effect of a murine plasmodium and its interaction with murine oncogenic viruses. J Gen Microbiol. 1969 Dec;59(3):383–391. doi: 10.1099/00221287-59-3-383. [DOI] [PubMed] [Google Scholar]
  9. Stecher V. J., Thorbecke G. J. Beta-1C and immune globulin formation in vitro by tissues from germ-free and conventional rodents of various ages. Immunology. 1967 Apr;12(4):475–487. [PMC free article] [PubMed] [Google Scholar]

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