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. 1972 Oct;45(5):519–529.

Significance of cell interactions in production of graft versus host splenomegaly.

J Barchilon, S A Liebhaber, R K Gershon
PMCID: PMC2591870  PMID: 4404559

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Selected References

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

  1. Cantor H., Asofsky R. Synergy among lymphoid cells mediating the graft-versus-host response. II. Synergy in graft-versus-host reactions produced by Balb-c lymphoid cells of differing anatomic origin. J Exp Med. 1970 Feb;131(2):235–246. doi: 10.1084/jem.131.2.235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cantor H., Asofsky R., Talal N. Synergy among lymphoid cells mediating the graft-versus-host response. I. Synergy in graft-versus-host reactions produced by cells from NZB-Bl mice. J Exp Med. 1970 Feb;131(2):223–234. doi: 10.1084/jem.131.2.223. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. DAVIES A. J., DOAK S. M. Fate of homologous adult spleen cells injected into new-born mice. Nature. 1960 Aug 13;187:610–611. doi: 10.1038/187610b0. [DOI] [PubMed] [Google Scholar]
  4. Gershon R. K., Kondo K. Cell interactions in the induction of tolerance: the role of thymic lymphocytes. Immunology. 1970 May;18(5):723–737. [PMC free article] [PubMed] [Google Scholar]
  5. HOWARD J. G., MICHIE D., SIMONSEN M. Splenomegaly as a host response in graft-versus-host disease. Br J Exp Pathol. 1961 Oct;42:478–485. [PMC free article] [PubMed] [Google Scholar]
  6. Hilgard H. R. Synergism of thymus and bone marrow in the production of gra a5hilgard HR: Synergism of thymus and bone marrow in the production of graft-versus-host splenomegaly in x-irradiated hosts. J Exp Med. 1970 Aug 1;132(2):317–328. doi: 10.1084/jem.132.2.317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lubaroff D. M., Waksman B. H. Bone marrow as a source of cells in reactions of cellular hypersensitivity. I. Passive transfer of tuberculin sensitivity in syngeneic systems. J Exp Med. 1968 Dec 1;128(6):1425–1435. doi: 10.1084/jem.128.6.1425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. McCullagh P. J. The abrogation of sheep erythrocyte tolerance in rats by means of the transfer of allogeneic lymphocytes. J Exp Med. 1970 Nov;132(5):916–925. doi: 10.1084/jem.132.5.916. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Nakić B., Kastelan A., Mikuska J., Bunarević A. Quantitative analysis of the chimaeric state in mice. II. Cytological examination of the proportion of proliferating donor and host cells in runt disease in mice. Immunology. 1967 Jun;12(6):615–627. [PMC free article] [PubMed] [Google Scholar]
  10. REIF A. E., ALLEN J. M. THE AKR THYMIC ANTIGEN AND ITS DISTRIBUTION IN LEUKEMIAS AND NERVOUS TISSUES. J Exp Med. 1964 Sep 1;120:413–433. doi: 10.1084/jem.120.3.413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Raff M. Evidence for subpopulation of mature lymphocytes within mouse thymus. Nat New Biol. 1971 Feb 10;229(6):182–184. doi: 10.1038/newbio229182a0. [DOI] [PubMed] [Google Scholar]
  12. Taylor H. D. BLOOD COUNTS IN EXPERIMENTAL POLIOMYELITIS IN THE MONKEY. J Exp Med. 1919 Jan 1;29(1):97–114. doi: 10.1084/jem.29.1.97. [DOI] [PMC free article] [PubMed] [Google Scholar]

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