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. 1973 Jan 31;137(2):239–253. doi: 10.1084/jem.137.2.239

SYNERGY AMONG LYMPHOID CELLS MEDIATING THE GRAFT-VERSUS-HOST RESPONSE

V. DERIVATION BY MIGRATION IN LETHALLY IRRADIATED RECIPIENTS OF TWO INTERACTING SUBPOPULATIONS OF THYMUS-DERIVED CELLS FROM NORMAL SPLEEN

Robert E Tigelaar 1, Richard Asofsky 1
PMCID: PMC2139477  PMID: 4405532

Abstract

Spleen cells from normal adult mice were injected into lethally irradiated adult syngeneic recipients. 24 h later, cell suspensions were prepared from the recipients' spleens or peripheral lymph nodes and tested either alone or combined for their capacity to elicit graft-versus-host (GVH) reactions in neonatal F1 recipients, using the Simonsen spleen weight assay. Either the lymph node-seeking subpopulation or the spleen-seeking subpopulation alone was markedly deficient in its ability to provide a GVH reaction when compared with the normal population from which it was derived. However, an appropriate mixture of the two had a reactivity characteristic of the parent population. Both subpopulations were sensitive to treatment with anti-θ antibody and complement in vitro. These results provide a convincing demonstration of the functional heterogeneity within the pool of thymus-derived cells present in a single normal lymphoid tissue. They strongly suggest that the normal expression of GVH reactivity of such a tissue involves an interaction among distinct subpopulations of thymus-derived cells.

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Selected References

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

  1. Baird S., Santa J., Weissman I. Anti-theta antisera may contain anti-allotype contamination. Nat New Biol. 1971 Jul 14;232(28):56–56. doi: 10.1038/newbio232056a0. [DOI] [PubMed] [Google Scholar]
  2. Baker P. J., Stashak P. W., Amsbaugh D. F., Prescott B., Barth R. F. Evidence for the existence of two functionally distinct types of cells which regulate the antibody response to type 3 pneumococcal polysaccharide. J Immunol. 1970 Dec;105(6):1581–1583. [PubMed] [Google Scholar]
  3. Barchilon J., Gershon R. K. Synergism between thymocytes and bone marrow cells in a graft versus host reaction. Nature. 1970 Jul 4;227(5253):71–72. doi: 10.1038/227071a0. [DOI] [PubMed] [Google Scholar]
  4. Bianco C., Nussenzweig V. Theta-bearing and complement-receptor lymphocytes are distinct populations of cells. Science. 1971 Jul 9;173(3992):154–156. doi: 10.1126/science.173.3992.154. [DOI] [PubMed] [Google Scholar]
  5. Cantor H., Asofsky R. Synergy among lymphoid cells mediating the graft-versus-host response. 3. Evidence for interaction between two types of thymus-derived cells. J Exp Med. 1972 Apr 1;135(4):764–779. doi: 10.1084/jem.135.4.764. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. 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]
  7. Cantor H. Differential migration of helper and precursor spleen cells following immunization. Eur J Immunol. 1971 Dec;1(6):462–464. doi: 10.1002/eji.1830010611. [DOI] [PubMed] [Google Scholar]
  8. Cantor H. The effects of anti-theta antiserum upon graft-versus-host activity of spleen and lymph node cells. Cell Immunol. 1972 Mar;3(3):461–469. doi: 10.1016/0008-8749(72)90251-1. [DOI] [PubMed] [Google Scholar]
  9. Claman H. N., Chaperon E. A. Immunologic complementation between thymus and marrow cells--a model for the two-cell theory of immunocompetence. Transplant Rev. 1969;1:92–113. doi: 10.1111/j.1600-065x.1969.tb00137.x. [DOI] [PubMed] [Google Scholar]
  10. Claman H. N., Chaperon E. A., Triplett R. F. Thymus-marrow cell combinations. Synergism in antibody production. Proc Soc Exp Biol Med. 1966 Aug-Sep;122(4):1167–1171. doi: 10.3181/00379727-122-31353. [DOI] [PubMed] [Google Scholar]
  11. Davies A. J. The thymus and the cellular basis of immunity. Transplant Rev. 1969;1:43–91. doi: 10.1111/j.1600-065x.1969.tb00136.x. [DOI] [PubMed] [Google Scholar]
  12. Dennert G., Lennox E. Cell interactions in humoral and cell-mediated immunity. Nat New Biol. 1972 Jul 26;238(82):114–116. doi: 10.1038/newbio238114a0. [DOI] [PubMed] [Google Scholar]
  13. GOWANS J. L., KNIGHT E. J. THE ROUTE OF RE-CIRCULATION OF LYMPHOCYTES IN THE RAT. Proc R Soc Lond B Biol Sci. 1964 Jan 14;159:257–282. doi: 10.1098/rspb.1964.0001. [DOI] [PubMed] [Google Scholar]
  14. Gershon R. K., Cohen P., Hencin R., Liebhaber S. A. Suppressor T cells. J Immunol. 1972 Mar;108(3):586–590. [PubMed] [Google Scholar]
  15. Gershon R. K., Liebhaber S. A. The response of T cells to histocompatibility-2 antigens. Dose-response kinetics. J Exp Med. 1972 Jul 1;136(1):112–127. doi: 10.1084/jem.136.1.112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hilgard H. R. Dissociation of splenomegaly from graft-versus-host disease by host x-irradiation. Transplantation. 1970 Nov;10(5):396–402. doi: 10.1097/00007890-197011000-00006. [DOI] [PubMed] [Google Scholar]
  17. 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]
  18. Katz D. H., Paul W. E., Goidl E. A., Benacerraf B. Radioresistance of cooperative function of carrier-specific lymphocytes in antihapten antibody responses. Science. 1970 Oct 23;170(3956):462–464. doi: 10.1126/science.170.3956.462. [DOI] [PubMed] [Google Scholar]
  19. Kettman J., Dutton R. W. Radioresistance of the enhancing effect of cells from carrier-immunized mice in an in vitro primary immune response. Proc Natl Acad Sci U S A. 1971 Apr;68(4):699–703. doi: 10.1073/pnas.68.4.699. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Lance E. M., Taub R. N. Segregation of lymphocyte populations through differential migration. Nature. 1969 Mar 1;221(5183):841–843. doi: 10.1038/221841a0. [DOI] [PubMed] [Google Scholar]
  21. Mandel M. A., Asofsky R. The effects of heterologous anti-thymocyte sera in mice. 3. High susceptibility of germfree mice to the suppressive effects of IgG from rabbit anti-mouse thymocyte serum. J Exp Med. 1969 Jun 1;129(6):1203–1216. doi: 10.1084/jem.129.6.1203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Miller J. F., Mitchell G. F. Thymus and antigen-reactive cells. Transplant Rev. 1969;1:3–42. doi: 10.1111/j.1600-065x.1969.tb00135.x. [DOI] [PubMed] [Google Scholar]
  23. Mosier D. E., Coppleson L. W. A THREE-CELL INTERACTION REQUIRED FOR THE INDUCTION OF THE PRIMARY IMMUNE RESPONSE in vitro. Proc Natl Acad Sci U S A. 1968 Oct;61(2):542–547. doi: 10.1073/pnas.61.2.542. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Okumura K., Tada T. Regulation of homocytotropic antibody formation in the rat. VI. Inhibitory effect of thymocytes on the homocytotropic antibody response. J Immunol. 1971 Dec;107(6):1682–1689. [PubMed] [Google Scholar]
  25. 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]
  26. 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]
  27. SIMONSEN M. Graft versus host reactions. Their natural history, and applicability as tools of research. Prog Allergy. 1962;6:349–467. [PubMed] [Google Scholar]
  28. Taub R. N., Lance E. M. Effects of heterologous anti-lymphocyte serum on the distribution of 51-Cr-labelled lymph node cells in mice. Immunology. 1968 Nov;15(5):633–642. [PMC free article] [PubMed] [Google Scholar]
  29. Taub R. N., Lance E. M. Effects of lymphoid depletion on the distribution of 51Cr-labeled lymph node cells in mice. Transplantation. 1971 Jun;11(6):536–542. [PubMed] [Google Scholar]
  30. Taylor R. B. Cellular cooperation in the antibody response of mice to two serum albumins: specific function of thymus cells. Transplant Rev. 1969;1:114–149. doi: 10.1111/j.1600-065x.1969.tb00138.x. [DOI] [PubMed] [Google Scholar]
  31. Tigelaar R. E., Asofsky R. Synergy among lymphoid cells mediating the graft-versus-host response. IV. Synergy in the GVH reaction quantitated by a mortality assay in sublethally irradiated recipients. J Exp Med. 1972 May 1;135(5):1059–1070. doi: 10.1084/jem.135.5.1059. [DOI] [PMC free article] [PubMed] [Google Scholar]

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