Abstract
Mice were treated with sublethal and midlethal doses of irradiation (500–700 rads) and injected intravenously with allogeneic or semiallogeneic F1 hybrid spleen cells. The cytotoxicity developed by their spleen cells was measured with the lysis of 51Cr-labeled target cells and was found to be stronger (although delayed in time) than the cytotoxic activity of spleen cells from nonirradiated mice. The injection of syngeneic thymus or spleen cells in the irradiated mice after their treatment with allogeneic spleen cells exerted a suppressor activity, i.e., reduced the level of cell-mediated cytotoxicity (CMC). The majority of effector cells involved in the modified CMC response of irradiated mice was shown to be of host origin and lysed specifically target cells of the same genotype as the donor. A small percentage of the cells obtained from the spleens of irradiated recipients of allogeneic spleen cells was composed of donor cells which lysed specifically target cells of the same genotype as the host. These results demonstrate that the precursors of the cytotoxic cells responsible for target cell lysis are relatively radioresistant and suggest that their response is regulated by radiosensitive thymus-dependent cells.
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Selected References
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- 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]
- Chen C. H., Sabbadini E., Sehon A. H. Specificity of xenoantisera against mouse cell surface antigens. Transplantation. 1974 Jan 1;17(1):22–29. doi: 10.1097/00007890-197401000-00005. [DOI] [PubMed] [Google Scholar]
- Cohen A., Schlesinger M. Absorption of guinea pig serum with agar. A method for elimination of itscytotoxicity for murine thymus cells. Transplantation. 1970 Jul;10(1):130–132. doi: 10.1097/00007890-197007000-00027. [DOI] [PubMed] [Google Scholar]
- Evans R., Alexander P. Mechanism of immunologically specific killing of tumour cells by macrophages. Nature. 1972 Mar 24;236(5343):168–170. doi: 10.1038/236168a0. [DOI] [PubMed] [Google Scholar]
- Gershon R. K., Cohen P., Hencin R., Liebhaber S. A. Suppressor T cells. J Immunol. 1972 Mar;108(3):586–590. [PubMed] [Google Scholar]
- Grant C. K., Currie G. A., Alexander P. Thymocytes from mice immunized against an allograft render bone-marrow cells specifically cytotoxic. J Exp Med. 1972 Jan;135(1):150–164. doi: 10.1084/jem.135.1.150. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Manyko V. M. Effect of radiation on lymphocytes: abolition of the phenomenon of allogeneic stem. Cell inactivation. Folia Biol (Praha) 1971;17(6):365–369. [PubMed] [Google Scholar]
- Singh J. N., Sabbadini E., Sehon A. H. Detection of nonspecific cytotoxicity in graft-versus-host reaction as a function of target cell type. Cell Immunol. 1973 Aug;8(2):280–289. doi: 10.1016/0008-8749(73)90117-2. [DOI] [PubMed] [Google Scholar]
- Sprent J., Miller J. F. Interaction of thymus lymphocytes with histoincompatible cells. 3. Immunological characteristics of recirculating lymphocytes derived from activated thymus cells. Cell Immunol. 1972 Feb;3(2):213–230. doi: 10.1016/0008-8749(72)90161-x. [DOI] [PubMed] [Google Scholar]
- Stobo J. D., Paul W. E., Henney C. S. Functional heterogeneity of murine lymphoid cells. IV. Allogeneic mixed lymphocyte reactivity and cytolytic activity as functions of distinct T cell subsets. J Immunol. 1973 Mar;110(3):652–660. [PubMed] [Google Scholar]
- Wagner H. Synergy during in vitro cytotoxic allograft responses. I. Evidence for cell interaction between thymocytes and peripheral T cells. J Exp Med. 1973 Dec 1;138(6):1379–1397. doi: 10.1084/jem.138.6.1379. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zan-Bar I., Nachtigal D., Feldman M. Mechanisms in immune tolerance. I. A specific block of immunological memory in HSA-tolerant mice. Cell Immunol. 1974 Jan;10(1):19–30. doi: 10.1016/0008-8749(74)90147-6. [DOI] [PubMed] [Google Scholar]
