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. 1982 Nov;38(2):521–529. doi: 10.1128/iai.38.2.521-529.1982

Genetic control of cell-mediated immunity in rats: involvement of RT1.B locus determinants in the proliferative response of T lymphocytes to Listeria antigens.

T W Jungi, R Jungi
PMCID: PMC347769  PMID: 6128307

Abstract

The cellular requirements for Listeria monocytogenes antigen-induced, specific [3H]thymidine incorporation into lymphoid cells were analysed. Nylon-nonadherent lymph node and peritoneal exudate cells from infected athymic rats and mice failed to respond by proliferation, whereas control cells of thymus-bearing animals gave significant responses. In mice, cells expressing Thy-1 at a high density were required for the initiation of the proliferative response, but cells with lower density also participated in proliferation. Immune T cells alone failed to respond to L. monocytogenes antigen, but the addition of accessory cells provided optimal responses. These were nylon wool adherent, absent from thoracic duct lymph, but present in thymus and lymph nodes and particularly abundant in spleens of nonimmune rats. Accessory cells had to be matched at the B region of RT1, the major histocompatibility complex, to provide a stimulatory signal for L. monocytogenes antigen-specific T cells. Thus, the genetic restriction criteria were the same as for the transfer of delayed-type hypersensitivity to L. monocytogenes antigen, but differed from those controlling the transfer of acquired cellular resistance. The interaction between T cells and accessory cells could be blocked by alloantisera directed against Ia-antigens expressed on the accessory cell population. The study suggests that killed L. monocytogenes bacteria are presented by Ia-positive adherent cells in a RT1.B-restricted fashion to provide a proliferative signal for sensitized T cells.

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Selected References

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  1. Bergholtz B. O., Thorsby E. HLA-D restriction of the macrophage-dependent response of immune human T lymphocytes to PPD in vitro: inhibition by anti-HLA-DR antisera. Scand J Immunol. 1978;8(1):63–73. doi: 10.1111/j.1365-3083.1978.tb00496.x. [DOI] [PubMed] [Google Scholar]
  2. Bergholtz B. O., Thorsby E. Macrophage-dependent response of immune human T lymphocytes to PPD in vitro. Influence of HLA-D histocompatibility. Scand J Immunol. 1977;6(8):779–786. doi: 10.1111/j.1365-3083.1977.tb02151.x. [DOI] [PubMed] [Google Scholar]
  3. Cheers C., Waller R. Activated macrophages in congenitally athymic "nude mice" and in lethally irradiate mice. J Immunol. 1975 Sep;115(3):844–847. [PubMed] [Google Scholar]
  4. Emmerling P., Finger H., Hof H. Cell-mediated resistance to infection with Listeria monocytogenes in nude mice. Infect Immun. 1977 Feb;15(2):382–385. doi: 10.1128/iai.15.2.382-385.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Farr A. G., Kiely J. M., Unanue E. R. Macrophage-T cell interactions involving Listeria monocytogenes--role of the H-2 gene complex. J Immunol. 1979 Jun;122(6):2395–2404. [PubMed] [Google Scholar]
  6. Holmberg L. A., Springer T. A., Ault K. A. Natural killer activity in the peritoneal exudates of mice infected with Listeria monocytogenes: characterization of the natural killer cells by using a monoclonal rat anti-murine macrophage antibody (M1/70). J Immunol. 1981 Nov;127(5):1792–1799. [PubMed] [Google Scholar]
  7. Jungi T. W. Immunological memory to Listeria monocytogenes in rodents: evidence for protective T lymphocytes outside the recirculating lymphocyte pool. J Reticuloendothel Soc. 1980 Oct;28(4):405–417. [PubMed] [Google Scholar]
  8. Jungi T. W. Immunological memory to listeria monocytogenes in rodents: assessment of acquired resistance in testes and comparison with delayed-type hypersensitivity. J Reticuloendothel Soc. 1981 Jul;30(1):33–45. [PubMed] [Google Scholar]
  9. Jungi T. W. In vitro proliferation of T lymphocytes from Listeria-infected rodents: assay conditions for rat peritoneal exudate cells and characterization of an inhibitor. Infect Immun. 1980 Dec;30(3):741–752. doi: 10.1128/iai.30.3.741-752.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Jungi T. W., Kunz H. W., Gill T. J., 3rd Genetic control of cell-mediated immunity in the rat. I. Transfer of DTH to bacterial antigens is restricted by the B region of RT1. J Immunogenet. 1981 Oct;8(5):345–356. doi: 10.1111/j.1744-313x.1981.tb00939.x. [DOI] [PubMed] [Google Scholar]
  11. Jungi T. W., Kunz H. W., Gill T. J., 3rd, McGregor D. D. Genetic constraints for transfer of acquired resistance and delayed-type hypersensitivity to Listeria monocytogenes in the rat. Transplant Proc. 1981 Jun;13(2):1383–1389. [PubMed] [Google Scholar]
  12. Jungi T. W., McGregor D. D. Allogeneic restriction in the rat: genetic basis of restriction of the T cell mediators of delayed-type hypersensitivity and antimicrobial resistance to Listeria monocytogenes. J Immunogenet. 1980 Jun;7(3):243–260. doi: 10.1111/j.1744-313x.1980.tb00934.x. [DOI] [PubMed] [Google Scholar]
  13. Jungi T. W., McGregor D. D. Allogeneic restriction of acquired antimicrobial resistance in the rat. J Immunol. 1978 Aug;121(2):449–455. [PubMed] [Google Scholar]
  14. Jungi T. W., McGregor D. D. Allogeneic restriction of the delayed inflammatory reaction in the rat. J Immunol. 1978 Aug;121(2):456–463. [PubMed] [Google Scholar]
  15. Jungi T. W., McGregor D. D. Generation of macrophage chemotactic activity in situ in Listeria-immune rats. Cell Immunol. 1977 Oct;33(2):322–339. doi: 10.1016/0008-8749(77)90162-9. [DOI] [PubMed] [Google Scholar]
  16. Kaufmann S. H., Simon M. M., Hahn H. Specific Lyt 123 cells are involved in protection against Listeria monocytogenes and in delayed-type hypersensitivity to listerial antigens. J Exp Med. 1979 Oct 1;150(4):1033–1038. doi: 10.1084/jem.150.4.1033. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Mackaness G. B. The influence of immunologically committed lymphoid cells on macrophage activity in vivo. J Exp Med. 1969 May 1;129(5):973–992. doi: 10.1084/jem.129.5.973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. McGregor D. D., Koster F. T., Mackaness G. B. The mediator of cellular immunity. I. The life-span and circulation dynamics of the immunologically committed lymphocyte. J Exp Med. 1971 Feb 1;133(2):389–399. doi: 10.1084/jem.133.2.389. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Nickol A. D., Bonventre P. F. Anomalous high native resistance to athymic mice to bacterial pathogens. Infect Immun. 1977 Dec;18(3):636–645. doi: 10.1128/iai.18.3.636-645.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Shevach E. M., Rosenthal A. S. Function of macrophages in antigen recognition by guinea pig T lymphocytes. II. Role of the macrophage in the regulation of genetic control of the immune response. J Exp Med. 1973 Nov 1;138(5):1213–1229. doi: 10.1084/jem.138.5.1213. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Thomas D. W., Yamashita U., Shevach E. M. The role of Ia antigens in T cell activation. Immunol Rev. 1977;35:95–120. doi: 10.1111/j.1600-065x.1977.tb00237.x. [DOI] [PubMed] [Google Scholar]
  22. Woan M. C., Forsum U. K., McGregor D. D. Stimulation of activated rat T cells in vitro by Listeria monocytogenes antigens. Infect Immun. 1980 Sep;29(3):1102–1110. doi: 10.1128/iai.29.3.1102-1110.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Woan M. C., McGregor D. D., Forsum U. T cell-mediated cytotoxicity induced by Listeria monocytogenes. II. Specificity of cytolytic effector cells. J Immunol. 1981 Dec;127(6):2325–2330. [PubMed] [Google Scholar]
  24. Woan M. C., McGregor D. D., Goldschneider I. T cell-mediated cytotoxicity induced by Listeria monocytogenes. III. Phenotypic characteristics of mediator T cells. J Immunol. 1981 Dec;127(6):2330–2334. [PubMed] [Google Scholar]
  25. Woan M. C., McGregor D. D. T cell-mediated cytotoxicity induced by Listeria monocytogenes. I. Activation of Listeria antigen-responsive T cells. J Immunol. 1981 Dec;127(6):2319–2324. [PubMed] [Google Scholar]
  26. Zinkernagel R. M., Althage A., Adler B., Blanden R. V., Davidson W. F., Kees U., Dunlop M. B., Shreffler D. C. H-2 restriction of cell-mediated immunity to an intracellular bacterium: effector T cells are specific for Listeria antigen in association with H-21 region-coded self-markers. J Exp Med. 1977 May 1;145(5):1353–1367. doi: 10.1084/jem.145.5.1353. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Zinkernagel R. M., Blanden R. V. Macrophage activation in mice lacking thymus-derived (T) cells. Experientia. 1975 May 15;31(5):591–593. doi: 10.1007/BF01932477. [DOI] [PubMed] [Google Scholar]
  28. Zinkernagel R. M. Restriction by H-2 gene complex of transfer of cell-mediated immunity to Listeria monocytogenes. Nature. 1974 Sep 20;251(5472):230–233. doi: 10.1038/251230a0. [DOI] [PubMed] [Google Scholar]

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