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. 1984 Apr;51(4):703–710.

T cell proliferation in Mycobacterium lepraemurium infection. II. Characterization of cells that transfer resistance in subcutaneously infected mice.

R C Mathew, J Curtis, J L Turk
PMCID: PMC1454559  PMID: 6368373

Abstract

T lymphocyte proliferation, Lyt phenotypes and their role in the evolution of protective immunity were studied in BALB/c and C57BL/6 mice infected subcutaneously with Mycobacterium lepraemurium. Antigen-induced proliferation was not demonstrable with T-enriched cells obtained from the spleens. However, these cells were capable of spontaneously proliferating in the absence of added antigen for a limited period. This proliferation was dependent on the presence of a phagocytic and adherent accessory cell. During the period when the T cells proliferated spontaneously they consisted of a mixture of Lyt-1 and Lyt-23 and were able to transfer protection to syngeneic recipient mice. Furthermore, the multiplication of the organisms was curbed during the same period demonstrating a strong association between the ability to proliferate spontaneously Lyt-1/Lyt-23 cells and protective immunity. T cells from normal BALB/c mice showed a marked suppressive effect on protection suggesting that these cells may be responsible for the susceptibility of this strain to a moderate subcutaneous infection.

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Selected References

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

  1. Alexander J. Adoptive transfer of immunity and suppression by cells and serum in early Mycobacterium lepraemurium infections of mice. Parasite Immunol. 1979 Summer;1(2):159–166. doi: 10.1111/j.1365-3024.1979.tb00703.x. [DOI] [PubMed] [Google Scholar]
  2. Curtis J., Turk J. L. Mitsuda-type lepromin reactions as a measure of host resistance in Mycobacterium lepraemurium infection. Infect Immun. 1979 May;24(2):492–500. doi: 10.1128/iai.24.2.492-500.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. HART P. D., REES R. J. Effect of macrocyclon in acute and chronic pulmonary tuberculous infection in mice as shown by viable and total bacterial counts. Br J Exp Pathol. 1960 Aug;41:414–421. [PMC free article] [PubMed] [Google Scholar]
  4. Hertel-Wulff B. An in vitro assay for the quantitation of phagocytic cells of different anatomic origin. Acta Pathol Microbiol Scand C. 1977 Aug;85C(4):253–259. doi: 10.1111/j.1699-0463.1977.tb03639.x. [DOI] [PubMed] [Google Scholar]
  5. 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]
  6. Lefford M. J. Transfer of adoptive immunity to tuberculosis in mice. Infect Immun. 1975 Jun;11(6):1174–1181. doi: 10.1128/iai.11.6.1174-1181.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Liew F. Y., Hale C., Howard J. G. Immunologic regulation of experimental cutaneous leishmaniasis. V. Characterization of effector and specific suppressor T cells. J Immunol. 1982 Apr;128(4):1917–1922. [PubMed] [Google Scholar]
  8. Mathew R. C., Curtis J., Turk J. L. T cell proliferation in Mycobacterium lepraemurium infection. I. Lack of correlation between antigen-specific proliferation of Lyt 1 + 23- cells and resistance in lethal infections. Immunology. 1984 Jan;51(1):185–192. [PMC free article] [PubMed] [Google Scholar]
  9. Patel P. J. Antibacterial resistance in mice infected with Mycobacterium lepraemurium. Clin Exp Immunol. 1981 Sep;45(3):654–661. [PMC free article] [PubMed] [Google Scholar]
  10. Patel P. J., Lefford M. J. Antigen specific lymphocyte transformation, delayed hypersensitivity and protective immunity. I. Kinetics of the response. Cell Immunol. 1978 May;37(2):315–326. doi: 10.1016/0008-8749(78)90200-9. [DOI] [PubMed] [Google Scholar]
  11. Pavlov H., Hogarth M., McKenzie I. F., Cheers C. In vivo and in vitro effects of monoclonal antibody to Ly antigens on immunity to infection. Cell Immunol. 1982 Jul 15;71(1):127–138. doi: 10.1016/0008-8749(82)90502-0. [DOI] [PubMed] [Google Scholar]
  12. Rook G. A. The immunological consequences of antigen overload in experimental mycobacterial infections of mice. Clin Exp Immunol. 1975 Jan;19(1):167–177. [PMC free article] [PubMed] [Google Scholar]
  13. Rook G. A. The potentiating, mitogenic and inhibitory effects on lymphocytes in vitro, of macrophages in the lymph nodes of mice 'overloaded' with mycobacterial products. Clin Exp Immunol. 1975 Jul;21(1):163–172. [PMC free article] [PubMed] [Google Scholar]
  14. Schwartz R. H., Yano A., Paul W. E. Interaction between antigen-presenting cells and primed T lymphocytes: an assessment of Ir gene expression in the antigen-presenting cell. Immunol Rev. 1978;40:153–180. doi: 10.1111/j.1600-065x.1978.tb00405.x. [DOI] [PubMed] [Google Scholar]

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