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. 1988 Jul;64(3):457–461.

Lectin-induced cytotoxic activity in spleen cells from young and old mice. Age-related changes in types of effector cells, lymphokine production and response.

R K Saxena 1, Q B Saxena 1, W H Adler 1
PMCID: PMC1385058  PMID: 3137156

Abstract

Concanavalin A (Con A)-induced cytotoxic activity, interferon (IFN) and interleukin-2 (IL-2) levels in cultures of spleen cells from young (2-3 months) and old (22-24 months) C57BL/6 female mice were studied. Con A-activated spleen cells from old mice attained significantly higher cytotoxic activity compared with activated spleen cells from young mice. Activated spleen cells from old and young mice showed differences in their ability to lyse different types of target cells. Both could lyse P-815 cells, neither could lyse K562 cells, and only activated cells from old mice could lyse EL-4 cells. Cytotoxic spleen cells from the old mice were more sensitive to anti-asialo-GM-1 and anti-Lyt-2.2 plus complement (C) treatment. While levels of IL-2 produced by spleen cells from young mice were higher, the addition of exogenous IL-2 had no effect on cytotoxic activity of the spleen cells from old mice. Exogenous IL-2, however, could lower cytotoxic activity of Con A-activated spleen cells from young mice. Activated spleen cells from old mice generated higher levels of IFN-gamma while the addition of an anti-IFN-gamma antibody boosted the level of cytotoxicity by Con A-activated spleen cells from young mice. These results suggest that IFN-gamma may act as a feedback inhibitory signal regulating the levels of cytotoxicity induced in spleen cells from young mice in response to Con A. The cytotoxic activity generated in Con A-activated spleen cells from old mice reflects a defect in this feed-back regulation.

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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., Boyse E. A. Functional subclasses of T lymphocytes bearing different Ly antigens. II. Cooperation between subclasses of Ly+ cells in the generation of killer activity. J Exp Med. 1975 Jun 1;141(6):1390–1399. doi: 10.1084/jem.141.6.1390. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Farrar W. L., Johnson H. M., Farrar J. J. Regulation of the production of immune interferon and cytotoxic T lymphocytes by interleukin 2. J Immunol. 1981 Mar;126(3):1120–1125. [PubMed] [Google Scholar]
  3. Farrar W. L., Mizel S. B., Farrar J. J. Participation of lymphocyte activating factor (Interleukin 1) in the induction of cytotoxic T cell responses. J Immunol. 1980 Mar;124(3):1371–1377. [PubMed] [Google Scholar]
  4. Friedman R. M., Vogel S. N. Interferons with special emphasis on the immune system. Adv Immunol. 1983;34:97–140. doi: 10.1016/s0065-2776(08)60378-8. [DOI] [PubMed] [Google Scholar]
  5. Gillis S., Ferm M. M., Ou W., Smith K. A. T cell growth factor: parameters of production and a quantitative microassay for activity. J Immunol. 1978 Jun;120(6):2027–2032. [PubMed] [Google Scholar]
  6. Heine J. W., Adler W. H. The quantitative production of interferon by mitogen-stimulated mouse lymphocytes as a function of age and its effect on the lymphocytes proliferative response. J Immunol. 1977 Apr;118(4):1366–1369. [PubMed] [Google Scholar]
  7. Hirano T., Nordin A. A. Age-associated decline in the in vitro development of cytotoxic lymphocytes in NZB mice. J Immunol. 1976 Oct;117(4):1093–1098. [PubMed] [Google Scholar]
  8. Holda J. H., Maier T., Claman H. N. Natural suppressor activity in graft-vs-host spleen and normal bone marrow is augmented by IL 2 and interferon-gamma. J Immunol. 1986 Dec 1;137(11):3538–3543. [PubMed] [Google Scholar]
  9. Makinodan T., Adler W. H. Effects of aging on the differentiation and proliferation potentials of cells of the immune system. Fed Proc. 1975 Feb;34(2):153–158. [PubMed] [Google Scholar]
  10. Saxena R. K., Adler W. H. Modulation of natural cytotoxicity by alloantibodies. I. Alloantisera enhancement of cytotoxicity of mouse spleen cells toward a human myeloid cell line. J Immunol. 1979 Aug;123(2):846–851. [PubMed] [Google Scholar]
  11. Saxena R. K., Adler W. H., Nordin A. A. Modulation of natural cytotoxicity by alloantibodies. IV. A comparative study of the activation of mouse spleen cell cytotoxicity by anti H-2 antisera, interferon, and mitogens. Cell Immunol. 1981 Sep 1;63(1):28–41. doi: 10.1016/0008-8749(81)90026-5. [DOI] [PubMed] [Google Scholar]
  12. Saxena R. K., Saxena Q. B., Adler W. H. Interleukin-2-induced activation of natural killer activity in spleen cells from old and young mice. Immunology. 1984 Apr;51(4):719–726. [PMC free article] [PubMed] [Google Scholar]
  13. Stavy L., Treves A. J., Feldman M. Capacity of thymic cells to effect target cell lysis following treatment with concanavalin A. Cell Immunol. 1972 Apr;3(4):623–628. doi: 10.1016/0008-8749(72)90124-4. [DOI] [PubMed] [Google Scholar]
  14. Thoman M. L., Weigle W. O. Cell-mediated immunity in aged mice: an underlying lesion in IL 2 synthesis. J Immunol. 1982 May;128(5):2358–2361. [PubMed] [Google Scholar]
  15. Walters C. S., Claman H. N. Age-related changes in cell-mediated immunity in BALB/C mice. J Immunol. 1975 Nov;115(5):1438–1443. [PubMed] [Google Scholar]

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