Abstract
The natural cytotoxic activity of lymphoid cell populations from control and BCG-stimulated rats was examined using four target cell lines, K562, CCRF/CEM, Bri8 and Mc40. In control rats, the cytotoxicity of peritoneal cells was below that of spleen cells but above that of peripheral lymph node cells. Intraperitoneal injection of BCG induced a significant dose and time-dependent augmentation of cytotoxicity by peritoneal cells from W/Not and PVG/c rats, against all four cell lines. The increased activity reached a peak on days 4 and 5 after injection and returned to control levels by day 12. Spleen and lymph node cells from stimulated rats did not show increased cytotoxicity. K562 and CCRF/CEM target cells were considerably more susceptible to killing than Bri8 and Mc40 target cells. Separation of peritoneal cells from BCG-treated rats by density-gradient centrifugation gave an interface population, enriched with mononuclear cells showing high cytotoxic activity and a pellet population enriched with polymorphs showing very low activity. Nylon-fibre column filtration gave non-adherent and adherent cytotoxic populations. Cytotoxic activity was not diminished by removing cells adhering to Sephadex G10 or cells phagocytosing carbonyl iron, suggesting that much of the activity in this system was due to non-phagocytic mononuclear cell populations.
Full text
PDF







Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Andersson L. C., Nilsson K., Gahmberg C. G. K562--a human erythroleukemic cell line. Int J Cancer. 1979 Feb;23(2):143–147. doi: 10.1002/ijc.2910230202. [DOI] [PubMed] [Google Scholar]
- Herberman R. B., Holden H. T. Natural cell-mediated immunity. Adv Cancer Res. 1978;27:305–377. doi: 10.1016/s0065-230x(08)60936-7. [DOI] [PubMed] [Google Scholar]
- Herberman R. B., Nunn M. E., Holden H. T., Lavrin D. H. Natural cytotoxic reactivity of mouse lymphoid cells against syngeneic and allogeneic tumors. II. Characterization of effector cells. Int J Cancer. 1975 Aug 15;16(2):230–239. doi: 10.1002/ijc.2910160205. [DOI] [PubMed] [Google Scholar]
- Jondal M., Pross H. Surface markers on human b and t lymphocytes. VI. Cytotoxicity against cell lines as a functional marker for lymphocyte subpopulations. Int J Cancer. 1975 Apr 15;15(4):596–605. doi: 10.1002/ijc.2910150409. [DOI] [PubMed] [Google Scholar]
- Kiessling R., Haller O. Natural killer cells in the mouse: an alternative immune surveillance mechanism? Contemp Top Immunobiol. 1978;8:171–201. doi: 10.1007/978-1-4684-0922-2_6. [DOI] [PubMed] [Google Scholar]
- Kiessling R., Klein E., Pross H., Wigzell H. "Natural" killer cells in the mouse. II. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Characteristics of the killer cell. Eur J Immunol. 1975 Feb;5(2):117–121. doi: 10.1002/eji.1830050209. [DOI] [PubMed] [Google Scholar]
- Kiuchi M., Takasugi M. The nonselective cytotoxic cell (N cell). J Natl Cancer Inst. 1976 Mar;56(3):575–582. doi: 10.1093/jnci/56.3.575. [DOI] [PubMed] [Google Scholar]
- Ly I. A., Mishell R. I. Separation of mouse spleen cells by passage through columns of sephadex G-10. J Immunol Methods. 1974 Aug;5(3):239–247. doi: 10.1016/0022-1759(74)90108-2. [DOI] [PubMed] [Google Scholar]
- Oehler J. R., Lindsay L. R., Nunn M. E., Holden H. T., Herberman R. B. Natural cell-mediated cytotoxicity in rats. II. In vivo augmentation of NK-cell activity. Int J Cancer. 1978 Feb 15;21(2):210–220. doi: 10.1002/ijc.2910210213. [DOI] [PubMed] [Google Scholar]
- Ojo E., Haller O., Wigzell H. Corynebacterium parvum-induced peritoneal exudate cells with rapid cytolytic activity against tumour cells are non-phagocytic cells with characteristics of natural killer cells. Scand J Immunol. 1978;8(3):215–222. doi: 10.1111/j.1365-3083.1978.tb00513.x. [DOI] [PubMed] [Google Scholar]
- Potter M. R., Moore M. Organ distribution of natural cytotoxicity in the rat. Clin Exp Immunol. 1978 Oct;34(1):78–86. [PMC free article] [PubMed] [Google Scholar]
- Potter M. R., Moore M. PHA stimulation of separated human lymphocyte populations. Clin Exp Immunol. 1975 Sep;21(3):456–467. [PMC free article] [PubMed] [Google Scholar]
- Potter M. R., Moore M. The effect of adherent and phagocytic cells on human lymphocyte PHA responsiveness. Clin Exp Immunol. 1977 Jan;27(1):159–164. [PMC free article] [PubMed] [Google Scholar]
- Pross H. F., Baines M. G. Spontaneous human lymphocyte-mediated cytotoxicity againts tumour target cells. I. The effect of malignant disease. Int J Cancer. 1976 Nov 15;18(5):593–604. doi: 10.1002/ijc.2910180508. [DOI] [PubMed] [Google Scholar]
- Pross H. F., Jondal M. Cytotoxic lymphocytes from normal donors. A functional marker of human non-T lymphocytes. Clin Exp Immunol. 1975 Aug;21(2):226–235. [PMC free article] [PubMed] [Google Scholar]
- Shellam G. R. Gross-virus-induced lymphoma in the rat. V. Natural cytotoxic cells are non-T cells. Int J Cancer. 1977 Feb 15;19(2):225–235. doi: 10.1002/ijc.2910190212. [DOI] [PubMed] [Google Scholar]
- Tracey D. E., Wolfe S. A., Durdik J. M., Henney C. S. BCG-induced murine effector cells. I. Cytolytic activity in peritoneal exudates: an early response to BCG. J Immunol. 1977 Sep;119(3):1145–1151. [PubMed] [Google Scholar]
- Wolfe S. A., Tracey D. E., Henney C. S. BCG-induced murine effector cells. II. Characterization of natural killer cells in peritoneal exudates. J Immunol. 1977 Sep;119(3):1152–1158. [PubMed] [Google Scholar]
- Wolfe S. A., Tracey D. E., Henney C. S. Introduction of "natural" killer' cells by BCG. Nature. 1976 Aug 12;262(5569):584–586. doi: 10.1038/262584a0. [DOI] [PubMed] [Google Scholar]
