Abstract
The ability of mononuclear cells (MC) from peripheral blood of normal cattle to lyse a variety of cells was tested in a 51Cr-release microcytotoxicity assay. Several types of bovine cells infected with parainfluenza 3 virus (PI3V) were susceptible to natural cytotoxicity. Bovine cells infected with infectious bovine rhinotracheitis virus or noncytopathogenic bovine viral diarrhea virus, uninfected bovine cells, and human cell lines MOLT-3, HSB-2, K562, and U-937 were not susceptible. The period of time that target cells need to be infected with PI3V to achieve maximal cytotoxicity was determined. Target cells were infected with PI3V and MC, added 1 h later. After the addition of effector cells, significant levels of cytotoxicity were recorded at 17 h. Maximal cytotoxicity occurred 22 to 24 h postinfection. To define the optimal time that MC must be present, cells were infected with PI3V for a total of 24 h, and MC were left in contact with target cells for various time intervals. Maximal cytotoxicity was recorded when effector cells were present for 20 h, suggesting that a period of activation was needed to stimulate effector cell function. Removal of adherent mononuclear cells on Sephadex G-10 columns did not reduce the low level of cytotoxicity against uninfected target cells, but markedly reduced the level of cytotoxicity against PI3V-infected cells. The effector cell was nonphagocytic and nonadherent. These characteristics and the fact that target cell lysis was independent of genetic restriction indicate that effector cells are similar to natural killer cells described in other species.
Full text
PDF





Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Altman A., Rapp H. J. Natural cell-mediated cytotoxicity in guinea pigs: properties and specificity of natural killer cells. J Immunol. 1978 Dec;121(6):2244–2252. [PubMed] [Google Scholar]
- Anderson M. J. Innate cytotoxicity of CBA mouse spleen cells to Sendai virus-infected L cells. Infect Immun. 1978 Jun;20(3):608–612. doi: 10.1128/iai.20.3.608-612.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Armerding D., Rossiter H. Induction of cytolytic T- and B-cell responses against influenza virus infections. Infect Immun. 1980 Jun;28(3):799–811. doi: 10.1128/iai.28.3.799-811.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bancroft G. J., Shellam G. R., Chalmer J. E. Genetic influences on the augmentation of natural killer (NK) cells during murine cytomegalovirus infection: correlation with patterns of resistance. J Immunol. 1981 Mar;126(3):988–994. [PubMed] [Google Scholar]
- Datta S. K., Gallagher M. T., Trentin J. J. Natural killer cell-mediated cytotoxicity versus lymphoma in hamsters. Prog Exp Tumor Res. 1979;23:180–193. doi: 10.1159/000401425. [DOI] [PubMed] [Google Scholar]
- Djeu J. Y., Heinbaugh J. A., Holden H. T., Herberman R. B. Augmentation of mouse natural killer cell activity by interferon and interferon inducers. J Immunol. 1979 Jan;122(1):175–181. [PubMed] [Google Scholar]
- Djeu J. Y., Heinbaugh J. A., Holden H. T., Herberman R. B. Role of macrophages in the augementation of mouse natural killer cell activity by poly I:C and interferon. J Immunol. 1979 Jan;122(1):182–188. [PubMed] [Google Scholar]
- Djeu J. Y., Huang K. Y., Herberman R. B. Augmentation of mouse natural killer activity and induction of interferon by tumor cells in vivo. J Exp Med. 1980 Apr 1;151(4):781–789. doi: 10.1084/jem.151.4.781. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Emery D. L., Eugui E. M., Nelson R. T., Tenywa T. Cell-mediated immune responses to Theileria parva (East Coast fever) during immunization and lethal infections in cattle. Immunology. 1981 Jun;43(2):323–336. [PMC free article] [PubMed] [Google Scholar]
- Gidlund M., Orn A., Wigzell H., Senik A., Gresser I. Enhanced NK cell activity in mice injected with interferon and interferon inducers. Nature. 1978 Jun 29;273(5665):759–761. doi: 10.1038/273759a0. [DOI] [PubMed] [Google Scholar]
- Hansson M., Bakacs K. K., Kiessling R., Klein G. Intra- and interspecies reactivity of human and mouse natural killer (NK) cells. J Immunol. 1978 Jul;121(1):6–12. [PubMed] [Google Scholar]
- Herberman R. B., Bartram S., Haskill J. S., Nunn M., Holden H. T., West W. H. Fc receptors on mouse effector cells mediating natural cytotoxicity against tumor cells. J Immunol. 1977 Jul;119(1):322–326. [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]
- Huddlestone J. R., Merigan T. C., Jr, Oldstone M. B. Induction and kinetics of natural killer cells in humans following interferon therapy. Nature. 1979 Nov 22;282(5737):417–419. doi: 10.1038/282417a0. [DOI] [PubMed] [Google Scholar]
- Jerrells T. R., Dean J. H., Richardson G. L., Herberman R. B. Depletion of monocytes from human peripheral blood mononuclear leukocytes: comparison of the sephadex G-10 column method with other commonly used techniques. J Immunol Methods. 1980;32(1):11–29. doi: 10.1016/0022-1759(80)90113-1. [DOI] [PubMed] [Google Scholar]
- Kohl S., Lawman M. J., Rouse B. T., Cahall D. L. Effect of herpes simplex virus infection on murine antibody-dependent cellular cytotoxicity and natural killer cytotoxicity. Infect Immun. 1981 Feb;31(2):704–711. doi: 10.1128/iai.31.2.704-711.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kohl S., Starr S. E., oleske J. M., Shore S. L., Ashman R. B., Nahmias A. J. Human monocyte-macrophage-mediated antibody-dependent cytotoxicity to herpes simplex virus-infected cells. J Immunol. 1977 Mar;118(3):729–735. [PubMed] [Google Scholar]
- Nunn M. E., Herberman R. B., Holden H. T. Natural cell-mediated cytotoxicity in mice against non-lymphoid tumor cells and some normal cells. Int J Cancer. 1977 Sep 15;20(3):381–387. doi: 10.1002/ijc.2910200309. [DOI] [PubMed] [Google Scholar]
- Oehler J. R., Lindsay L. R., Nunn M. E., Herberman R. B. Natural cell-mediated cytotoxicity in rats. I. Tissue and strain distribution, and demonstration of a membrance receptor for the Fc portion of IgG. Int J Cancer. 1978 Feb 15;21(2):204–209. doi: 10.1002/ijc.2910210212. [DOI] [PubMed] [Google Scholar]
- Paciucci P. A., Macphail S., Bach F. H., Zarling J. M. Requirements for T cells in alloantigen-induced generation of non-T cell-mediated cytotoxicity against syngeneic mouse sarcoma cells. J Immunol. 1980 Jul;125(1):36–39. [PubMed] [Google Scholar]
- Roder J. C., Karre K., Kiessling R. Natural killer cells. Prog Allergy. 1981;28:66–159. [PubMed] [Google Scholar]
- Rosenberg E. B., McCoy J. L., Green S. S., Donnelly F. C., Siwarski D. F., Levine P. H., Herberman R. B. Destruction of human lymphoid tissue-culture cell lines by human peripheral lymphocytes in 51Cr-release cellular cytotoxicity assays. J Natl Cancer Inst. 1974 Feb;52(2):345–352. doi: 10.1093/jnci/52.2.345. [DOI] [PubMed] [Google Scholar]
- Rossi C. R., Kiesel G. K. Microtiter tests for detecting antibody in bovine serum to parainfluenza 3 virus, infectious bovine rhinotracheitis virus, and bovine virus diarrhea virus. Appl Microbiol. 1971 Jul;22(1):32–36. doi: 10.1128/am.22.1.32-36.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Santoli D., Trinchieri G., Koprowski H. Cell-mediated cytotoxicity against virus-infected target cells in humans. II. Interferon induction and activation of natural killer cells. J Immunol. 1978 Aug;121(2):532–538. [PubMed] [Google Scholar]
- Santoli D., Trinchieri G., Lief F. S. Cell-mediated cytotoxicity against virus-infected target cells in humans. I. Characterization of the effector lymphocyte. J Immunol. 1978 Aug;121(2):526–531. [PubMed] [Google Scholar]
- Sharma J. M., Okazaki W. Natural killer cell activity in chickens: target cell analysis and effect of antithymocyte serum on effector cells. Infect Immun. 1981 Mar;31(3):1078–1085. doi: 10.1128/iai.31.3.1078-1085.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Silva A., Bonavida B., Targan S. Mode of action of interferon-mediated modulation of natural killer cytotoxic activity: recruitment of pre-NK cells and enhanced kinetics of lysis. J Immunol. 1980 Aug;125(2):479–484. [PubMed] [Google Scholar]
- Stott E. J., Probert M., Thomas L. H. Cytotoxicity of alveolar macrophages for virus-infected cells. Nature. 1975 Jun 26;255(5511):710–712. doi: 10.1038/255710a0. [DOI] [PubMed] [Google Scholar]
- Tracey D. E. The requirement for macrophages in the augmentation of natural killer cell activity by BCG. J Immunol. 1979 Aug;123(2):840–845. [PubMed] [Google Scholar]
- Trinchieri G., Santoli D., Dee R. R., Knowles B. B. Anti-viral activity induced by culturing lymphocytes with tumor-derived or virus-transformed cells. Identification of the anti-viral activity as interferon and characterization of the human effector lymphocyte subpopulation. J Exp Med. 1978 May 1;147(5):1299–1313. doi: 10.1084/jem.147.5.1299. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Welsh R. M., Jr, Hallenbeck L. A. Effect of virus infections on target cell susceptibility to natural killer cell-mediated lysis. J Immunol. 1980 May;124(5):2491–2497. [PubMed] [Google Scholar]
- Welsh R. M., Jr, Zinkernagel R. M., Hallenbeck L. A. Cytotoxic cells induced during lymphocytic choriomeningitis virus infection of mice. II. "Specificities" of the natural killer cells. J Immunol. 1979 Feb;122(2):475–481. [PubMed] [Google Scholar]
- de Vries J. E., Mendelsohn J., Bont W. S. The role of target cells, monocytes, and Fc receptor-bearing lymphocytes in human spontaneous cell-mediated cytotoxicity and antibody-dependent cellular cytotoxicity. J Immunol. 1980 Jul;125(1):396–405. [PubMed] [Google Scholar]
