Mediation of mouse natural cytotoxic activity by tumour necrosis factor (original) (raw)
- Letter
- Published: 12 June 1986
- Llewellyn H. Mason1,
- Bonnie J. Mathieson1,
- Shu-Mei Liang1 na1,
- David A. Flick1 na2 &
- …
- Ronald B. Herberman1
Nature volume 321, pages 700–702 (1986)Cite this article
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Abstract
Natural cell-mediated cytotoxic activity in the mouse has been associated with two types of effector cells, the natural killer (NK) cell and the natural cytotoxic (NC) cell, which seem to differ with regard to their patterns of target selectivity, cell surface characteristics and susceptibility to regulatory factors1. During studies on the mechanism of action of cytotoxic molecules, it became evident that WEHI-164, the prototype NC target cell, was highly susceptible to direct lysis by both human and mouse recombinant tumour necrosis factor (TNF). Here we show that NC, but not NK activity mediated by normal splenocytes, is abrogated by rabbit antibodies to recombinant and natural TNF, respectively. Thus, the cell-mediated activity defined as NC is due to release of TNF by normal spleen cells and does not represent a unique natural effector mechanism.
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Author notes
- Shu-Mei Liang: Biogen SA, PO Box 121, Geneva 24, Switzerland
- David A. Flick: Department of Immunology and Medical Microbiology, University of Florida College of Medicine, Gainesville, Florida 32610, USA
Authors and Affiliations
- Biological Therapeutics Branch, Biological Response Modifiers Program, Division of Cancer Treatment, National Cancer Institute, National Institutes of Health, Frederick Cancer Research Facility, Building 560, Room 31-93A, Frederick, Maryland, 21701, USA
John R. Ortaldo, Llewellyn H. Mason, Bonnie J. Mathieson, Shu-Mei Liang, David A. Flick & Ronald B. Herberman
Authors
- John R. Ortaldo
- Llewellyn H. Mason
- Bonnie J. Mathieson
- Shu-Mei Liang
- David A. Flick
- Ronald B. Herberman
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Ortaldo, J., Mason, L., Mathieson, B. et al. Mediation of mouse natural cytotoxic activity by tumour necrosis factor.Nature 321, 700–702 (1986). https://doi.org/10.1038/321700a0
- Received: 31 December 1985
- Accepted: 04 April 1986
- Issue date: 12 June 1986
- DOI: https://doi.org/10.1038/321700a0