Cancer Research AACR Conference on Molecular Diagnostics - 2008  Tumor Immunology: New Perspectives
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[Cancer Research 48, 891-898, February 15, 1988]
© 1988 American Association for Cancer Research

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Distinction of Partially Purified Human Natural Killer Cytotoxic Factor from Recombinant Human Tumor Necrosis Factor and Recombinant Human Lymphotoxin1

Tammo Bialas2, Jonathan Kolitz, Ester Levi, Andrej Polivka, Sadik Oez, Glenn Miller and Karl Welte

Laboratory of Cytokine Biology, Memorial Sloan-Kettering Cancer Center, New York, New York 10021

Natural killer cell cytotoxic factor (NKCF), a cytotoxic factor contributing to human natural killer cell-mediated cytotoxicity, was generated from lymphocyte-conditioned medium using various stimuli. Crude NKCF activity was concentrated, and partially purified by ammonium sulfate precipitation and gel filtration. NKCF activities eluted as two molecular weight peaks, corresponding to Mr 33,000–43,000 (pool I) and approximately Mr 5,000 (pool II). The cytotoxic activity and target specificity of the partially purified NKCFs were found to be different from both recombinant human TNF and recombinant human lymphotoxin. In the NKCF assay, up to 106 units/ml of TNF and lymphotoxin had virtually no effect, whereas both NKCFs lysed 22% (range 17–33%) of the NK-sensitive target K562. In contrast, TNF and lymphotoxin were active in a standard assay against the sensitive murine L929 fibroblast cell line in all concentrations tested (10-1–106 units/ml). In addition, the effect of these cytotoxic factors in a short-term (4-h) chromium-release assay using peripheral blood mononuclear cells as effector cells was tested: only NKCF (pool I), but not TNF, lymphotoxin, or low molecular weight NKCF (pool II), enhanced NK and lymphokine-activated killer cell cytolysis, both against the NK-sensitive target K562 and the NK-resistant melanoma cell line SK-MEL 30. Results were not affected in the presence of neutralizing antibodies against TNF. NKCF could, therefore, be distinguished from TNF and lymphotoxin with respect to their biological activities.

1 This work was supported in part by Grants CA 23766 and CA 33484 from the National Institutes of Health and Grant Bi 317/1-1 from the Deutsche Forschungsgemeinschaft.

2 To whom requests for reprints should be addressed, at Laboratory of Cytokine Biology, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021.

Received 3/23/87. Revised 7/27/87. Revised 11/11/87. Accepted 11/16/87.







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Copyright © 1988 by the American Association for Cancer Research.