Cultures of purified human natural killer cells: Growth in the presence of interleukin 2 |
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Authors: | Tuomo Timonen John R. Ortaldo Beda M. Stadler Guy D. Bonnard Susan O. Sharrow Ronald B. Herberman |
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Affiliation: | 1. Laboratory of Immunodiagnosis, National Cancer Institute, U.S.A.;2. Immunology Branch, National Cancer Institute, U.S.A.;3. Laboratory of Microbiology and Immunology, National Institute of Dental Research, National Institutes of Health, Bethesda, Maryland 20205 U.S.A. |
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Abstract: | We have isolated highly enriched populations of LGL, which are virtually devoid of mature typical lymphocytes (as enumerated by morphological and surface antigen analysis using monoclonal antibodies e.g., OKT3) in comparison to T cells which contain greater than 95% sheep erythrocyte-forming cells and are devoid of LGL and activities. Both types of cells grew in the presence of crude or partially purified IL-2. Cultures of LGL could be initiated consistently even in the absence of lectins and the cultured LGL retained their characteristic morphology and cytotoxic activity. However, within 7–10 days after initiation, the cultured LGL changed in surface phenotype to become antigenically indistinguishable from cultured T cells. |
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Keywords: | To whom all correspondence should be addressed: BRTB BRMP NCI-FCRF Frederick Md. 21701. |
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