Cytostatic and cytotoxic activity of lymphokine-activated killer cell supernatants
Incubation of peripheral blood mononuclear cells with interleukin-2 (IL-2) results in the release of a factor which is cytostatic and cytotoxic both to tumor cell lines (A375M, A375P, C480, MCF-7, Hey) and fresh tumor cells (in the human tumor cloning assay), including breast cancer, colon cancer, m...
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Veröffentlicht in: | Cancer Immunology Immunotherapy 1989, Vol.30 (1), p.65-70 |
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creator | HERSH, E. M SCUDERI, P GRIMES, W. J CHONG, A BRAILEY, J. L GSCHWIND, C. R SALMON, S. E |
description | Incubation of peripheral blood mononuclear cells with interleukin-2 (IL-2) results in the release of a factor which is cytostatic and cytotoxic both to tumor cell lines (A375M, A375P, C480, MCF-7, Hey) and fresh tumor cells (in the human tumor cloning assay), including breast cancer, colon cancer, melanoma, myeloma and ovarian cancer. The factor cannot be detected in a 4-h chromium-release assay, but is best demonstrated after tumor cells have been to it for exposed 3 days. The factor is not cytotoxic to normal peripheral blood leukocytes or normal fibroblasts, and is not toxic to certain targets sensitive to lymphokine-activated killer (LAK) cells, such as K562 and Daudi cells. The factor is diffusible, non-dialyzable, relatively stable to heat and acid and does not contain appreciable amounts of targets resistant to interferon-alpha and beta, tumor necrosis factor beta and interleukin-1. The data suggest that there are several mechanisms of LAK cell activity against tumor cells including one which requires direct interaction of LAK and tumor cells and one which is mediated by LAK cell supernatant. The former is detected by 4-h chromium release while the latter is not. |
doi_str_mv | 10.1007/BF01665032 |
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The factor is diffusible, non-dialyzable, relatively stable to heat and acid and does not contain appreciable amounts of targets resistant to interferon-alpha and beta, tumor necrosis factor beta and interleukin-1. The data suggest that there are several mechanisms of LAK cell activity against tumor cells including one which requires direct interaction of LAK and tumor cells and one which is mediated by LAK cell supernatant. 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M</creatorcontrib><creatorcontrib>SCUDERI, P</creatorcontrib><creatorcontrib>GRIMES, W. J</creatorcontrib><creatorcontrib>CHONG, A</creatorcontrib><creatorcontrib>BRAILEY, J. L</creatorcontrib><creatorcontrib>GSCHWIND, C. R</creatorcontrib><creatorcontrib>SALMON, S. E</creatorcontrib><title>Cytostatic and cytotoxic activity of lymphokine-activated killer cell supernatants</title><title>Cancer Immunology Immunotherapy</title><addtitle>Cancer Immunol Immunother</addtitle><description>Incubation of peripheral blood mononuclear cells with interleukin-2 (IL-2) results in the release of a factor which is cytostatic and cytotoxic both to tumor cell lines (A375M, A375P, C480, MCF-7, Hey) and fresh tumor cells (in the human tumor cloning assay), including breast cancer, colon cancer, melanoma, myeloma and ovarian cancer. The factor cannot be detected in a 4-h chromium-release assay, but is best demonstrated after tumor cells have been to it for exposed 3 days. The factor is not cytotoxic to normal peripheral blood leukocytes or normal fibroblasts, and is not toxic to certain targets sensitive to lymphokine-activated killer (LAK) cells, such as K562 and Daudi cells. The factor is diffusible, non-dialyzable, relatively stable to heat and acid and does not contain appreciable amounts of targets resistant to interferon-alpha and beta, tumor necrosis factor beta and interleukin-1. The data suggest that there are several mechanisms of LAK cell activity against tumor cells including one which requires direct interaction of LAK and tumor cells and one which is mediated by LAK cell supernatant. The former is detected by 4-h chromium release while the latter is not.</description><subject>Cytotoxicity, Immunologic</subject><subject>Humans</subject><subject>Interferons - pharmacology</subject><subject>Interleukin-2 - pharmacology</subject><subject>Killer Cells, Lymphokine-Activated - immunology</subject><subject>Original</subject><subject>Tumor Cells, Cultured</subject><subject>Tumor Necrosis Factor-alpha - pharmacology</subject><issn>0340-7004</issn><issn>1432-0851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUE1Lw0AUXESptXrxLuTgSYi-_czmJFqsCgVB9BxeNxu7Nk1CdlvMvze1perpvXkzbwaGkHMK1xQgubmfAFVKAmcHZEgFZzFoSQ_JELiAOAEQx-TE-89-YZCmAzJgQoMWfEhex12ofcDgTIRVHpkehvprg0xwaxe6qC6isls283rhKhv_nDHYPFq4srRtZGxZRn7V2LbCgFXwp-SowNLbs90ckffJw9v4KZ6-PD6P76axYZqFODGAlieouSikQoTc0IIpimkuGWiV5ppzLYSSSTJDKVNGac60ktxwbgvJR-R269usZkubG1uFFsusad0S2y6r0WX_mcrNs496nVEKXCdK9A5XWwfT1t63ttg_U8g2zWa_zfbii79xe-muyp6_3PHoDZZFi5Vxfi9TCoRWlH8D31qBeA</recordid><startdate>1989</startdate><enddate>1989</enddate><creator>HERSH, E. 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E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c282t-7c0ae37a834f56aa0dc1f261a9d520869d8338446577ba559211d28653c33ef53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Cytotoxicity, Immunologic</topic><topic>Humans</topic><topic>Interferons - pharmacology</topic><topic>Interleukin-2 - pharmacology</topic><topic>Killer Cells, Lymphokine-Activated - immunology</topic><topic>Original</topic><topic>Tumor Cells, Cultured</topic><topic>Tumor Necrosis Factor-alpha - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HERSH, E. M</creatorcontrib><creatorcontrib>SCUDERI, P</creatorcontrib><creatorcontrib>GRIMES, W. J</creatorcontrib><creatorcontrib>CHONG, A</creatorcontrib><creatorcontrib>BRAILEY, J. L</creatorcontrib><creatorcontrib>GSCHWIND, C. R</creatorcontrib><creatorcontrib>SALMON, S. E</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer Immunology Immunotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HERSH, E. M</au><au>SCUDERI, P</au><au>GRIMES, W. J</au><au>CHONG, A</au><au>BRAILEY, J. L</au><au>GSCHWIND, C. R</au><au>SALMON, S. E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytostatic and cytotoxic activity of lymphokine-activated killer cell supernatants</atitle><jtitle>Cancer Immunology Immunotherapy</jtitle><addtitle>Cancer Immunol Immunother</addtitle><date>1989</date><risdate>1989</risdate><volume>30</volume><issue>1</issue><spage>65</spage><epage>70</epage><pages>65-70</pages><issn>0340-7004</issn><eissn>1432-0851</eissn><coden>CIIMDN</coden><abstract>Incubation of peripheral blood mononuclear cells with interleukin-2 (IL-2) results in the release of a factor which is cytostatic and cytotoxic both to tumor cell lines (A375M, A375P, C480, MCF-7, Hey) and fresh tumor cells (in the human tumor cloning assay), including breast cancer, colon cancer, melanoma, myeloma and ovarian cancer. The factor cannot be detected in a 4-h chromium-release assay, but is best demonstrated after tumor cells have been to it for exposed 3 days. The factor is not cytotoxic to normal peripheral blood leukocytes or normal fibroblasts, and is not toxic to certain targets sensitive to lymphokine-activated killer (LAK) cells, such as K562 and Daudi cells. The factor is diffusible, non-dialyzable, relatively stable to heat and acid and does not contain appreciable amounts of targets resistant to interferon-alpha and beta, tumor necrosis factor beta and interleukin-1. The data suggest that there are several mechanisms of LAK cell activity against tumor cells including one which requires direct interaction of LAK and tumor cells and one which is mediated by LAK cell supernatant. The former is detected by 4-h chromium release while the latter is not.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>2480843</pmid><doi>10.1007/BF01665032</doi><tpages>6</tpages></addata></record> |
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subjects | Cytotoxicity, Immunologic Humans Interferons - pharmacology Interleukin-2 - pharmacology Killer Cells, Lymphokine-Activated - immunology Original Tumor Cells, Cultured Tumor Necrosis Factor-alpha - pharmacology |
title | Cytostatic and cytotoxic activity of lymphokine-activated killer cell supernatants |
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