Host responses within solid tumors: Non‐thymus‐derived specific cytotoxic cells within a murine mammary adenocarcinoma
The nature of host‐derived, specifically cytotoxic cells infiltrating solid murine mammary adenocarcinomas (line T1699) was investigated. Cell suspensions obtained from enzymatically dispersed tumors were separated by sedimentation velocity. The host cell fraction was heterogeneous and contained T‐l...
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Veröffentlicht in: | International journal of cancer 1975-11, Vol.16 (5), p.798-809 |
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description | The nature of host‐derived, specifically cytotoxic cells infiltrating solid murine mammary adenocarcinomas (line T1699) was investigated. Cell suspensions obtained from enzymatically dispersed tumors were separated by sedimentation velocity. The host cell fraction was heterogeneous and contained T‐lymphocytes, non‐phagocytic cells bearing Fc receptors, eosinophils and monocytes. Host cells equivalent in size to small lymphocytes and bearing Fc receptors were found to be the predominant cell type responsible for colony inhibition. These colony‐inhibiting cells were insensitive to lysis with either anti‐θ or anti‐IgG serum and complement; and they were specific both in their induction and in their mediation of cytotoxicity. Host cells made up the predominant population in spontaneously regressive tumors but only a minor component in progressive tumors, and they were totally absent from progressive tumors in X‐irradiated animals. |
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Stephen ; Yamamura, Y. ; Radov, L.</creator><creatorcontrib>Haskill, J. Stephen ; Yamamura, Y. ; Radov, L.</creatorcontrib><description>The nature of host‐derived, specifically cytotoxic cells infiltrating solid murine mammary adenocarcinomas (line T1699) was investigated. Cell suspensions obtained from enzymatically dispersed tumors were separated by sedimentation velocity. The host cell fraction was heterogeneous and contained T‐lymphocytes, non‐phagocytic cells bearing Fc receptors, eosinophils and monocytes. Host cells equivalent in size to small lymphocytes and bearing Fc receptors were found to be the predominant cell type responsible for colony inhibition. These colony‐inhibiting cells were insensitive to lysis with either anti‐θ or anti‐IgG serum and complement; and they were specific both in their induction and in their mediation of cytotoxicity. Host cells made up the predominant population in spontaneously regressive tumors but only a minor component in progressive tumors, and they were totally absent from progressive tumors in X‐irradiated animals.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.2910160512</identifier><identifier>PMID: 1081078</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adenocarcinoma - immunology ; Animals ; Antigen-Antibody Reactions - drug effects ; Cell Line ; Cell Transformation, Neoplastic - drug effects ; Cytotoxicity Tests, Immunologic ; Female ; Immunity, Cellular ; Mammary Neoplasms, Experimental - immunology ; Mice ; Mice, Inbred DBA ; Stimulation, Chemical ; T-Lymphocytes - immunology ; Trypsin - pharmacology</subject><ispartof>International journal of cancer, 1975-11, Vol.16 (5), p.798-809</ispartof><rights>Copyright © 1975 Wiley‐Liss, Inc., A Wiley Company</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2552-37c1958922ae435386615daaf570a84bbeb867cbe73c061ef06974a35f3677e13</citedby><cites>FETCH-LOGICAL-c2552-37c1958922ae435386615daaf570a84bbeb867cbe73c061ef06974a35f3677e13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.2910160512$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.2910160512$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27911,27912,45561,45562</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1081078$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Haskill, J. Stephen</creatorcontrib><creatorcontrib>Yamamura, Y.</creatorcontrib><creatorcontrib>Radov, L.</creatorcontrib><title>Host responses within solid tumors: Non‐thymus‐derived specific cytotoxic cells within a murine mammary adenocarcinoma</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>The nature of host‐derived, specifically cytotoxic cells infiltrating solid murine mammary adenocarcinomas (line T1699) was investigated. Cell suspensions obtained from enzymatically dispersed tumors were separated by sedimentation velocity. The host cell fraction was heterogeneous and contained T‐lymphocytes, non‐phagocytic cells bearing Fc receptors, eosinophils and monocytes. Host cells equivalent in size to small lymphocytes and bearing Fc receptors were found to be the predominant cell type responsible for colony inhibition. These colony‐inhibiting cells were insensitive to lysis with either anti‐θ or anti‐IgG serum and complement; and they were specific both in their induction and in their mediation of cytotoxicity. Host cells made up the predominant population in spontaneously regressive tumors but only a minor component in progressive tumors, and they were totally absent from progressive tumors in X‐irradiated animals.</description><subject>Adenocarcinoma - immunology</subject><subject>Animals</subject><subject>Antigen-Antibody Reactions - drug effects</subject><subject>Cell Line</subject><subject>Cell Transformation, Neoplastic - drug effects</subject><subject>Cytotoxicity Tests, Immunologic</subject><subject>Female</subject><subject>Immunity, Cellular</subject><subject>Mammary Neoplasms, Experimental - immunology</subject><subject>Mice</subject><subject>Mice, Inbred DBA</subject><subject>Stimulation, Chemical</subject><subject>T-Lymphocytes - immunology</subject><subject>Trypsin - pharmacology</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1975</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMFOwzAQRC0EKqVw5YbkH0jZTeo44YYqoEUVXOAcOc5GdZXElZ1SyolP4Bv5ElKKoDdOO9LMPK2GsXOEIQKEl2ahh2GKgDEIDA9YHyGVAYQoDlm_C0AgMYqP2Yn3CwBEAaMe6yEkCDLps7eJ9S135Je28eT52rRz03BvK1PwdlVb56_4g20-3z_a-aZe-U4U5MwLFdwvSZvSaK43rW3t61ZRVf1CFK9XzjTEa1XXym24KqixWjltGlurU3ZUqsrT2c8dsOfbm6fxJJg93k3H17NAh0KEQSQ1piJJw1DRKBJREscoCqVKIUElozynPImlzklGGmKkEuJUjlQkyiiWkjAasOGOq5313lGZLZ3Z_pMhZNsNs27D7G_DrnCxKyxXeU3FXvx7tM5Pd_7aVLT5h5ZN78d77C92zoHG</recordid><startdate>19751115</startdate><enddate>19751115</enddate><creator>Haskill, J. Stephen</creator><creator>Yamamura, Y.</creator><creator>Radov, L.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19751115</creationdate><title>Host responses within solid tumors: Non‐thymus‐derived specific cytotoxic cells within a murine mammary adenocarcinoma</title><author>Haskill, J. Stephen ; Yamamura, Y. ; Radov, L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2552-37c1958922ae435386615daaf570a84bbeb867cbe73c061ef06974a35f3677e13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1975</creationdate><topic>Adenocarcinoma - immunology</topic><topic>Animals</topic><topic>Antigen-Antibody Reactions - drug effects</topic><topic>Cell Line</topic><topic>Cell Transformation, Neoplastic - drug effects</topic><topic>Cytotoxicity Tests, Immunologic</topic><topic>Female</topic><topic>Immunity, Cellular</topic><topic>Mammary Neoplasms, Experimental - immunology</topic><topic>Mice</topic><topic>Mice, Inbred DBA</topic><topic>Stimulation, Chemical</topic><topic>T-Lymphocytes - immunology</topic><topic>Trypsin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haskill, J. Stephen</creatorcontrib><creatorcontrib>Yamamura, Y.</creatorcontrib><creatorcontrib>Radov, L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Haskill, J. Stephen</au><au>Yamamura, Y.</au><au>Radov, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Host responses within solid tumors: Non‐thymus‐derived specific cytotoxic cells within a murine mammary adenocarcinoma</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>1975-11-15</date><risdate>1975</risdate><volume>16</volume><issue>5</issue><spage>798</spage><epage>809</epage><pages>798-809</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><abstract>The nature of host‐derived, specifically cytotoxic cells infiltrating solid murine mammary adenocarcinomas (line T1699) was investigated. Cell suspensions obtained from enzymatically dispersed tumors were separated by sedimentation velocity. The host cell fraction was heterogeneous and contained T‐lymphocytes, non‐phagocytic cells bearing Fc receptors, eosinophils and monocytes. Host cells equivalent in size to small lymphocytes and bearing Fc receptors were found to be the predominant cell type responsible for colony inhibition. These colony‐inhibiting cells were insensitive to lysis with either anti‐θ or anti‐IgG serum and complement; and they were specific both in their induction and in their mediation of cytotoxicity. Host cells made up the predominant population in spontaneously regressive tumors but only a minor component in progressive tumors, and they were totally absent from progressive tumors in X‐irradiated animals.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>1081078</pmid><doi>10.1002/ijc.2910160512</doi><tpages>12</tpages></addata></record> |
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subjects | Adenocarcinoma - immunology Animals Antigen-Antibody Reactions - drug effects Cell Line Cell Transformation, Neoplastic - drug effects Cytotoxicity Tests, Immunologic Female Immunity, Cellular Mammary Neoplasms, Experimental - immunology Mice Mice, Inbred DBA Stimulation, Chemical T-Lymphocytes - immunology Trypsin - pharmacology |
title | Host responses within solid tumors: Non‐thymus‐derived specific cytotoxic cells within a murine mammary adenocarcinoma |
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