Immunotherapy of a murine colon cancer with syngeneic spleen cells, immune RNA and tumor antigen
In combination with xenogeneic immune RNA (l-RNA) and tumor antigen (TA), syngeneic spleen cells inhibited the growth of a N-methyl-N-nitrosourethane-induced colon carcinoma (CT-26) in BALB/c mice. The sequential administration of 1 X 10(7) spleen cells, l mg of anti-CT-26 l-RNA and 0.4 mg of CT-26...
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Veröffentlicht in: | International journal of cancer 1982-01, Vol.29 (1), p.107-112 |
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description | In combination with xenogeneic immune RNA (l-RNA) and tumor antigen (TA), syngeneic spleen cells inhibited the growth of a N-methyl-N-nitrosourethane-induced colon carcinoma (CT-26) in BALB/c mice. The sequential administration of 1 X 10(7) spleen cells, l mg of anti-CT-26 l-RNA and 0.4 mg of CT-26 TA resulted in a 20% survival rate of mice bearing established CT-26 tumors. On the other hand, administration of the spleen cells only, l-RNA only or TA only was not effective in inhibiting tumor growth. Similarly, when any one of the three agents (l-RNA, TA and spleen cells) was omitted, no anti-tumor effect was obtained. A higher dose (1 X 10(8) and a lower dose(1 X 10(6) of spleen cells decreased the anti-tumor effect of this combination therapy. A higher dose (2 mg) and a lower dose (0.5 mg) of l-RNA, as well as a higher dose of TA (0.8 mg) had no influence on the anti-tumor effect. However, a lower dose of TA (0.2 mg) in combination with spleen cells and l-RNA decreased the anti-tumor effect. When all three agents were administered at higher or lower doses, no anti-tumor effect was obtained. When mice bearing CT-26 tumors were treated with spleen cells, plus l-RNA directed against a syngeneic but antigenically different tumor (BP/B/5) and BP/B/5/TA, with spleen cells plus CT 26 I-RNA and BP/B/5TA, or with spleen cells plus BP/B/5 l-RNA and CT-26 TA, no anti-tumor effect was observed. These results indicate that the anti-tumor responses observed were due to tumor-specific immune responses. In conclusion, in order to obtain growth retardation or regression of established CT-26 tumor transplants, the sequential administration of all three agents (spleen cells, l-RNA and TA) was required. The optimal doses of each agent were found to be 1 X 10(7) spleen cells, 0.5 mg or 1 mg of l-RNA and 0.4 mg of tumor antigen. Higher or lower doses decreased the anti-tumor effect. Tumor-specific immune reactions appeared to be involved. |
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The sequential administration of 1 X 10(7) spleen cells, l mg of anti-CT-26 l-RNA and 0.4 mg of CT-26 TA resulted in a 20% survival rate of mice bearing established CT-26 tumors. On the other hand, administration of the spleen cells only, l-RNA only or TA only was not effective in inhibiting tumor growth. Similarly, when any one of the three agents (l-RNA, TA and spleen cells) was omitted, no anti-tumor effect was obtained. A higher dose (1 X 10(8) and a lower dose(1 X 10(6) of spleen cells decreased the anti-tumor effect of this combination therapy. A higher dose (2 mg) and a lower dose (0.5 mg) of l-RNA, as well as a higher dose of TA (0.8 mg) had no influence on the anti-tumor effect. However, a lower dose of TA (0.2 mg) in combination with spleen cells and l-RNA decreased the anti-tumor effect. When all three agents were administered at higher or lower doses, no anti-tumor effect was obtained. When mice bearing CT-26 tumors were treated with spleen cells, plus l-RNA directed against a syngeneic but antigenically different tumor (BP/B/5) and BP/B/5/TA, with spleen cells plus CT 26 I-RNA and BP/B/5TA, or with spleen cells plus BP/B/5 l-RNA and CT-26 TA, no anti-tumor effect was observed. These results indicate that the anti-tumor responses observed were due to tumor-specific immune responses. In conclusion, in order to obtain growth retardation or regression of established CT-26 tumor transplants, the sequential administration of all three agents (spleen cells, l-RNA and TA) was required. The optimal doses of each agent were found to be 1 X 10(7) spleen cells, 0.5 mg or 1 mg of l-RNA and 0.4 mg of tumor antigen. Higher or lower doses decreased the anti-tumor effect. Tumor-specific immune reactions appeared to be involved.</description><identifier>ISSN: 0020-7136</identifier><identifier>PMID: 6174460</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Antigens, Neoplasm - immunology ; Colonic Neoplasms - chemically induced ; Colonic Neoplasms - therapy ; Dose-Response Relationship, Immunologic ; Immunotherapy - methods ; Mice ; Mice, Inbred BALB C ; Neoplasm Transplantation ; Neoplasms, Experimental - therapy ; Nitrosomethylurethane ; RNA - immunology ; Spleen - immunology</subject><ispartof>International journal of cancer, 1982-01, Vol.29 (1), p.107-112</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6174460$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fukushima, M</creatorcontrib><creatorcontrib>Colmerauer, M E</creatorcontrib><creatorcontrib>Nayak, S K</creatorcontrib><creatorcontrib>Koziol, J A</creatorcontrib><creatorcontrib>Pilch, Y H</creatorcontrib><title>Immunotherapy of a murine colon cancer with syngeneic spleen cells, immune RNA and tumor antigen</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>In combination with xenogeneic immune RNA (l-RNA) and tumor antigen (TA), syngeneic spleen cells inhibited the growth of a N-methyl-N-nitrosourethane-induced colon carcinoma (CT-26) in BALB/c mice. The sequential administration of 1 X 10(7) spleen cells, l mg of anti-CT-26 l-RNA and 0.4 mg of CT-26 TA resulted in a 20% survival rate of mice bearing established CT-26 tumors. On the other hand, administration of the spleen cells only, l-RNA only or TA only was not effective in inhibiting tumor growth. Similarly, when any one of the three agents (l-RNA, TA and spleen cells) was omitted, no anti-tumor effect was obtained. A higher dose (1 X 10(8) and a lower dose(1 X 10(6) of spleen cells decreased the anti-tumor effect of this combination therapy. A higher dose (2 mg) and a lower dose (0.5 mg) of l-RNA, as well as a higher dose of TA (0.8 mg) had no influence on the anti-tumor effect. However, a lower dose of TA (0.2 mg) in combination with spleen cells and l-RNA decreased the anti-tumor effect. When all three agents were administered at higher or lower doses, no anti-tumor effect was obtained. When mice bearing CT-26 tumors were treated with spleen cells, plus l-RNA directed against a syngeneic but antigenically different tumor (BP/B/5) and BP/B/5/TA, with spleen cells plus CT 26 I-RNA and BP/B/5TA, or with spleen cells plus BP/B/5 l-RNA and CT-26 TA, no anti-tumor effect was observed. These results indicate that the anti-tumor responses observed were due to tumor-specific immune responses. In conclusion, in order to obtain growth retardation or regression of established CT-26 tumor transplants, the sequential administration of all three agents (spleen cells, l-RNA and TA) was required. The optimal doses of each agent were found to be 1 X 10(7) spleen cells, 0.5 mg or 1 mg of l-RNA and 0.4 mg of tumor antigen. Higher or lower doses decreased the anti-tumor effect. Tumor-specific immune reactions appeared to be involved.</description><subject>Animals</subject><subject>Antigens, Neoplasm - immunology</subject><subject>Colonic Neoplasms - chemically induced</subject><subject>Colonic Neoplasms - therapy</subject><subject>Dose-Response Relationship, Immunologic</subject><subject>Immunotherapy - methods</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Neoplasm Transplantation</subject><subject>Neoplasms, Experimental - therapy</subject><subject>Nitrosomethylurethane</subject><subject>RNA - immunology</subject><subject>Spleen - immunology</subject><issn>0020-7136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotkE1LxDAYhHNQ1nX1Jwg5ebKQNF_tcVn8WFgUZO81ad-6kSapSYv039tle5qBeRiGuUJrQnKSKcrkDbpN6YcQSgXhK7SSVHEuyRp97Z0bfRhOEHU_4dBijd0YrQdchy54XGtfQ8R_djjhNPlv8GBrnPoOYA6h69ITtucOwJ_vW6x9g4fRhTi7wc70HbpudZfgftENOr48H3dv2eHjdb_bHrI-Z2rITElAS6WprEEZrUqlam5YIdrS5CQHYbjKOSetAVMY3QIQQQEk0LYxXLINerzU9jH8jpCGytl0nqc9hDFVVDAlSF7M4MMCjsZBU_XROh2nanmE_QORjV1U</recordid><startdate>19820101</startdate><enddate>19820101</enddate><creator>Fukushima, M</creator><creator>Colmerauer, M E</creator><creator>Nayak, S K</creator><creator>Koziol, J A</creator><creator>Pilch, Y H</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7T5</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>19820101</creationdate><title>Immunotherapy of a murine colon cancer with syngeneic spleen cells, immune RNA and tumor antigen</title><author>Fukushima, M ; Colmerauer, M E ; Nayak, S K ; Koziol, J A ; Pilch, Y H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p237t-b90ea67a16ce7ba7977c4b385f9b202e5b472440fbeb8bafee051ee6e1fdb463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>Animals</topic><topic>Antigens, Neoplasm - immunology</topic><topic>Colonic Neoplasms - chemically induced</topic><topic>Colonic Neoplasms - therapy</topic><topic>Dose-Response Relationship, Immunologic</topic><topic>Immunotherapy - methods</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Neoplasm Transplantation</topic><topic>Neoplasms, Experimental - therapy</topic><topic>Nitrosomethylurethane</topic><topic>RNA - immunology</topic><topic>Spleen - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fukushima, M</creatorcontrib><creatorcontrib>Colmerauer, M E</creatorcontrib><creatorcontrib>Nayak, S K</creatorcontrib><creatorcontrib>Koziol, J A</creatorcontrib><creatorcontrib>Pilch, Y H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fukushima, M</au><au>Colmerauer, M E</au><au>Nayak, S K</au><au>Koziol, J A</au><au>Pilch, Y H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunotherapy of a murine colon cancer with syngeneic spleen cells, immune RNA and tumor antigen</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>1982-01-01</date><risdate>1982</risdate><volume>29</volume><issue>1</issue><spage>107</spage><epage>112</epage><pages>107-112</pages><issn>0020-7136</issn><abstract>In combination with xenogeneic immune RNA (l-RNA) and tumor antigen (TA), syngeneic spleen cells inhibited the growth of a N-methyl-N-nitrosourethane-induced colon carcinoma (CT-26) in BALB/c mice. The sequential administration of 1 X 10(7) spleen cells, l mg of anti-CT-26 l-RNA and 0.4 mg of CT-26 TA resulted in a 20% survival rate of mice bearing established CT-26 tumors. On the other hand, administration of the spleen cells only, l-RNA only or TA only was not effective in inhibiting tumor growth. Similarly, when any one of the three agents (l-RNA, TA and spleen cells) was omitted, no anti-tumor effect was obtained. A higher dose (1 X 10(8) and a lower dose(1 X 10(6) of spleen cells decreased the anti-tumor effect of this combination therapy. A higher dose (2 mg) and a lower dose (0.5 mg) of l-RNA, as well as a higher dose of TA (0.8 mg) had no influence on the anti-tumor effect. However, a lower dose of TA (0.2 mg) in combination with spleen cells and l-RNA decreased the anti-tumor effect. When all three agents were administered at higher or lower doses, no anti-tumor effect was obtained. When mice bearing CT-26 tumors were treated with spleen cells, plus l-RNA directed against a syngeneic but antigenically different tumor (BP/B/5) and BP/B/5/TA, with spleen cells plus CT 26 I-RNA and BP/B/5TA, or with spleen cells plus BP/B/5 l-RNA and CT-26 TA, no anti-tumor effect was observed. These results indicate that the anti-tumor responses observed were due to tumor-specific immune responses. In conclusion, in order to obtain growth retardation or regression of established CT-26 tumor transplants, the sequential administration of all three agents (spleen cells, l-RNA and TA) was required. The optimal doses of each agent were found to be 1 X 10(7) spleen cells, 0.5 mg or 1 mg of l-RNA and 0.4 mg of tumor antigen. Higher or lower doses decreased the anti-tumor effect. Tumor-specific immune reactions appeared to be involved.</abstract><cop>United States</cop><pmid>6174460</pmid><tpages>6</tpages></addata></record> |
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subjects | Animals Antigens, Neoplasm - immunology Colonic Neoplasms - chemically induced Colonic Neoplasms - therapy Dose-Response Relationship, Immunologic Immunotherapy - methods Mice Mice, Inbred BALB C Neoplasm Transplantation Neoplasms, Experimental - therapy Nitrosomethylurethane RNA - immunology Spleen - immunology |
title | Immunotherapy of a murine colon cancer with syngeneic spleen cells, immune RNA and tumor antigen |
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