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Intratumoral induction of tumour necrosis factor by systemic administration of Bordetella pertussis vaccine
Intratumoral induction of tumour necrosis factor (TNF) by administration of Bordetella pertussis vaccine (BPV) as compared with that by the agent OK-432 was investigated in mice. Two hours after such administration tumour tissues tested were resected from the mice, homogenised, and the TNF activitie...
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Published in: | British journal of cancer 1990-09, Vol.62 (3), p.372-375 |
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creator | Minagawa, H Kobayashi, H Yoshida, H Teranishi, M Morikawa, A Abe, S Oshima, H Mizuno, D-I |
description | Intratumoral induction of tumour necrosis factor (TNF) by administration of Bordetella pertussis vaccine (BPV) as compared with that by the agent OK-432 was investigated in mice. Two hours after such administration tumour tissues tested were resected from the mice, homogenised, and the TNF activities in the homogenate were assayed using a L-929 fibroblast assay. Intravenous injection of BPV into mice bearing the MM46 carcinoma resulted in a greater concentration of TNF in the tumour homogenate than in the serum. With OK-432, however, there was a greater concentration of TNF in the serum than in the tumour homogenates. A high level of intratumoral TNF induction by BPV was also observed in mice bearing Meth A fibrosarcoma or Lewis lung carcinoma. The therapeutic effect against the Meth A fibrosarcoma was in parallel with the intratumoral TNF activity. Intratumoral TNF activity is therefore believed to be a good index of therapeutic effect. |
doi_str_mv | 10.1038/bjc.1990.300 |
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Two hours after such administration tumour tissues tested were resected from the mice, homogenised, and the TNF activities in the homogenate were assayed using a L-929 fibroblast assay. Intravenous injection of BPV into mice bearing the MM46 carcinoma resulted in a greater concentration of TNF in the tumour homogenate than in the serum. With OK-432, however, there was a greater concentration of TNF in the serum than in the tumour homogenates. A high level of intratumoral TNF induction by BPV was also observed in mice bearing Meth A fibrosarcoma or Lewis lung carcinoma. The therapeutic effect against the Meth A fibrosarcoma was in parallel with the intratumoral TNF activity. Intratumoral TNF activity is therefore believed to be a good index of therapeutic effect.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/bjc.1990.300</identifier><identifier>PMID: 2206945</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Animals ; Antibodies - pharmacology ; Antineoplastic agents ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Drug Administration Routes ; Drug Resistance ; Epidemiology ; experimental-oncology ; Female ; Fibrosarcoma - drug therapy ; Immunotherapy ; Macrophages - immunology ; Medical sciences ; Mice ; Mice, Inbred Strains ; Molecular Medicine ; Neoplasms, Experimental - drug therapy ; Neoplasms, Experimental - metabolism ; Oncology ; Pertussis Vaccine - administration & dosage ; Pertussis Vaccine - pharmacology ; Pharmacology. Drug treatments ; Picibanil - administration & dosage ; Picibanil - pharmacology ; Time Factors ; Tumor Necrosis Factor-alpha - metabolism</subject><ispartof>British journal of cancer, 1990-09, Vol.62 (3), p.372-375</ispartof><rights>Cancer Research Campaign 1990</rights><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-4f94e7ccce80fe3b8c5d8b3cf8a76dba740c01afd94040428f4871872a61af763</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971444/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971444/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27898,27899,53763,53765</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19748994$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2206945$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Minagawa, H</creatorcontrib><creatorcontrib>Kobayashi, H</creatorcontrib><creatorcontrib>Yoshida, H</creatorcontrib><creatorcontrib>Teranishi, M</creatorcontrib><creatorcontrib>Morikawa, A</creatorcontrib><creatorcontrib>Abe, S</creatorcontrib><creatorcontrib>Oshima, H</creatorcontrib><creatorcontrib>Mizuno, D-I</creatorcontrib><title>Intratumoral induction of tumour necrosis factor by systemic administration of Bordetella pertussis vaccine</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><addtitle>Br J Cancer</addtitle><description>Intratumoral induction of tumour necrosis factor (TNF) by administration of Bordetella pertussis vaccine (BPV) as compared with that by the agent OK-432 was investigated in mice. Two hours after such administration tumour tissues tested were resected from the mice, homogenised, and the TNF activities in the homogenate were assayed using a L-929 fibroblast assay. Intravenous injection of BPV into mice bearing the MM46 carcinoma resulted in a greater concentration of TNF in the tumour homogenate than in the serum. With OK-432, however, there was a greater concentration of TNF in the serum than in the tumour homogenates. A high level of intratumoral TNF induction by BPV was also observed in mice bearing Meth A fibrosarcoma or Lewis lung carcinoma. The therapeutic effect against the Meth A fibrosarcoma was in parallel with the intratumoral TNF activity. Intratumoral TNF activity is therefore believed to be a good index of therapeutic effect.</description><subject>Animals</subject><subject>Antibodies - pharmacology</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Drug Administration Routes</subject><subject>Drug Resistance</subject><subject>Epidemiology</subject><subject>experimental-oncology</subject><subject>Female</subject><subject>Fibrosarcoma - drug therapy</subject><subject>Immunotherapy</subject><subject>Macrophages - immunology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Molecular Medicine</subject><subject>Neoplasms, Experimental - drug therapy</subject><subject>Neoplasms, Experimental - metabolism</subject><subject>Oncology</subject><subject>Pertussis Vaccine - administration & dosage</subject><subject>Pertussis Vaccine - pharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Picibanil - administration & dosage</subject><subject>Picibanil - pharmacology</subject><subject>Time Factors</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNptUU2LFDEQDaKs4-rNq5CLnuyx0p2ZJBdhXfxYWPCi55CuTtaM3cmYpBfm35tmmlVBcihS79Wrj0fISwZbBp181x9wy5SCbQfwiGzYrmsbJlvxmGwAQDSgWnhKnuV8qF8FUlyQi7aFveK7Dfl5E0oyZZ5iMiP1YZix-BhodHRJzokGiylmn6kzWGKi_YnmUy528kjNMPng86KwFn2IabDFjqOhR5vKnJfKe4Pog31OnjgzZvtijZfk-6eP366_NLdfP99cX902yLkoDXeKW4GIVoKzXS9xN8i-QyeN2A-9ERwQmHGD4lBfKx2XgknRmn3Nin13Sd6fdY9zP9kB7bLiqI_JTyaddDRe_4sE_0PfxXvNlGCc8yrwZhVI8ddsc9GTz7gsFWycs5YALeOdrMS3Z-Jyopyse2jCQC_m6GqOXszR1ZxKf_X3YA_k1Y2Kv15xk9GMLpmAPv_RVIJLpZb5mjMvVyjc2aQP1alQb_r_vr8BiLCqyQ</recordid><startdate>19900901</startdate><enddate>19900901</enddate><creator>Minagawa, H</creator><creator>Kobayashi, H</creator><creator>Yoshida, H</creator><creator>Teranishi, M</creator><creator>Morikawa, A</creator><creator>Abe, S</creator><creator>Oshima, H</creator><creator>Mizuno, D-I</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19900901</creationdate><title>Intratumoral induction of tumour necrosis factor by systemic administration of Bordetella pertussis vaccine</title><author>Minagawa, H ; Kobayashi, H ; Yoshida, H ; Teranishi, M ; Morikawa, A ; Abe, S ; Oshima, H ; Mizuno, D-I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-4f94e7ccce80fe3b8c5d8b3cf8a76dba740c01afd94040428f4871872a61af763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Animals</topic><topic>Antibodies - pharmacology</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Drug Administration Routes</topic><topic>Drug Resistance</topic><topic>Epidemiology</topic><topic>experimental-oncology</topic><topic>Female</topic><topic>Fibrosarcoma - drug therapy</topic><topic>Immunotherapy</topic><topic>Macrophages - immunology</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Molecular Medicine</topic><topic>Neoplasms, Experimental - drug therapy</topic><topic>Neoplasms, Experimental - metabolism</topic><topic>Oncology</topic><topic>Pertussis Vaccine - administration & dosage</topic><topic>Pertussis Vaccine - pharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Picibanil - administration & dosage</topic><topic>Picibanil - pharmacology</topic><topic>Time Factors</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Minagawa, H</creatorcontrib><creatorcontrib>Kobayashi, H</creatorcontrib><creatorcontrib>Yoshida, H</creatorcontrib><creatorcontrib>Teranishi, M</creatorcontrib><creatorcontrib>Morikawa, A</creatorcontrib><creatorcontrib>Abe, S</creatorcontrib><creatorcontrib>Oshima, H</creatorcontrib><creatorcontrib>Mizuno, D-I</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Minagawa, H</au><au>Kobayashi, H</au><au>Yoshida, H</au><au>Teranishi, M</au><au>Morikawa, A</au><au>Abe, S</au><au>Oshima, H</au><au>Mizuno, D-I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intratumoral induction of tumour necrosis factor by systemic administration of Bordetella pertussis vaccine</atitle><jtitle>British journal of cancer</jtitle><stitle>Br J Cancer</stitle><addtitle>Br J Cancer</addtitle><date>1990-09-01</date><risdate>1990</risdate><volume>62</volume><issue>3</issue><spage>372</spage><epage>375</epage><pages>372-375</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><coden>BJCAAI</coden><abstract>Intratumoral induction of tumour necrosis factor (TNF) by administration of Bordetella pertussis vaccine (BPV) as compared with that by the agent OK-432 was investigated in mice. Two hours after such administration tumour tissues tested were resected from the mice, homogenised, and the TNF activities in the homogenate were assayed using a L-929 fibroblast assay. Intravenous injection of BPV into mice bearing the MM46 carcinoma resulted in a greater concentration of TNF in the tumour homogenate than in the serum. With OK-432, however, there was a greater concentration of TNF in the serum than in the tumour homogenates. A high level of intratumoral TNF induction by BPV was also observed in mice bearing Meth A fibrosarcoma or Lewis lung carcinoma. The therapeutic effect against the Meth A fibrosarcoma was in parallel with the intratumoral TNF activity. Intratumoral TNF activity is therefore believed to be a good index of therapeutic effect.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>2206945</pmid><doi>10.1038/bjc.1990.300</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibodies - pharmacology Antineoplastic agents Biological and medical sciences Biomedical and Life Sciences Biomedicine Cancer Research Drug Administration Routes Drug Resistance Epidemiology experimental-oncology Female Fibrosarcoma - drug therapy Immunotherapy Macrophages - immunology Medical sciences Mice Mice, Inbred Strains Molecular Medicine Neoplasms, Experimental - drug therapy Neoplasms, Experimental - metabolism Oncology Pertussis Vaccine - administration & dosage Pertussis Vaccine - pharmacology Pharmacology. Drug treatments Picibanil - administration & dosage Picibanil - pharmacology Time Factors Tumor Necrosis Factor-alpha - metabolism |
title | Intratumoral induction of tumour necrosis factor by systemic administration of Bordetella pertussis vaccine |
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