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TLR7 agonist in combination with
We evaluated a novel approach combining the use of attenuated immunotherapy with a Toll-like receptor agonist, imiquimod, in B16F1 melanoma-bearing mice. B16F1 melanoma-bearing mice were daily treated with topical imiquimod in combination with one intratumoral injection of attenuated serovar Typhimu...
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Published in: | Immunotherapy 2018-06, Vol.10 (8), p.665-679 |
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container_issue | 8 |
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container_title | Immunotherapy |
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creator | Vola, Magdalena Mónaco, Amy Bascuas, Thais Rimsky, Geraldine Agorio, Caroline Isabel Chabalgoity, José Alejandro Moreno, María |
description | We evaluated a novel approach combining the use of attenuated
immunotherapy with a Toll-like receptor agonist, imiquimod, in B16F1 melanoma-bearing mice.
B16F1 melanoma-bearing mice were daily treated with topical imiquimod in combination with one intratumoral injection of attenuated
serovar Typhimurium LVR01.
The combined therapy resulted in retarded tumor growth and prolonged survival. Combination treatment led to an enhancement in the expression of pro-inflammatory cytokines and chemokines in the tumor microenvironment, with a Th1-skewed profile, resulting in a broad antitumor response. The induced immunity was effective in controlling the occurrence of metastasis.
LVR01 immunotherapy in combination with imiquimod is a novel approach that could be considered as an effective antimelanoma therapy. |
doi_str_mv | 10.2217/imt-2017-0188 |
format | article |
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immunotherapy with a Toll-like receptor agonist, imiquimod, in B16F1 melanoma-bearing mice.
B16F1 melanoma-bearing mice were daily treated with topical imiquimod in combination with one intratumoral injection of attenuated
serovar Typhimurium LVR01.
The combined therapy resulted in retarded tumor growth and prolonged survival. Combination treatment led to an enhancement in the expression of pro-inflammatory cytokines and chemokines in the tumor microenvironment, with a Th1-skewed profile, resulting in a broad antitumor response. The induced immunity was effective in controlling the occurrence of metastasis.
LVR01 immunotherapy in combination with imiquimod is a novel approach that could be considered as an effective antimelanoma therapy.</description><identifier>ISSN: 1750-743X</identifier><identifier>EISSN: 1750-7448</identifier><identifier>DOI: 10.2217/imt-2017-0188</identifier><language>eng</language><publisher>Future Medicine Ltd</publisher><subject>experimental model ; imiquimod ; immunotherapy ; melanoma</subject><ispartof>Immunotherapy, 2018-06, Vol.10 (8), p.665-679</ispartof><rights>2018 Future Medicine Ltd</rights><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>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Vola, Magdalena</creatorcontrib><creatorcontrib>Mónaco, Amy</creatorcontrib><creatorcontrib>Bascuas, Thais</creatorcontrib><creatorcontrib>Rimsky, Geraldine</creatorcontrib><creatorcontrib>Agorio, Caroline Isabel</creatorcontrib><creatorcontrib>Chabalgoity, José Alejandro</creatorcontrib><creatorcontrib>Moreno, María</creatorcontrib><title>TLR7 agonist in combination with</title><title>Immunotherapy</title><description>We evaluated a novel approach combining the use of attenuated
immunotherapy with a Toll-like receptor agonist, imiquimod, in B16F1 melanoma-bearing mice.
B16F1 melanoma-bearing mice were daily treated with topical imiquimod in combination with one intratumoral injection of attenuated
serovar Typhimurium LVR01.
The combined therapy resulted in retarded tumor growth and prolonged survival. Combination treatment led to an enhancement in the expression of pro-inflammatory cytokines and chemokines in the tumor microenvironment, with a Th1-skewed profile, resulting in a broad antitumor response. The induced immunity was effective in controlling the occurrence of metastasis.
LVR01 immunotherapy in combination with imiquimod is a novel approach that could be considered as an effective antimelanoma therapy.</description><subject>experimental model</subject><subject>imiquimod</subject><subject>immunotherapy</subject><subject>melanoma</subject><issn>1750-743X</issn><issn>1750-7448</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNpjYBA1NNAzMjI018_MLdE1MjA01zUwtLBgYuA0NDc10DU3MbFggbONIzgYuIqLswwMzEzMzUw4GRRCfILMFRLT8_Myi0sUMvMUkvNzkzLzEksy8_MUyjNLMngYWNMSc4pTeaE0N4Olm2uIs4duWmlJaVFqcXJmal5yajyEl5uakpmcmZcab2gQD3JSPNBJ8SAnxYOcZEyJXgCoq0L7</recordid><startdate>20180601</startdate><startdate>20180301</startdate><enddate>20180601</enddate><enddate>20180301</enddate><creator>Vola, Magdalena</creator><creator>Mónaco, Amy</creator><creator>Bascuas, Thais</creator><creator>Rimsky, Geraldine</creator><creator>Agorio, Caroline Isabel</creator><creator>Chabalgoity, José Alejandro</creator><creator>Moreno, María</creator><general>Future Medicine Ltd</general><scope/></search><sort><creationdate>20180601</creationdate><title>TLR7 agonist in combination with</title><author>Vola, Magdalena ; Mónaco, Amy ; Bascuas, Thais ; Rimsky, Geraldine ; Agorio, Caroline Isabel ; Chabalgoity, José Alejandro ; Moreno, María</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-futurescience_futuremedicine_10_2217_imt_2017_01883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>experimental model</topic><topic>imiquimod</topic><topic>immunotherapy</topic><topic>melanoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vola, Magdalena</creatorcontrib><creatorcontrib>Mónaco, Amy</creatorcontrib><creatorcontrib>Bascuas, Thais</creatorcontrib><creatorcontrib>Rimsky, Geraldine</creatorcontrib><creatorcontrib>Agorio, Caroline Isabel</creatorcontrib><creatorcontrib>Chabalgoity, José Alejandro</creatorcontrib><creatorcontrib>Moreno, María</creatorcontrib><jtitle>Immunotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vola, Magdalena</au><au>Mónaco, Amy</au><au>Bascuas, Thais</au><au>Rimsky, Geraldine</au><au>Agorio, Caroline Isabel</au><au>Chabalgoity, José Alejandro</au><au>Moreno, María</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>TLR7 agonist in combination with</atitle><jtitle>Immunotherapy</jtitle><date>2018-06-01</date><date>2018-03-01</date><risdate>2018</risdate><risdate>2018</risdate><volume>10</volume><issue>8</issue><spage>665</spage><epage>679</epage><pages>665-679</pages><issn>1750-743X</issn><eissn>1750-7448</eissn><abstract>We evaluated a novel approach combining the use of attenuated
immunotherapy with a Toll-like receptor agonist, imiquimod, in B16F1 melanoma-bearing mice.
B16F1 melanoma-bearing mice were daily treated with topical imiquimod in combination with one intratumoral injection of attenuated
serovar Typhimurium LVR01.
The combined therapy resulted in retarded tumor growth and prolonged survival. Combination treatment led to an enhancement in the expression of pro-inflammatory cytokines and chemokines in the tumor microenvironment, with a Th1-skewed profile, resulting in a broad antitumor response. The induced immunity was effective in controlling the occurrence of metastasis.
LVR01 immunotherapy in combination with imiquimod is a novel approach that could be considered as an effective antimelanoma therapy.</abstract><pub>Future Medicine Ltd</pub><doi>10.2217/imt-2017-0188</doi></addata></record> |
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language | eng |
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source | PubMed Central |
subjects | experimental model imiquimod immunotherapy melanoma |
title | TLR7 agonist in combination with |
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