Hyaluronic acid-supported combination of water insoluble immunostimulatory compounds for anti-cancer immunotherapy

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dc.contributor.authorShin, Woo Jungko
dc.contributor.authorNoh, Hyun Jongko
dc.contributor.authorNoh, Young-Woockko
dc.contributor.authorKim, Sohyunko
dc.contributor.authorUm, Soong Hoko
dc.contributor.authorLim, Yong Taikko
dc.date.accessioned2023-03-17T03:00:35Z-
dc.date.available2023-03-17T03:00:35Z-
dc.date.created2023-03-17-
dc.date.created2023-03-17-
dc.date.created2023-03-17-
dc.date.issued2017-01-
dc.identifier.citationCARBOHYDRATE POLYMERS, v.155, pp.1 - 10-
dc.identifier.issn0144-8617-
dc.identifier.urihttp://hdl.handle.net/10203/305667-
dc.description.abstractA novel powder-form combination adjuvant system containing two immunostimulatory compounds was firstly developed and evaluated as a therapeutic intervention for cancer immunotherapy. With the help of hyaluronic acid (HA), water insoluble monophosphoryl lipid A (MPL), QS21 and imiquimod (R837), could be easily dispersed in aqueous solution and lyophilized as powder-form, which have an advantage in room-temperature storage stability compared with those conventional liquid formulation that requires cold storage. Two kinds of HA-based combination vaccine adjuvants (HA/MPL/QS21, HMQ and HA/MPL/R837, HMR) contributed to the increase of both humoral and cellular immunity, which is very important for efficient cancer immunotherapy. Through the challenge experiments in EG7-OVA (mouse lymphoma-expressing OVA) tumor-bearing mice model, we found out that the immunostimulatory effects of HMQ and HMR were successful in the inhibition of tumor proliferation. Taken together, both HA-based powder-form combination adjuvant systems are expected to be used as potent prophylactic and therapeutic cancer vaccine. (C) 2016 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCI LTD-
dc.titleHyaluronic acid-supported combination of water insoluble immunostimulatory compounds for anti-cancer immunotherapy-
dc.typeArticle-
dc.identifier.wosid000386402600001-
dc.identifier.scopusid2-s2.0-84983242579-
dc.type.rimsART-
dc.citation.volume155-
dc.citation.beginningpage1-
dc.citation.endingpage10-
dc.citation.publicationnameCARBOHYDRATE POLYMERS-
dc.identifier.doi10.1016/j.carbpol.2016.08.040-
dc.contributor.localauthorShin, Woo Jung-
dc.contributor.nonIdAuthorNoh, Hyun Jong-
dc.contributor.nonIdAuthorNoh, Young-Woock-
dc.contributor.nonIdAuthorKim, Sohyun-
dc.contributor.nonIdAuthorUm, Soong Ho-
dc.contributor.nonIdAuthorLim, Yong Taik-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorCancer immunotherapy-
dc.subject.keywordAuthorPowder-form adjuvant-
dc.subject.keywordAuthorImmunostimulation-
dc.subject.keywordAuthorHyaluronic acid-
dc.subject.keywordAuthorCellular immunity-
dc.subject.keywordPlusMONOPHOSPHORYL-LIPID-A-
dc.subject.keywordPlusIMMUNE-RESPONSES-
dc.subject.keywordPlusAGONIST IMIQUIMOD-
dc.subject.keywordPlusINFLUENZA VACCINE-
dc.subject.keywordPlusDENDRITIC CELLS-
dc.subject.keywordPlusTLR7 AGONIST-
dc.subject.keywordPlusADJUVANT-
dc.subject.keywordPlusOLIGONUCLEOTIDES-
dc.subject.keywordPlusENHANCEMENT-
dc.subject.keywordPlusINFECTION-
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