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Therapeutic and tumor-specific immunity induced by combination of dendritic cells and oncolytic adenovirus expressing IL-12 and 4-1BBL

DC Field Value Language
dc.contributor.author김주항-
dc.contributor.author김호근-
dc.contributor.author윤채옥-
dc.contributor.author이민걸-
dc.contributor.author장송남-
dc.contributor.author최경주-
dc.contributor.author최일규-
dc.date.accessioned2015-04-23T16:28:45Z-
dc.date.available2015-04-23T16:28:45Z-
dc.date.issued2010-
dc.identifier.issn1525-0016-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/100657-
dc.description.abstractRecently, gene-based cytokine treatment has been actively pursued as a new promising approach in treating cancer. In an effort to augment the efficiency of antitumor effect by cytokine-mediated immunotherapy, we selected both interleukin (IL)-12 and 4-1BB ligand (4-1BBL) as suitable cytokines to fully activate the type-1 immune response. Coexpression of IL-12 and 4-1BBL mediated by oncolytic adenovirus (Ad) greatly enhanced the antitumor effect. Further, synergistic enhancement in interferon (IFN)-gamma levels were seen in mice treated with oncolytic Ad expressing both IL-12 and 4-1BBL. Next, to improve the overall antitumor immune response, we coadministered IL-12- and 4-1BBL-coexpressing oncolytic Ad with dendritic cells (DCs). Combination treatment of IL-12- and 4-1BBL-coexpressing oncolytic Ad and DCs elicited greater antitumor and antimetastatic effects than either treatment alone. Moreover, enhanced type-1 antitumor immune response and higher migratory abilities of DCs in tumors were also observed in the combination arms. The nature of the enhanced antitumor immune response seems to be mediated through the enhanced cytolytic activity of cytotoxic T lymphocytes (CTLs) and IFN-gamma-releasing immune cells. Taken together, these data highlight the potential therapeutic benefit of combining IL-12- and 4-1BBL-coexpressing oncolytic Ad with DCs and warrants further evaluation in the clinic.-
dc.description.statementOfResponsibilityopen-
dc.format.extent264~274-
dc.relation.isPartOfMOLECULAR THERAPY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESH4-1BB Ligand/genetics-
dc.subject.MESH4-1BB Ligand/immunology*-
dc.subject.MESH4-1BB Ligand/physiology-
dc.subject.MESHAdenoviridae/genetics-
dc.subject.MESHAdenoviridae/physiology*-
dc.subject.MESHAnimals-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHCells, Cultured-
dc.subject.MESHDendritic Cells/cytology-
dc.subject.MESHDendritic Cells/physiology*-
dc.subject.MESHHumans-
dc.subject.MESHIn Vitro Techniques-
dc.subject.MESHInterleukin-12/genetics-
dc.subject.MESHInterleukin-12/immunology*-
dc.subject.MESHInterleukin-12/physiology-
dc.subject.MESHMelanoma/immunology*-
dc.subject.MESHMelanoma/therapy*-
dc.subject.MESHMice-
dc.subject.MESHMice, Inbred C57BL-
dc.subject.MESHOncolytic Viruses/genetics-
dc.subject.MESHOncolytic Viruses/physiology*-
dc.titleTherapeutic and tumor-specific immunity induced by combination of dendritic cells and oncolytic adenovirus expressing IL-12 and 4-1BBL-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentMedical Research Center (임상의학연구센터)-
dc.contributor.googleauthorJing-Hua Huang-
dc.contributor.googleauthorSong-Nan Zhang-
dc.contributor.googleauthorKyung-Ju Choi-
dc.contributor.googleauthorIl-Kyu Choi-
dc.contributor.googleauthorJoo-Hang Kim-
dc.contributor.googleauthorMingul Lee-
dc.contributor.googleauthorHoguen Kim-
dc.contributor.googleauthorChae-Ok Yun-
dc.identifier.doi10.1038/mt.2009.205-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00945-
dc.contributor.localIdA01183-
dc.contributor.localIdA02614-
dc.contributor.localIdA02779-
dc.contributor.localIdA03442-
dc.contributor.localIdA04034-
dc.contributor.localIdA04168-
dc.relation.journalcodeJ02271-
dc.identifier.eissn1525-0024-
dc.identifier.pmid19738604-
dc.contributor.alternativeNameKim, Joo Hang-
dc.contributor.alternativeNameKim, Ho Keun-
dc.contributor.alternativeNameYun, Chae Ok-
dc.contributor.alternativeNameLee, Min Geol-
dc.contributor.alternativeNameZhang, Song Nan-
dc.contributor.alternativeNameChoi, Kyung Ju-
dc.contributor.alternativeNameChoi, Il Kyu-
dc.contributor.affiliatedAuthorKim, Joo Hang-
dc.contributor.affiliatedAuthorKim, Ho Keun-
dc.contributor.affiliatedAuthorYun, Chae Ok-
dc.contributor.affiliatedAuthorLee, Min Geol-
dc.contributor.affiliatedAuthorZhang, Song Nan-
dc.contributor.affiliatedAuthorChoi, Kyung Ju-
dc.contributor.affiliatedAuthorChoi, Il Kyu-
dc.citation.volume18-
dc.citation.number2-
dc.citation.startPage264-
dc.citation.endPage274-
dc.identifier.bibliographicCitationMOLECULAR THERAPY, Vol.18(2) : 264-274, 2010-
dc.identifier.rimsid37727-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Research Institute (부설연구소) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Dermatology (피부과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers

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