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2015 Fiscal Year Final Research Report

Analysis of antitumor immunity induced by vaccinia virus with in vivo imaging

Research Project

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Project/Area Number 25462254
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Neurosurgery
Research InstitutionKyoto University

Principal Investigator

Arakawa Yoshiki  京都大学, 医学(系)研究科(研究院), 助教 (20378649)

Co-Investigator(Kenkyū-buntansha) Dean Thumkeo  京都大学, 医学研究科, 助教 (40372594)
Co-Investigator(Renkei-kenkyūsha) Matsuda Michiyuki  京都大学, 医学研究科, 教授 (10199812)
Research Collaborator Murata Daiki  
Fujimoto Ko-ichi  
Yokogawa Ryuta  
Terada Yukinori  
Fukui Nobuyuki  
Liu Bin  
Project Period (FY) 2013-04-01 – 2016-03-31
Keywords悪性脳腫瘍 / ワクシニアウイルス / 生体イメージング
Outline of Final Research Achievements

The aim of the project is to analyze oncolytic bioresponse induced by vaccinia virus, and to develop the new oncolytic therapy. Our previous results indicate that the antitumor immunity activated by vaccinia virus is effective for malignant brain tumors. In brain tumor models, the induction of antitumor immune competent cells was identified by immunohistochemical staining and flow cytometry, although it was not sufficient for long-term tumor control. As Flt3L is known to be a strong stimulator of antitumor immune system, Flt3L-expressing vaccinia virus has been developed. The in vivo analyzing system of antitumor immunity has been prepared to evaluate efficacy of Flt3L-expressing vaccinia virus. The status of antitumor immunity in medulloblastoma was analyzed. We confirmed that high PD-L1 expression and low CD8+ lymphocyte infiltration was associated with worse survival in patients with medulloblastoma.

Free Research Field

脳神経外科

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Published: 2017-05-10  

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