2020 Fiscal Year Final Research Report
Regulation of oxidative metabolic product-mediated immune suppressive tumor microenvironment to improve the efficacy of immune checkpoint blockade therapy in cancers.
Project/Area Number |
19K16808
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Research Category |
Grant-in-Aid for Early-Career Scientists
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Allocation Type | Multi-year Fund |
Review Section |
Basic Section 50020:Tumor diagnostics and therapeutics-related
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Research Institution | Keio University |
Principal Investigator |
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Project Period (FY) |
2019-04-01 – 2021-03-31
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Keywords | VAP-1 inhibitor / Immunosuppression / H2O2 / CTLs / ICIs |
Outline of Final Research Achievements |
Immunotherapy is a promising treatment modality for cancer. In this study we showed that inhibition of vascular adhesion protein 1, partly responsible for generating immunosuppressive microenvironment, can reverse the unfavorable immune-environment and synergize with current approve immunotherapy.
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Free Research Field |
Tumor immunotherapy
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Academic Significance and Societal Importance of the Research Achievements |
This study showed that oxidative tumor microenvironment can generate immunosuppressive element. This immunosuppression can be altered by inhibiting a particular adhesion protein. This information may help to revise patient care for immunotherapy.
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