Dendritic Cell-Based Immunotherapy for Glioma: Multiple Regimens and Implications in Clinical Trials
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- MINEHARU Yohei
- Division of Neuroendovascular Therapy, Institute of Biomedical Research and Innovation Departmemt of Neurosurgery, Kobe City Medical Center General Hospital
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- CASTRO Maria G
- Department of Neurosurgery, The University of Michigan School of Medicine Department of Cell and Developmental Biology, The University of Michigan School of Medicine
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- LOWENSTEIN Pedro R
- Department of Neurosurgery, The University of Michigan School of Medicine Department of Cell and Developmental Biology, The University of Michigan School of Medicine
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- SAKAI Nobuyuki
- Division of Neuroendovascular Therapy, Institute of Biomedical Research and Innovation Departmemt of Neurosurgery, Kobe City Medical Center General Hospital
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- MIYAMOTO Susumu
- Department of Neurosurgery, Kyoto University Graduate School of Medicine
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抄録
High grade glioma is a highly invasive brain tumor and recurrence is almost inevitable, even after radical resection of the tumor mass. Cytotoxic immune responses and immunological memory induced by immunotherapy might prevent tumor recurrence. Dendritic cells (DCs) are professional antigen-presenting cells of the innate immune system with the potential to generate robust antigen-specific T cell immune responses. DC-based immunotherapeutic strategies have been intensively studied in both preclinical and clinical settings. Although advances have been made in the experimental use of DCs, there are still considerable challenges that need to be addressed for clinical translation. In this review, we describe the variability of regimens currently available for DC-based immunotherapy and then review strategies to optimize DC therapeutic efficacy against glioma.
収録刊行物
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- Neurologia medico-chirurgica
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Neurologia medico-chirurgica 53 (11), 741-754, 2013
一般社団法人 日本脳神経外科学会
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詳細情報 詳細情報について
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- CRID
- 1390282680034403200
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- NII論文ID
- 10031196785
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- NII書誌ID
- AN00358613
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- COI
- 1:STN:280:DC%2BC2c%2Fot1ejtA%3D%3D
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- ISSN
- 13498029
- 04708105
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- PubMed
- 24140772
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可