RRC ID 64979
著者 Shimizu K, Yamasaki S, Shinga J, Sato Y, Watanabe T, Ohara O, Kuzushima K, Yagita H, Komuro Y, Asakura M, Fujii S.
タイトル Systemic DC Activation Modulates the Tumor Microenvironment and Shapes the Long-Lived Tumor-Specific Memory Mediated by CD8+ T Cells.
ジャーナル Cancer Res
Abstract Strategies to reprogram the tumor microenvironment are being explored to improve cancer immunotherapy. In one approach, we have targeted dendritic cells (DC) to improve their function with adjuvant vector cells (aAVC) that are engineered from NKT ligand-loaded CD1d(+) allogeneic cells transfected with tumor antigen mRNAs. Here, we report the finding that this approach also programs local immune responses by establishing tertiary lymphoid structures (TLS), which include expanded antigen-specific CD8(+) T-cell clones, mobilized DCs, and normalized tumor vasculature. aAVC therapy also expanded specific Vβ-expressing antitumor T-cell clones, leading to the formation of long-term memory T cells. When combined with PD-1 blockade, aAVC infusion triggered regression of poorly immunogenic tumor cells that did not respond to PD-1 blockade alone, as well as expansion of antigen-specific CD8(+) T-cell clones in the tumor. The findings of this study help to inform a next-generation platform for the generation of efficacious cancer vaccines. Cancer Res; 76(13); 3756-66. ©2016 AACR.
巻・号 76(13)
ページ 3756-66
公開日 2016-7-1
DOI 10.1158/0008-5472.CAN-15-3219
PII 76/13/3756
PMID 27371739
MeSH Adjuvants, Immunologic Animals Antigens, Neoplasm CD8-Positive T-Lymphocytes / immunology* Cancer Vaccines / immunology* Dendritic Cells / immunology* Female Humans Immunologic Memory / immunology* Immunotherapy Lymphocyte Activation Male Melanoma, Experimental / immunology Melanoma, Experimental / pathology Melanoma, Experimental / therapy* Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, Transgenic Tumor Cells, Cultured Tumor Microenvironment / immunology* Xenograft Model Antitumor Assays
IF 9.727
リソース情報
ヒト・動物細胞 NIH3T3