Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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A novel tumor-associated myeloid cell population inhibits antigen-specific immune responses in cancer patients


ABSTRACT: Tumor progression is associated with an immunosuppressive microenvironment that consists of several elements, such as regulatory T cells, type 2 macrophages and myeloid-derived suppressor cells. Here, we identify for the first time a BDCA1+CD14+ population of immunosuppressive cells that resides both in the blood and tumor of melanoma patients. We demonstrated that the presence of these cells in dendritic cell (DC)-based anti-tumor vaccines significantly suppresses CD4+ T cells in an antigen-specific manner. In an attempt to reveal the mechanism of this suppressive activity, we noticed that BDCA1+CD14+ cells express elevated levels of the check-point molecule PD-L1, which thereby hinders T cell proliferation. Importantly, although this suppressive BDCA1+CD14+ population expresses markers o

ORGANISM(S): Homo sapiens

SUBMITTER: Ghaith Bakdash 

PROVIDER: E-GEOD-75042 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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