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      Cross-talk between myeloid-derived suppressor cells (MDSC), macrophages, and dendritic cells enhances tumor-induced immune suppression.

      Seminars in Cancer Biology
      Animals, Dendritic Cells, immunology, metabolism, Humans, Immunotherapy, Inflammation, Inflammation Mediators, Macrophages, Myeloid Cells, Neoplasms, pathology, therapy, Tumor Escape, Tumor Microenvironment

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          Abstract

          The tumor microenvironment is a complex milieu of tumor and host cells. Host cells can include tumor-reactive T cells capable of killing tumor cells. However, more frequently the tumor and host components interact to generate a highly immune suppressive environment that frustrates T cell cytotoxicity and promotes tumor progression through a variety of immune and non-immune mechanisms. Myeloid-derived suppressor cells (MDSC) are a major host component contributing to the immune suppressive environment. In addition to their inherent immune suppressive function, MDSC amplify the immune suppressive activity of macrophages and dendritic cells via cross-talk. This article will review the cell-cell interactions used by MDSC to inhibit anti-tumor immunity and promote progression, and the role of inflammation in promoting cross-talk between MDSC and other cells in the tumor microenvironment. Copyright © 2012. Published by Elsevier Ltd.

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          Author and article information

          Journal
          22313874
          3701942
          10.1016/j.semcancer.2012.01.011

          Chemistry
          Animals,Dendritic Cells,immunology,metabolism,Humans,Immunotherapy,Inflammation,Inflammation Mediators,Macrophages,Myeloid Cells,Neoplasms,pathology,therapy,Tumor Escape,Tumor Microenvironment

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