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Direct Effects of Type I Interferons on Cells of the Immune System

2011; American Association for Cancer Research; Volume: 17; Issue: 9 Linguagem: Inglês

10.1158/1078-0432.ccr-10-1114

1557-3265

Sandra Hervás‐Stubbs, Jose Luis Pérez‐Gracia, Ana Rouzaut, Miguel F. Sanmamed, Agnès Le Bon, Ignacio Melero,

T-cell and B-cell Immunology

Abstract Type I interferons (IFN-I) are well-known inducers of tumor cell apoptosis and antiangiogenesis via signaling through a common receptor interferon alpha receptor (IFNAR). IFNAR induces the Janus activated kinase–signal transducer and activation of transcription (JAK-STAT) pathway in most cells, along with other biochemical pathways that may differentially operate, depending on the responding cell subset, and jointly control a large collection of genes. IFNs-I were found to systemically activate natural killer (NK) cell activity. Recently, mouse experiments have shown that IFNs-I directly activate other cells of the immune system, such as antigen-presenting dendritic cells (DC) and CD4 and CD8 T cells. Signaling through the IFNAR in T cells is critical for the acquisition of effector functions. Cross-talk between IFNAR and the pathways turned on by other surface lymphocyte receptors has been described. Importantly, IFNs-I also increase antigen presentation of the tumor cells to be recognized by T lymphocytes. These IFN-driven immunostimulatory pathways offer opportunities to devise combinatorial immunotherapy strategies. Clin Cancer Res; 17(9); 2619–27. ©2011 AACR.