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10.18632/oncotarget.11755

http://scihub22266oqcxt.onion/10.18632/oncotarget.11755
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C5308624!5308624 !27590513
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suck abstract from ncbi


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pmid27590513
      Oncotarget 2016 ; 7 (38 ): 60896-60905
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  • Activation and selective IL-17 response of human V?9V?2 T lymphocytes by TLR-activated plasmacytoid dendritic cells #MMPMID27590513
  • Lo Presti E ; Caccamo N ; Orlando V ; Dieli F ; Meraviglia S
  • Oncotarget 2016[Sep]; 7 (38 ): 60896-60905 PMID27590513 show ga
  • V?9V?2 T cells and plasmacytoid dendritic cells (pDCs) are two distinct cell types of innate immunity that participate in early phases of immune response. We investigated whether a close functional relationship exists between these two cell populations using an in vitro co-culture in a human system.pDCs that had been activated by IL-3 and the TLR9 ligand CpG induced substantial activation of V?9V?2 T cells upon co-culture, which was cell-to-cell contact dependent, as demonstrated in transwell experiments, but that did not involve any of the costimulatory molecules potentially expressed by pDCs or V?9V2 T cells, such as ICOS-L, OX40 and CD40L. Activated pDCs selectively induced IL-17, but not IFN-?, responses of V?9V?2T cells, which was dominant over the antigen-induced response, and this was associated with the expansion of memory (both central and effector memory) subsets of V?9V?2 T cells.Overall, our results provide a further piece of information on the complex relationship between these two populations of cells with innate immunity features during inflammatory responses.
  • |Antigen Presentation [MESH]
  • |CD40 Ligand/metabolism [MESH]
  • |Cell Communication [MESH]
  • |Cell Proliferation [MESH]
  • |Coculture Techniques [MESH]
  • |CpG Islands [MESH]
  • |Dendritic Cells/*immunology [MESH]
  • |Humans [MESH]
  • |Immunity, Innate [MESH]
  • |Immunologic Memory [MESH]
  • |Inducible T-Cell Co-Stimulator Ligand/metabolism [MESH]
  • |Interferon-gamma/metabolism [MESH]
  • |Interleukin-17/*metabolism [MESH]
  • |Leukocytes, Mononuclear/cytology [MESH]
  • |Ligands [MESH]
  • |Lymphocyte Activation/*immunology [MESH]
  • |Phenotype [MESH]
  • |Receptors, OX40/metabolism [MESH]


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