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10.3389/fimmu.2016.00088

http://scihub22266oqcxt.onion/10.3389/fimmu.2016.00088
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C4789364!4789364!27014268
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suck abstract from ncbi


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pmid27014268      Front+Immunol 2016 ; 7 (ä): ä
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  • TLR3 Signaling Promotes the Induction of Unique Human BDCA-3 Dendritic Cell Populations #MMPMID27014268
  • Colletti NJ; Liu H; Gower AC; Alekseyev YO; Arendt CW; Shaw MH
  • Front Immunol 2016[]; 7 (ä): ä PMID27014268show ga
  • Conventional and plasmacytoid dendritic cells (cDCs and pDCs) are the two populations of DCs that can be readily identified in human blood. Conventional DCs have been subdivided into CD1c+, or blood dendritic cells antigen (BDCA) 1 and CD141+, or BDCA-3, DCs, each having both unique gene expression profiles and functions. BDCA-3 DCs express high levels of toll-like receptor 3 and upon stimulation with Poly I:C secrete IFN-?, CXCL10, and IL-12p70. In this article, we show that activation of human BDCA-3 DCs with Poly I:C induces the expression of activation markers (CD40, CD80, and CD86) and immunoglobulin-like transcript (ILT) 3 and 4. This Poly I:C stimulation results in four populations identifiable by flow cytometry based on their expression of ILT3 and ILT4. We focused our efforts on profiling the ILT4? and ILT4+ DCs. These ILT-expressing BDCA-3 populations exhibit similar levels of activation as measured by CD40, CD80, and CD86; however, they exhibit differential cytokine secretion profiles, unique gene signatures, and vary in their ability to prime allogenic naïve T cells. Taken together, these data illustrate that within a pool of BDCA-3 DCs, there are cells poised to respond differently to a given input stimulus with unique output of immune functions.
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