The Journal of Experimental Medicine · 2000 · 221 citations · 44 references
Life SciencesCell BiologyImmunologyAdaptive ImmunityDevelopmental ImmunologyInnate ImmunityAntiviral ImmunityDendritic Cell BiologyImmune Cell DifferentiationInnate Immune ActivationInnate Immune Cell DevelopmentInnate Immune ResponseAdaptive Immune Responses To Viral InfectionAntiviral Interferon ResponsesFetal Hematopoietic Stem CellsFlow Cytometry ImmunophenotypingHematopoietic Immune Cell DevelopmentInterferon ProductionInterferon Response To Viral InfectionInterferon-mediated Innate Immunity
Upon viral stimulation, the natural interferon (IFN)-alpha/beta-producing cells (IPCs; also known as pre-dendritic cells (DCs 2) in human blood and peripheral lymphoid tissues rapidly produce huge amounts of IFN-alpha/beta. After performing this innate antiviral immune response, IPCs can differentiate into DCs and strongly stimulate T cell-mediated adaptive immune responses. Using four-color immunofluorescence flow cytometry, we have mapped the developmental pathway of pre-DC2/IPCs from CD34(+) hematopoietic stem cells in human fetal liver, bone marrow, and cord blood. At least four developmental stages were identified, including CD34(++)CD45RA(-) early progenitor cells, CD34(++)CD45RA(+) late progenitor cells, CD34(+)CD45RA(++)CD4(+)interleukin (IL)-3Ralpha(++) pro-DC2, and CD34(-)CD45RA(++) CD4(+)IL-3Ralpha(++) pre-DC2/IPCs. Pro-DC2s have already acquired the capacity to produce large amounts of IFN-alpha/beta upon viral stimulation and to differentiate into DCs in culture with IL-3 and CD40 ligand. CD34(++)CD45RA(-) early progenitor cells did not have the capacity to produce large amounts of IFN-alpha/beta in response to viral stimulation; however, they can be induced to undergo proliferation and differentiation into IPCs/pre-DC2 in culture with FLT3 ligand.
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