IL-15 Generates IFN-γ-producing Cells Reciprocally Expressing Lymphoid-Myeloid Markers during Dendritic Cell Differentiation

Abstract

Recently, interest in IL-15-differentiated cells has increased; however, the phenotypic definition of IL-15-differentiated bone marrow-derived cells (IL-15-DBMCs) is still under debate, particularly the generation of IFN--producing innate cells such as premature NK (pre-mNK) cells, natural killer dendritic cells (NKDCs), interferon-producing killer dendritic cells (IKDCs), and type 1 innate lymphoid cells (ILC1s), all of which are IL-15-dependent. Here, we revisited the immunophenotypic characteristics of IFN--producing IL-15-DBMCs and their functional role in the control of intracellular Mycobacterium tuberculosis (Mtb) infection. When comparing the cytokine levels between bone marrow-derived dendritic cells (BMDCs) and IL-15-DBMCs upon stimulation with various TLR agonists, only the CD11c int population of IL-15-DBMCs produced significant levels of IFN-, decreased levels of MHC-II, and increased levels of B220. Neither BMDCs nor IL-15-DBMCs were found to express DX5 or NK1.1, which are representative markers for the NK cell lineage and IKDCs. When the CD11c int B220 + population of IL-15-DBMCs was enriched, the Thy1.2 + Sca-1 + population showed a marked increase in IFN- production. In addition, while depletion of the B220 + and Thy1.2 + populations of IL-15-DBMCs, but not the CD19 + population, inhibited IFN- production, enrichment of these cell populations increased IFN-. Ultimately, co-culture of sorted IFN--producing B220 + Thy1.2 + IL-15-DBMCs with Mtb-infected macrophages resulted in control of the intracellular growth of Mtb via the IFN--nitric oxide axis in a donor cell number-dependent manner. Taken together, the results indicate that IFN--producing IL-15-DBMCs could be redefined as CD11c int B220 + Thy1.2 + Sca-1 + cells, which phenotypically resemble both IKDCs and ILC1s, and may have therapeutic potential for controlling infectious intracellular bacteria such as Mtb.