The Journal of Immunology · 1988 · 121 citations · 0 references
Veterinary MedicineInfectious DiseasesMicrobiologyHost-pathogen InteractionsImmunology Of Infectious DiseasesInnate ImmunityBacterial InfectionsCytokine BiologyImmune Responses To InfectionMacrophage BiologyAlveolar Macrophage FunctionAlveolar Macrophage ResponseCytokine Responses To Bacterial InfectionCytokine Signaling In InfectionLegionella InfectionLegionnaires' DiseaseMacrophage Responses To BacteriaPhagocyte Antimicrobial Activity
Human alveolar macrophages activated by human rIFN-gamma inhibit the intracellular multiplication of Legionella pneumophila, an intracellular bacterial pathogen and the agent of Legionnaires' disease. Activation of alveolar macrophages with IFN-gamma is dose dependent; significant inhibition of L. pneumophila multiplication (mean 1.60 +/- 0.20 logs) is achieved consistently with concentrations of IFN-gamma of greater than or equal to 2 x 10(-2) micrograms/ml (220 U/ml). Activation of alveolar macrophages is also time dependent. In macrophages treated continuously after explantation, macrophages infected at 48 to 96 h after explantation are more inhibitory than macrophages infected at 24 h after explantation. In macrophages not treated continuously after explantation but treated for various lengths of time before infection, the longer their exposure to IFN-gamma before infection, the greater the inhibition of L. pneumophila multiplication (96 greater than 72 greater than 48 greater than 24 h). IFN-gamma-activated alveolar macrophages exhibit morphologic signs of activation, including increased size, spreading, and aggregation. This paper demonstrates that a human resident macrophage can be activated with IFN-gamma such that it exhibits enhanced antimicrobial activity against a relevant pathogen.