摘要：SummaryMacrophages promote an early host response to infection by releasing pro-inflammatory cytokines such as interleukin-1β (IL-1β), TNF, and IL-6. The bioactivity of IL-1β is classically dependent on NLRP3 inflammasome activation, which culminates in caspase-1 activation and pyroptosis. Recent studies suggest a role for NLRP3 inflammasome activation in lung inflammation and fibrosis in both COVID-19 and SARS, and there is evidence of NLRP3 involvement in HIV-1 disease. Here, we show that GU-rich single-stranded RNA (GU-rich RNA) derived from SARS-CoV-2, SARS-CoV-1, and HIV-1 trigger a TLR8-dependent pro-inflammatory cytokine response from human macrophages in the absence of pyroptosis, with GU-rich RNA from the SARS-CoV-2 spike protein triggering the greatest inflammatory response. Using genetic and pharmacological inhibition, we show that the induction of mature IL-1β is through a non-classical pathway dependent on caspase-1, caspase-8, the NLRP3 inflammasome, potassium efflux, and autophagy while being independent of TRIF (TICAM1), vitamin D3, and pyroptosis.Graphical abstractDisplay OmittedHighlights•GU-rich ssRNA induces IL-1β, TNF, and IL-6 from human macrophages through TLR8•SARS-CoV-2 RNA elicits a greater inflammatory response than SARS-CoV-1 or HIV-1 RNA•SARS-CoV-2 RNA elicits TLR8-mediated IL-1β production in the absence of pyroptosis•TLR8-mediated IL-1β release is dependent on CASP8, K+ efflux, NLRP3, and autophagyImmunology; Virology
