C1q reprograms innate immune memory [ChIP-seq]

Innate immune memory, also called trained immunity, is a metabolic and epigenetically regulated process that enables innate immune cells to recalibrate their inflammatory reactivity in response to pathogenic or endogenous stimuli. In addition to its function in host defense, trained immunity contributes to diverse immune-mediated diseases. We discovered that complement component 1q (C1q) is an effective modulator of innate immune memory, potently suppressing the responsiveness of myeloid cells. We found that C1q leads to profound reprogramming of myeloid cell metabolism, particularly glycolysis, and exerts control over the transcriptional regulation of important metabolic and inflammatory genes. We corroborate our findings by identifying single-nucleotide polymorphisms close to the C1q gene that are linked to induction of trained immunity in healthy volunteers. Our results reveal a novel immunomodulatory role for C1q and provide evidence of a molecular interaction between the complement system and innate immune memory. These findings expand our understanding of innate immune memory and provide a promising new target for therapeutic intervention. Overall design: Investigate the effects of C1q stimulation on the epigenome of monocytes. Therefore, we stimulated PBMCs with C1q or RPMI medium as control (n=4), and isolated monocytes on day 6 for a comprehensive genome-wide analysis of H3K4me3 through chromatin immunoprecipitation sequencing (ChIP-seq)