C1q reprograms innate immune memory

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 by Bacillus Calmette-Guérin (BCG) or beta-glucan in healthy peripheral blood mononuclear cells. Our results reveal an 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.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-05-23
DOI
https://doi.org/10.3389/fimmu.2025.1515127
Citations
4
Primary Topic
Immune responses and vaccinations
Type
article
Field-Weighted Citation Impact
3.19

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article

C1q reprograms innate immune memory

Joost H.A. Martens, Luuk B. Hilbrands, Vasiliki Matzaraki, Maaike Jacobs et al.
4 citations
Frontiers in Immunology
Immune responses and vaccinations
3.19
article

C1q reprograms innate immune memory

Joost H.A. Martens, Luuk B. Hilbrands, Vasiliki Matzaraki, Maaike Jacobs, Leo A. B. Joosten, Musa M. Mhlanga, Julia I. P. van Heck, Marijke Baltissen, Raphaël Duivenvoorden, Y. Negishi, Michiel Vermeulen, Abraham J. P. Teunissen, Inge Jonkman, Nils Rother, Willem J. M. Mulder, Mihai G. Netea, Zahi A. Fayad
article en
4 citations

Abstract

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 by Bacillus Calmette-Guérin (BCG) or beta-glucan in healthy peripheral blood mononuclear cells. Our results reveal an 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.

Frontiers in ImmunologyVol. 16
University of Bonn (DE), Radboud University Nijmegen (NL), Iuliu Hațieganu University of Medicine and Pharmacy (RO), Radboud University Medical Center (NL), Radboud Institute for Molecular Life Sciences (NL), Eindhoven University of Technology (NL), Icahn School of Medicine at Mount Sinai (US)
National Institute for Health and Care Research, Radboud Universiteit, Hartstichting, Nierstichting, Radboud Universitair Medisch Centrum, National Institutes of Health, European Research Council
Good health and well-being
Openalex Percentile: Top 8%
Immune responses and vaccinations
3.19
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