Differentiation-associated ISG expression of NK cells in chronic viral infection

Natural killer (NK) cell responses are modulated by type-I interferons (IFNs) in viral infection. Chronic hepatitis C virus (HCV) infection, marked by robust IFN signatures, shows NK cells with reduced cytokine release but heightened cytotoxicity. Comparable alterations occur in chronic hepatitis B virus (HBV) infection even without a pronounced IFN milieu, implying additional regulatory layers. We analyzed NK cells from healthy donors and patients with chronic HBV or HCV and found conserved expression patterns of interferon-stimulated genes (ISGs) such as <i>IFITM3</i>, <i>IRF1</i>, <i>IFIT2,</i> and <i>ISG20</i> that correlated with NK cell differentiation state. These genes are governed by fate-determining transcription factors, including ETS1, FLI1, and Eomes, and appear to be constitutively expressed rather than driven by persistent IFN exposure. Network analysis suggested that NK cell ISGs participate not only in antiviral defense but also in processes such as transport and metabolism, underscoring their role in shaping NK responses during health and chronic viral infection.

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Publication Details

Journal
iScience
Published
2025-07-26
DOI
https://doi.org/10.1016/j.isci.2025.113216
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
0.00

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article

Differentiation-associated ISG expression of NK cells in chronic viral infection

Giuseppe Rusignuolo, Timo B. Trefzer, Marta Rizzi, Franziska Maria Keller et al.
iScience
Immune Cell Function and Interaction
article

Differentiation-associated ISG expression of NK cells in chronic viral infection

Giuseppe Rusignuolo, Timo B. Trefzer, Marta Rizzi, Franziska Maria Keller, Christoph Neumann‐Haefelin, Bertram Bengsch, Marco Binder, Roland Eils, Robert Lorenz Chua, Maike Hofmann, Robert Thimme, Volker Lohmann, Katharina Jechow, Özlem Soğukpınar, Andreas Pichlmair, Tobias Boettler, Liane Bauersfeld, Fabian Beier, Christian Conrad, Sagar Sagar
article en

Abstract

Natural killer (NK) cell responses are modulated by type-I interferons (IFNs) in viral infection. Chronic hepatitis C virus (HCV) infection, marked by robust IFN signatures, shows NK cells with reduced cytokine release but heightened cytotoxicity. Comparable alterations occur in chronic hepatitis B virus (HBV) infection even without a pronounced IFN milieu, implying additional regulatory layers. We analyzed NK cells from healthy donors and patients with chronic HBV or HCV and found conserved expression patterns of interferon-stimulated genes (ISGs) such as <i>IFITM3</i>, <i>IRF1</i>, <i>IFIT2,</i> and <i>ISG20</i> that correlated with NK cell differentiation state. These genes are governed by fate-determining transcription factors, including ETS1, FLI1, and Eomes, and appear to be constitutively expressed rather than driven by persistent IFN exposure. Network analysis suggested that NK cell ISGs participate not only in antiviral defense but also in processes such as transport and metabolism, underscoring their role in shaping NK responses during health and chronic viral infection.

iScienceVol. 28(9)
University of Freiburg (DE), German Cancer Research Center (DE), Heidelberg University (DE), University Medical Center Freiburg (DE), Humboldt-Universität zu Berlin (DE), German Center for Infection Research (DE), University of Education Freiburg (DE), Berlin Institute of Health at Charité - Universitätsmedizin Berlin (DE), Protestant University of Applied Sciences Freiburg (DE), Technical University of Munich (DE)
Deutsche Forschungsgemeinschaft
Good health and well-being
Openalex Percentile: Top 80%
Immune Cell Function and Interaction
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