4.8 Article

NK-cell responses are biased towards CD16-mediated effector functions in chronic hepatitis B virus infection

Journal

JOURNAL OF HEPATOLOGY
Volume 70, Issue 3, Pages 351-360

Publisher

ELSEVIER
DOI: 10.1016/j.jhep.2018.10.006

Keywords

NK cells; Chronic hepatitis B virus infection; Human cytomegalovirus; CD16; Memory-like; Adaptive

Funding

  1. German Research Foundation (DFG) [SFB 1160/IMPATH, SFB/TRR 179]
  2. Else-Kroner-Fresenius Stiftung (MD graduate program MOTIVATE)
  3. Deutsche Krebshilfe [70112233]
  4. Infect-ERA grant [BMBF 031L0090]

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Background & Aims: Phenotypic and functional natural killer (NK)-cell alterations are well described in chronic hepatitis B virus (cHBV) infection. However, it is largely unknown whether these alterations result from general effects on the overall NK-cell population or the emergence of distinct NK-cell subsets. Human cytomegalovirus (HCMV) is common in cHBV and is associated with the emergence of memory-like NK cells. We aimed to assess the impact of these cells on cHBV infection. Methods: To assess the impact of memory-like NK cells on phenotypic and functional alterations in cHBV infection, we performed in-depth analyses of circulating NK cells in 52 patients with cHBV, 45 with chronic hepatitis C virus infection and 50 healthy donors, with respect to their HCMV serostatus. Results: In patients with cHBV/HCMV+, Fc epsilon RI gamma- memory-like NK cells were present in higher frequencies and with higher prevalence than in healthy donors with HCMV+. This pronounced HCMV-associated memory-like NK-cell expansion could be identified as key determinant of the NK-cell response in cHBV infection. Furthermore, we observed that memory-like NK cells consist of epigenetically distinct subsets and exhibit key metabolic characteristics of long-living cells. Despite ongoing chronic infection, the phenotype of memory-like NK cells was conserved in patients with cHBV/HCMV+. Functional characteristics of memory-like NK cells also remained largely unaffected by cHBV infection with the exception of an increased degranulation capacity in response to CD16 stimulation that was, however, detectable in both memory-like and conventional NK cells. Conclusions: The emergence of HCMV-associated memory-like NK cells shapes the overall NK-cell response in cHBV infection and contributes to a general shift towards CD16-mediated effector functions. Therefore, HCMV coinfection needs to be considered in the design of immunotherapeutic approaches that target NK cells in cHBV. Lay summary: In chronic hepatitis B virus infection, natural killer (NK)-cell phenotype and function is altered. In this study, we demonstrate that these changes are linked to the emergence of a distinct NK-cell subset, namely memory-like NK cells. The emergence of these memory-like NK cells is associated with coinfection of human cytomegalovirus that affects the majority of patients with chronic hepatitis B. (C) 2018 European Association for the Study of the Liver. Published by Elsevier B.V.

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