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NK-cell responses are biased towards CD16-mediated effector functions in chronic hepatitis B virus infection.
Schuch, Anita; Zecher, Britta Franziska; Müller, Philipp Andreas; Correia, Margareta P; Daul, Franziska; Rennert, Charlotte; Tauber, Catrin; Schlitt, Karolin; Boettler, Tobias; Neumann-Haefelin, Christoph; Hengel, Hartmut; Pircher, Hanspeter; Cerwenka, Adelheid; Thimme, Robert; Hofmann, Maike.
Affiliation
  • Schuch A; Department of Medicine II, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg 79106, Germany; Faculty of Biology, University of Freiburg, Schänzlestraße 1, Freiburg 79104, Germany.
  • Zecher BF; Department of Medicine II, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg 79106, Germany.
  • Müller PA; Department of Medicine II, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg 79106, Germany.
  • Correia MP; Innate Immunity Group, German Cancer Research Center, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.
  • Daul F; Department of Medicine II, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg 79106, Germany; Faculty of Biology, University of Freiburg, Schänzlestraße 1, Freiburg 79104, Germany.
  • Rennert C; Department of Medicine II, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg 79106, Germany.
  • Tauber C; Department of Medicine II, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg 79106, Germany; Faculty of Biology, University of Freiburg, Schänzlestraße 1, Freiburg 79104, Germany.
  • Schlitt K; Department of Medicine II, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg 79106, Germany.
  • Boettler T; Department of Medicine II, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg 79106, Germany.
  • Neumann-Haefelin C; Department of Medicine II, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg 79106, Germany.
  • Hengel H; Institute of Virology, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hermann-Herder-Straße 11, Freiburg 79104, Germany.
  • Pircher H; Institute for Immunology, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hermann-Herder-Straße 11, Freiburg 79104, Germany.
  • Cerwenka A; Innate Immunity Group, German Cancer Research Center, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany; Department of Immunobiochemistry, University of Heidelberg, Medical Faculty Mannheim, Ludolf-Krehl-Strasse 13-17, Mannheim 68167, Germany.
  • Thimme R; Department of Medicine II, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg 79106, Germany.
  • Hofmann M; Department of Medicine II, University Hospital Freiburg - Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, Freiburg 79106, Germany. Electronic address: maike.hofmann@uniklinik-freiburg.de.
J Hepatol ; 70(3): 351-360, 2019 03.
Article in En | MEDLINE | ID: mdl-30342116
ABSTRACT
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+, FcεRIγ- 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.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Killer Cells, Natural / Lymphocyte Subsets / Receptors, IgG / Cytomegalovirus Infections / Hepatitis B, Chronic / Adaptive Immunity Type of study: Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Middle aged Language: En Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: Killer Cells, Natural / Lymphocyte Subsets / Receptors, IgG / Cytomegalovirus Infections / Hepatitis B, Chronic / Adaptive Immunity Type of study: Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Middle aged Language: En Year: 2019 Type: Article