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NK cells generate memory‐type responses to human cytomegalovirus‐infected fibroblasts
Author(s) -
Newhook Nicholas,
Fudge Neva,
Grant Michael
Publication year - 2017
Publication title -
european journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.272
H-Index - 201
eISSN - 1521-4141
pISSN - 0014-2980
DOI - 10.1002/eji.201646819
Subject(s) - human cytomegalovirus , biology , cytotoxic t cell , interleukin 12 , interleukin 21 , lymphokine activated killer cell , natural killer cell , immunology , cytotoxicity , interferon , virology , in vitro , immune system , t cell , virus , biochemistry
Natural killer (NK) cells are cytotoxic lymphocytes that selectively respond against abnormal cells. Human cytomegalovirus (HCMV) infection causes expansion of NKG2C + CD57 + NK cells in vivo and NKG2C + NK cells proliferate when cultured with HCMV‐infected cells. This raises the possibility of an NK‐cell subset selectively responding against a specific pathogen and accruing memory. To test this possibility, we compared proliferation, natural cytotoxicity and interferon‐γ (IFN‐γ) production of NK cells from HCMV‐seropositive and HCMV‐seronegative individuals co‐cultured with HCMV‐infected or uninfected MRC‐5 cells. There was no significant difference in proliferation of NK cells from HCMV‐seropositive or seronegative individuals against uninfected MRC‐5 cells, but significantly more NK cells from the HCMV‐seropositive group proliferated in response to HCMV‐infected MRC‐5 cells. Natural cytotoxicity of NK cells against K562 cells increased following co‐culture with HCMV‐infected versus uninfected MRC‐5 only for the HCMV‐seropositive group. After co‐culture with HCMV‐infected MRC‐5 cells, proliferating NK cells from HCMV‐seropositive donors selectively produced IFN‐γ when re‐exposed to HCMV‐infected MRC‐5 cells. Both NKG2C + and NKG2C − NK cells proliferated in co‐culture with HCMV‐infected MRC‐5 cells, with the fraction of proliferating NKG2C + NK cells directly correlating with the circulating NKG2C + fraction. These data illustrate an at least partly NKG2C‐independent human NK‐cell memory‐type response against HCMV.