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HLA‐DR + NK cells are mostly characterized by less mature phenotype and high functional activity
Author(s) -
Erokhina Sofya A,
Streltsova Maria A,
Kanevskiy Leonid M,
Telford William G,
Sapozhnikov Alexander M,
Kovalenko Elena I
Publication year - 2018
Publication title -
immunology and cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.999
H-Index - 104
eISSN - 1440-1711
pISSN - 0818-9641
DOI - 10.1111/imcb.1032
Subject(s) - k562 cells , nkg2d , interleukin 21 , biology , degranulation , interleukin 12 , microbiology and biotechnology , cd86 , cytokine , immunology , t cell , chemistry , in vitro , cytotoxic t cell , immune system , leukemia , biochemistry , receptor
NK cells change their phenotype and functional characteristics during activation. In this work, we searched for a relationship of HLA‐DR expression with differentiation stages and functional activity of NK cells ex vivo and stimulated in vitro with IL‐2 challenged with gene modified feeder K562 cells expressing membrane‐bound IL‐21 (K562‐mbIL21). This stimulation technique has been described for NK cell expansion in clinical use. We have observed that HLA‐DR expression in freshly isolated circulating NK cells was mostly associated with less differentiated CD56 bright CD57 – cells, although in some individuals it could also be found in terminally differentiated CD57 + cells. Ex vivo HLA‐DR + NK cells possessed better capacity to produce IFN‐γ in response to cytokine stimulation compared to their HLA‐DR – counterparts. In vitro activation with IL‐2 and K562‐mbIL21 induces an increase in HLA‐DR‐positive NK cell proportion, again mostly among CD56 bright CD57 – NK cells. This happened in particular due to appearance of HLA‐DR + expression de novo in HLA‐DR‐negative cells. Acquired in vitro HLA‐DR expression was associated with NK cell proliferation activity, more intense cytokine‐induced IFN‐γ production, increased degranulation toward feeder cells, and higher expression of CD86 and NKG2D. Thus, stimulation with IL‐2/K562‐mbIL21 causes a significant phenotype and functional shift during NK cell activation and expansion.