Abstract

BackgroundLiver perfusate (LP) lymphocytes show unique subsets compared with peripheral blood (PB) lymphocytes. LP natural killer (NK) and NKT cells may display unique cytotoxicity and cytokine production, thus leading to distinct roles in liver transplantation. In this study, we sought to evaluate the functions of graft perfusate NK and NKT cells in clinical liver transplantation. MethodsThe living donor right lobe graft was initially washed with 1 L of histidine-tryptophan-ketoglutarate solution to collect the perfusate. We also collected donor PB. Lymphocytes separated by the Ficoll-Hypaque density gradient method underwent immunophenotyping using multicolor flow cytometry. To assess cytokine secretion, we performed the enzyme-linked immunosorbent assay. ResultsThere were more NK and NKT cells in LP confirming previous reports. In particular, CD56brightCD16low NK cells accounted for approximately 50% of total NK cells compared with 5% to 10% among PB NK cells. In response to cytokine stimulation LP NK cells produce tumor necrosis factor–α at different levels and less interleukin-10 compared with PB NK cells. The major source of interferon-γ production upon stimulation with liver caner cells were CD56dim NK cells and CD56−CD3− cells rather than NKT or T cells. Unlike PB NK cells, LP CD56brightCD16low NK cells along with CD56dimCD16high NK cells and NKT cells were efficient killers against Korean liver cancer cells. ConclusionLP NK and NKT cells showed unique functions in cytotoxicity and cytokine production.

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