Characterization of a novel human natural killer-cell line (NK-YS) established from natural killer cell lymphoma/leukemia associated with Epstein-Barr virus infection

Blood. 1998 Aug 15;92(4):1374-83.

Abstract

A novel cell line was established from a patient with a leukemic-state nasal angiocentric natural killer (NK) cell lymphoma with systemic skin infiltration. The morphology of the leukemic cells was large-granular-lymphocyte (LGL), and their immunophenotype was CD2+, CD3-, CD5+, CD7+, CD16-, CD56+, and CD57-. The presence of Epstein-Barr viral (EBV) genome was shown in specimens from the patient's nose, skin, and peripheral blood by in situ hybridization using an EBV-encoded small RNA-1 probe or by Southern blotting using a terminal-repeat probe of the EBV genome. Leukemic cells were cocultured with a mouse stromal cell line (SPY3-2) in the presence of 100 U/mL recombinant human interleukin-2 and a novel stromal cell-independent cell line, NK-YS, was established. The NK-YS cells showed LGL morphology and expressed surface CD2, CD5, CD7, CD25, CD56, and CD95. The NK-YS cells retained cytotoxicity against K562 and Jurkat cells. A Southern blotting using a terminal-repeat probe of EBV showed that NK-YS and fresh leukemic cells had a clonal EBV genome, whereas the T-cell receptor beta and gamma chain genes of NK-YS were not rearranged. In an immunocytochemical analysis, the NK-YS cells showed a type-II latent infection of EBV. The NK-YS cells preserved the original characteristics of NK cell lymphoma/leukemia and will be a useful tool for the study of biological characteristics of EBV-associated nasal angiocentric NK cell lymphoma/leukemia.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Animals
  • Antigens, CD / analysis
  • Antigens, Neoplasm / analysis
  • Coculture Techniques
  • Cytotoxicity, Immunologic
  • DNA, Viral / analysis
  • Epstein-Barr Virus Nuclear Antigens / biosynthesis
  • Epstein-Barr Virus Nuclear Antigens / genetics
  • Fatal Outcome
  • Female
  • Granuloma, Lethal Midline / pathology
  • Granuloma, Lethal Midline / virology
  • Herpesviridae Infections / pathology*
  • Herpesviridae Infections / virology
  • Herpesvirus 4, Human / isolation & purification*
  • Humans
  • Immunophenotyping
  • In Situ Hybridization
  • Interleukin-2 / pharmacology
  • Killer Cells, Natural / pathology*
  • Killer Cells, Natural / virology
  • Leukemia, Lymphocytic, Chronic, B-Cell / pathology*
  • Leukemia, Lymphocytic, Chronic, B-Cell / virology
  • Lymphomatoid Granulomatosis / pathology*
  • Lymphomatoid Granulomatosis / virology
  • Mice
  • Neoplastic Cells, Circulating / immunology
  • Neoplastic Cells, Circulating / pathology*
  • Nose Neoplasms / pathology*
  • Nose Neoplasms / virology
  • RNA, Messenger / analysis
  • RNA, Viral / analysis
  • Recombinant Proteins / pharmacology
  • Tumor Cells, Cultured* / drug effects
  • Tumor Cells, Cultured* / immunology
  • Tumor Cells, Cultured* / pathology
  • Tumor Cells, Cultured* / virology
  • Tumor Virus Infections / pathology*
  • Tumor Virus Infections / virology
  • Viral Matrix Proteins / biosynthesis
  • Viral Matrix Proteins / genetics

Substances

  • Antigens, CD
  • Antigens, Neoplasm
  • DNA, Viral
  • EBV-associated membrane antigen, Epstein-Barr virus
  • Epstein-Barr Virus Nuclear Antigens
  • Interleukin-2
  • RNA, Messenger
  • RNA, Viral
  • Recombinant Proteins
  • Viral Matrix Proteins