Establishment of an IL-2-dependent cell line derived from 'nasal-type' NK/T-cell lymphoma of CD2(+), sCD3(-), CD3 epsilon(+), CD56(+) phenotype and associated with the Epstein-Barr virus
Y. Kagami et al., Establishment of an IL-2-dependent cell line derived from 'nasal-type' NK/T-cell lymphoma of CD2(+), sCD3(-), CD3 epsilon(+), CD56(+) phenotype and associated with the Epstein-Barr virus, BR J HAEM, 103(3), 1998, pp. 669-677
A novel interleukin-2 (IL-2)-dependent cell line, HANK1, was established fr
om a patient with CD56(+) NK/T-cell lymphoma arising in the retroperitoneum
. Morphologically, HANK1 is a pleomorphic large cell line with irregular nu
clei, which contains azurophilic granules in the cytoplasm. Immunophenotypi
c analysis showed that HANK1 expressed CD2, CD3 epsilon, CD56, TIA-1, granz
yme B, and HLA-DR, but no other T-lineage markers. These features were the
same as seen in the original tumour, and are highly characteristic of nasal
and 'nasal-type' NK/T-cell lymphoma as described in the proposed W.H.O. cl
assification. Genotypically this cell line also demonstrated the germline c
onfiguration of the T-cell receptor beta, gamma and the immunoglobulin heav
y chain genes and clonal integration of the Epstein-Barr virus (EBV) togeth
er with antigen expression with a type II latency pattern (LMP-1(+) and EBN
A2(-)). Furthermore, Southern blot analysis using the EBV termini as probes
confirmed its derivation from the original lymphoma, and revealed that it
contained multiple copies of the EBV genome. Dose-dependent growth on IL-2
was observed in an in vitro study with a doubling time of 3 d at maximal st
imulation. These data indicate that HANK1 seemed to preserve the biological
characteristics of the original tumour and therefore may serve as a good m
odel for the further analysis of unusual 'nasal-type' NK/T-cell lymphoma.