The present study undertook to investigate the biological significance
of human leucocyte antigen expression in hepatocellular carcinoma and
to elucidate the role of potential modulating agents on human leucocy
te antigen expression. These studies used several hepatic tumour-deriv
ed cell lines as in vitro model systems. The cell lines included PLC/P
RF/S (Alexander cell line), Hep3B, HepG2, TONG PHC, HA22T/VGH, HA59T/V
GH and Mahlavu. The cell lines K562 and Raji were used as negative and
positive controls, respectively. K562, a B lymphoid-derived cell line
, was shown to express negligible amounts of human leucocyte antigens,
while Raji, an erythromyeloid-derived cell line, expressed both class
I and class II human leucocyte antigens as well as their respective i
nvariant chains, beta(2)-microglobulin and Ii. Using an ELISA, experim
ents performed on these cell lines confirmed the natural expression of
class I and class II antigens by the HA22T/VGH and HA59T/VGH cell lin
es, whereas PLC/PRF/S displayed class II surface antigens only. The ef
fects of modulating agents such as interferon-gamma sodium butyrate an
d clofazimine on human leucocyte antigen expression were investigated
using the HA22T/VGH, HA59T/VGH and TONG PHC cell lines. These agents i
ncreased class I and class II human leucocyte antigen expression on HA
22T/VGH and TONG PHC cells, but had no effect on the HA59T/VGH cell li
ne. The results suggest a potential use for these agents as modulators
of human leucocyte antigen expression by human heptocellular cell lin
es.