Expression of HLA G may be a way for tumor cells to escape immuno-surveilla
nce. HLA G is selectively expressed by extravillous trophoblast in the huma
n placenta, a tissue that does not express HLA A or B molecules. It is temp
ting to propose that tumor cells resemble this unique HLA class I phenotype
as they frequently lose classical HLA A, B and C class I expression. Such
peculiar HLA class I distribution would in theory allow tumor cells to esca
pe from T- and NK-cell cytotoxicity, To determine whether HLA G is expresse
d on tumor cells, we studied HLA G mRNA levers using RT-PCR and HLA G cell-
surface expression by immunohistological techniques in a panel of 50 human
solid tumor tissues, 31 tumor cell lines of different origin, 4 autologous
mucosa samples and 3 peripheral white cell samples. We found mRNA transcrip
ts of different HLA G isoforms in most of the samples studied. However, we
did not detect cell-surface expression of HLA G using 3 specific monoclonal
antibodies (MAbs; 87G, 01G and G223), HLA G was detected only in the U937
myelomanocytic cell line after stimulation with IFN-gamma. We favor the hyp
othesis that HLA G plays a minor role, if any, in providing an inhibitory s
ignal to NK cells to escape immunosurveillance. We cannot, however, exclude
the possibility that some other HLA G isoforms may he expressed in some tu
mors. (C) 1999 Wiley-Liss. Inc.