The class Ib HLA-G gene encodes for a molecule which is selectively ex
pressed in fetal placental cells. Fetomaternal tolerance could be part
ially explained by the interactions between HLA-G molecules and KIR re
ceptors of decidual NK cells. To determine whether the presence of HLA
-G antigens might constitute a factor of immune tolerance during the t
umoral process, we compared the expression of the HLA-G gene in normal
and malignant hematopoietic cells. Despite a HLA-G transcriptional ac
tivity in several lymphocytes and monocytes, no antigens are found at
the cell surface or in the cytosol using the specific HLA-G mAb, 87G.
This lack of expression does not appear modified in malignant hematopo
ietic cells. However, treatment of the monohistiocytic cell line U937
with different cytokines enabled the expression of HLA-G antigens to b
e induced. We suggest that the potential induction of HLA-G molecules
in monocytic malignant cells following secretion of cytokines may cons
titute a factor of immune tolerance in patients. Human Immunology 59,
524-528 (1998). (C) American Society for Histocompatibility and Immuno
genetics, 1998. Published by Elsevier Science Inc.