As trophoblast cells and macrophages share cellular characteristics, we inv
estigated the expression of HLA-G antigens during the myelomonocytic differ
entiation. Analyses with the 87G and 16G1 monoclonal antibodies demonstrate
d that HLA-G was not expressed in peripheral blood monocytes, in in vitro d
ifferentiated dendritic cells and macrophages, and in resident mononuclear
phagocytes infiltrating healthy tissues. Conversely, activated macrophages
and dendritic cells localized in tumoral biopsies of some lung carcinomas e
xpressed HLA-G antigens. Induction of HLA-G expression at the cell surface
of the monohistiocytic cell line U 937 with different cytokines strongly su
ggests that cytokines secreted during inflammation may be involved in this
specific upregulation. Bronchoalveolar macrophages collected from patients
suffering from acute HCMV pneumonitis also expressed HLA-G molecules. In vi
tro, we thus demonstrated that HLA-G antigens are produced during viral rea
ctivation in the macrophages generated after allogeneic stimulation of HCMV
latently infected monocytes. Our data suggest that inflammatory processes
in lung tissues, like tumoral transformation and HCMV acute infection, are
likely to induce HLA-G molecules in infiltrating macrophages and dendritic
cells. The expression of molecules capable of downregulating both the innat
e and adoptive immunity could be a mechanism that helps tumoral and HCMV in
fected cells to escape immune response. (C) American Society for Histocompa
tibility and Immunogenetics, 2000. Published by Elsevier Science Inc.