Despite the unique functions of dendritic cells (DC), only two cell surface
antigens (CMRF-44 and CD83) with relatively restricted expression on human
DC have been described to date. We describe a third mAb, CMRF-56, which re
cognizes another DC early activation/differentiation antigen with limited e
xpression on other haemopoietic cell populations. Circulating blood leukocy
tes did not express the CMRF-56 antigen and following either in vitro cultu
re or activation of PBMC populations. CMRF-56 antigen expression was detect
ed only on DC and a subpopulation of CD19(+) lymphocytes. Circulating blood
DC were CMRF-56(-) but induced expression within 6 h of in vitro culture.
This, together with the finding that tonsil and synovial fluid DC upregulat
e the antigen following short-term in vitro culture, confirmed that CMRF-56
recognizes an early activation antigen on DC. Isolated Langerhan's cells,
dermal DC, migratory dermal DC and monocyte derived DC (GM-CSF/IL-4/TNF alp
ha) also espress the CMRF-56 antigen antigen modulation studies demonstrate
d that the amount of cell surface bound CMRF 56 and CMRF-44 (but not CD83)
mAb was dramatically reduced by short-term incubation at 37 degrees C. This
effect was not due to internalization and the reduction in CMRF-56 binding
was a reversible temperature-dependent process. In contrast, the decrease
in CMRF-44 binding was irreversible, suggesting that following ligation the
CMRF-44 antigen undergoes an irreversible conformational change or sheddin
g at 37 degrees C. Western blotting confirmed that CMRF-56 recognizes a pre
viously undescribed 95 kDa activation antigen whose cellular distribution a
nd expression kinetics overlaps with, but is clearly distinguishable from,
that that of the CD83 and CMRF-44 antigens. CMRF-56 therefore provides a us
eful additional marker for studies on human DC.