Human monocyte-derived cytotoxic factors (CF) induced by dengue virus
were studied. Using several human leukemia cell lines as precursors, t
he biological activities of CF in conditioned medium from dengue virus
-infected monocytes were demonstrated through the measurement of tumor
cell growth inhibition. The conditioned medium from dengue virus infe
cted monocytes suppressed significantly growth of GEM, HL60, K562, and
U937 cells. In the presence of 10% conditioned medium (v/v) from deng
ue virus infected monocytes, DNA synthesis of U937 cells, as measured
by [H-3]thymidine incorporation, decreased by 99% in contrast to their
synthesis in conditioned medium from noninfected control monocytes, w
hich did not have any suppressive effect. Partial characterization of
CF showed that it is a proteinase-K-sensitive and heat-labile protein
with a molecular mass over 100 kDa. Employing a flow cytometric analys
is of the cell cycle, it was found that U937 cells, treated either wit
h conditioned medium from dengue virus infected monocytes or with CF,
but not treated with conditioned medium from noninfected monocytes, sh
owed cell-cycle arrest in G1 phase by 48 hr. This suppressive effect o
f CF on U937 growth was dose- and time-dependent. These results sugges
t that dengue virus-infected monocytes may produce CF to target myeloi
d cells, resulting in the hematological changes observed in patients w
ith dengue fever. (C) 1995 Wiley-Liss, Inc.