M. Oka et al., THE CHARACTERIZATION OF PERITONEAL AND PLEURAL EXUDATE CELLS FROM MALIGNANT EFFUSIONS, SURGERY TODAY-THE JAPANESE JOURNAL OF SURGERY, 23(6), 1993, pp. 500-503
The immune function of peripheral blood cells and cells from the pleur
al and abdominal effusions of patients with advanced cancer was compar
ed to that of peripheral blood cells from controls. The parameters exa
mined included lymphocyte subsets, natural killer (NK) cell activity,
and anti-Daudi and lymphokine-activated killer (LAK) cell activity. Th
e percentage of CD4+ pleural and peritoneal exudate cells (PEC) was si
gnificantly higher than the percentage of peripheral blood mononuclear
cells (PBMC) in the patients. The percentage of CD8+CD11+ PEC and PBM
C, being the suppressor T-cells, of the patients was increased compare
d with controls, while the percentage of CD8+CD11- PEC, being the cyto
toxic T-cells, was identical to the PBMC of both patients and controls
. The NK activity of PEC was significantly lower than that of PBMC in
both patients and controls, and there was no correlation between the N
K activity of PBMC and PEC. Although the anti-Daudi activity of PEC wa
s markedly low, LAK cells with high activity could be induced by cultu
re with interleukin-2 for 4 days. These results suggest that the immun
e function of cells in malignant effusions may be depressed due to a l
ow population of cytotoxic T cells, low NK activity and increased supp
ressor T cells, while the local administration of interleukin-2 may in
duce LAK cells. Therefore, effective local immunotherapy for malignant
effusions should not only augment effector cells, but also inhibit su
ppressor cells.