Dw. Visscher et al., FLOW CYTOMETRIC ENUMERATION AND KINETIC-ANALYSIS OF INFLAMMATORY CELL-POPULATIONS IN BREAST CARCINOMAS, Analytical cellular pathology, 5(6), 1993, pp. 321-330
Inflammatory cell populations were quantitated in 76 consecutive mecha
nically dissociated clinical breast carcinoma specimens using multipar
ameter, two-color (PI-cytokeratin/FITC, PI-LCA/FITC) flow cytometric a
nalysis. The percent LCA-positive events varied from 1.3-62.5% (mean =
11%) and correlated with degree of histologic inflammatory cell infil
trate (mild-5.8% LCA + events vs. marked-35.9%. LCA + events, P < 0.00
1), abnormal DNA content (diploid range - 4.6% LCA + events vs. aneupl
oid - 13.3% LCA + events, P = 0.003) and poor tumor differentiation (w
ell-moderate - 6.5% LCA + events vs. poor - 19.9% LCA + events, P = 0.
001). Synthesis phase fractions in LCA-positive populations were unifo
rmly less than the corresponding cytokeratin (CK)-positive cells (mean
LCA + SPF = 4.4% vs. mean CK + SPF = 15.5%) and varied from 3-11%. Pr
oliferation among inflammatory populations did not correlate statistic
ally with the total percent of LCA or CK-positive events, nor with the
SPF in epithelial populations. However, proliferative activity of inf
lammatory components was greater in tumors with predominately intratum
oral, vs. peritumoral, inflammatory cell distribution (4.6% vs. 3.3% P
= 0.03) and in,tumors with greater numbers.of large, 'transformed' ly
mphocytes (few = 3.25% vs. many = 6.5% LCA + SPF, P = 0.001). We concl
ude multiparameter flow cytometric analysis of mechanically-dissociate
d breast tumors is representative of tumor infiltrating lymphoid popul
ations in breast tumors and provides a potentially useful means of stu
dying biologically relevant tumor-host interactions.