Bf. Banner et al., AN IMMUNOPHENOTYPIC STUDY OF THE INFLAMMATORY CELL-POPULATIONS IN COLON ADENOMAS AND CARCINOMAS, Modern pathology, 6(3), 1993, pp. 295-301
There is increasing interest in the host immunologic response to colon
carcinoma as immunotherapeutic techniques are being developed. We stu
died the inflammatory cells in 27 specimens of normal mucosa, 16 hyper
plastic polyps, 21 tubular adenomas, 19 tubulovillous adenomas, 12 vil
lous adenomas, and 17 invasive carcinomas using immunohistochemical te
chniques in paraffin-embedded tissue. UCHL-1-positive T-cells predomin
ated in the lamina propria of all specimens. In polyps and carcinomas,
reactive lymphoid follicles composed of L26-positive B-cells, and UCH
L-1-positive T-cells were a prominent feature and UCHL-1-positive cell
s were increased in the epithelial compartment. Cells bearing surface
immunoglobulins were widely distributed in all specimens, with IgA pre
dominating. There was a relative increase in IgG-positive cells in the
carcinomas. KP1-positive macrophages, S-100-positive dendritic cells,
and HLA-DR-positive cells were oriented toward the lumenal surface in
normal mucosa and hyperplastic polyps, suggesting a diffuse antigen p
resenting system. Macrophages and dendritic cells were increased and d
ispersed in the neoplasms. HLA-DR expression was increased in the neop
lasms, mainly in the stromal cells. We conclude that there is an activ
ated immune response in adenomas and carcinomas of the colon compared
to normal mucosa. This is represented by expansion and reorganization
of both the T- and B-cell compartments and the macrophage-cell systems
.