D. Mitropoulos et al., CHARACTERIZATION OF FRESH (UNCULTURED) TUMOR-INFILTRATING LYMPHOCYTES(TIL) AND TIL-DERIVED T-CELL LINES FROM PATIENTS WITH RENAL-CELL CARCINOMA, Clinical and experimental immunology, 97(2), 1994, pp. 321-327
Fresh (uncultured) TIL from 12 untreated patients with primary renal c
ell carcinoma were prepared from tumour specimens by enzymatic digesti
on, and were characterized by immunofluorescence using MoAbs recognizi
ng leucocyte differentiation antigens or particular V alpha or V beta
segments of the T cell receptor (TCR). These fresh TIL comprised CD3() (20-84%); CD4(+) (3-15%); CD8(+) (13-35%); alpha beta TCR(+) (20-50%
); gamma delta TCR(+) (3-17%); CD16(+) (1-18%) and CD56(+) (3-10%) cel
ls. Significant proportions of V alpha 2(+), V beta 5.1(+) and V beta
6(+) cells were found in TIL of certain patients with renal cell carci
noma, suggesting that they comprised oligoclonal T cells. T cell lines
were developed in low concentrations of rIL-2 (200 U/ml) from TIL fro
m 11 patients with renal cell carcinoma, and were characterized by imm
unofluorescence and cell-mediated cytotoxicity. These T cell lines con
sisted primarily of CD3(+) (51-94%); CD4(+) (1-80%); CD8(+) (0-84%); a
lpha beta TCR(+) (65-87%); gamma delta TCR(+) (0-25%); CD16(+) (0-16%)
and CD56(+) (2-57%) cells. These T cell lines exhibited non-specific
cytotoxicity against autologous and allogeneic renal tumour cells, wit
h the exception of one T cell line that exhibited preferential cytotox
icity against autologous renal tumour cells. These results suggest tha
t fresh TIL from patients with renal cell carcinoma contain significan
t proportions of oligoclonal T cells that may have accumulated at the
tumour site as a result of a clonal expansion.