Open AccessCharacterization of fresh (uncultured) tumour‐infiltrating lymphocytes (TIL) and TIL‐derived T cell lines from patients with renal cell carcinoma
Author(s) -
MITROPOULOS D.,
KOOI S.,
RODRIGUEZVILLANUEVA J.,
PLATSOUCAS C. D.
Publication year - 1994
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/j.1365-2249.1994.tb06088.x
Subject(s) - cd8 , t cell receptor , cd3 , t cell , cell culture , biology , cytotoxicity , cytotoxic t cell , gamma delta t cell , cd16 , antigen , microbiology and biotechnology , pathology , immunology , cancer research , medicine , immune system , in vitro , biochemistry , genetics
SUMMARY Fresh (uncultured) TIL from 12 untreated patients with primary renal cell carcinoma were prepared from tumour specimens by enzymatic digestion, and were characterized by immunotluorescence using MoAbs recognizing leucocyte differentiation antigens or particular Va or Vα segments of the T cell receptor (TCR). These fresh TIL comprised CD3+ (20–84%); CD4 + (3–15%); CD8 + (13–35%); α/βTCR + (20 50%); γδTCR+ (3–17%); CD16+ (1–18%) and CD56 + (3–10%) cells. Significant proportions of Vα2 + , Vβ5.1 + and Vβ6 + cells were found in TIL of certain patients with renal cell carcinoma, suggesting that they comprised oligoclonal T cells. T cell lines were developed in low concentrations of rIL‐2 (200 U/ml) from TIL from II patients with renal cell carcinoma, and were characterized by immunofluorescence and cell‐mediated cytotoxicity. These T cell lines consisted primarily of CD3 + (51–94%); CD4 + (1–80%); CD8+ (0–84%); αβ/3TCR+ (65–87%); γδTCR+ (0–25%); CDI6 + (0–16%) and CD56 + (2–57%) cells. These Tcell lines exhibited non‐specific cytotoxicity against autologous and aliogeneic renal tumour cells, with the exception of one T cell line that exhibited preferential cytotoxicity against autoiogous renal tumour cells. These results suggest that fresh TIL from patients with renal cell carcinoma contain significant proportions of oligoclonal T cells that may have accumulated at the tumour site as a result of a clonal expansion.