Variable expression of CD3-zeta chain in tumor-infiltrating lymphocytes (TIL) derived from renal-cell carcinoma: relationship with TIL phenotype and function

Int J Cancer. 1995 Oct 9;63(2):205-12. doi: 10.1002/ijc.2910630210.

Abstract

It has been reported that in mice and in humans, tumor-infiltrating lymphocytes (TIL) may exhibit a defect in CD3-zeta-chain expression. Therefore, the level of CD3-zeta was analyzed in TIL derived from patients with renal-cell carcinoma, and its correlation with TIL phenotype and function was assessed. We identified 4 out of 13 tumor-infiltrating lymphocytes derived from renal-cell carcinoma, with a significant decrease in CD3-zeta-chain expression as compared with control peripheral-blood lymphocytes. This defect was never found after culturing TIL with IL2. In one case, the low expression of zeta chain observed in TIL on day 0 was reversed when TIL were cultured with IL2. The zeta-chain level did not seem to predict the growth of TIL in response to IL2. All the TIL, irrespective of the level of zeta-chain expression, exhibited lower proliferative response when stimulated with PHA or anti-CD3 MAb in comparison with normal peripheral-blood mononuclear cells. Nevertheless, in this limited series of patients, a correlation was observed between the level of zeta-chain expression and T-cell infiltration (p = 0.02). After TIL stimulation with PHA or anti-CD3, in contrast to IL2 or IFN-gamma production, a trend towards a relationship between TNF alpha induction and the level of zeta-chain expression was observed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD3 Complex / chemistry
  • CD3 Complex / metabolism*
  • Carcinoma, Renal Cell / immunology*
  • Humans
  • Interferon-gamma / biosynthesis
  • Interleukin-2 / biosynthesis
  • Interleukin-2 / pharmacology
  • Kidney Neoplasms / immunology*
  • Killer Cells, Lymphokine-Activated / immunology
  • Lymphocyte Activation
  • Lymphocytes, Tumor-Infiltrating / metabolism*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • CD3 Complex
  • Interleukin-2
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma