Soluble tumor necrosis factor receptor expression in patients with metastatic renal cell carcinoma treated with interleukin-2-based lmmunotherapy

  • Arie Belldegrun*
  • , William Pierce
  • , David Sayah
  • , Jean deKernion
  • , David Wallach
  • , Dan Aderka
  • , Robert A. Figlin
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Two distinct types of soluble tumor necrosis factor α receptors (sTNFRs), which are felt to represent proteolytic cleavage products of the extracellular domains of membrane-bound TNFRs of molecular mass, 55 and 75 kDa, are found in the serum and urine of humans. We have measured the serum concentrations of these receptors in eight patients with metastatic renal cell carcinoma during treatment with interleukin-2 (IL-2)-based immunotherapy. The mean pretreatment concentration of sTNFR-55 kDa (p <0.05) but not sTNFR-75 kDa was significantly elevated prior to the onset of immunotherapy. In one patient the concentrations of both sTNFRs decreased dramatically following removal of the primary tumor. There were significant increases in the concentrations of both sTNFRs in patients treated with IL-2-based therapy that included in vivo primed tumor infiltrating lymphocytes (pTILs); some of these patients eventually achieved a complete response to therapy. These data demonstrate that sTNFR-55 kDa is elevated in patients with metastatic renal cell carcinoma prior to therapy and that IL-2-based therapy that included pTIL cells results in a further increase in sTNFRs.

Original languageEnglish
Pages (from-to)175-180
Number of pages6
JournalJournal of Immunotherapy
Volume13
Issue number3
DOIs
StatePublished - Apr 1993
Externally publishedYes

Keywords

  • Metastatic renal cell carcinoma
  • Tumor necrosis factor a receptor-Interleukin-2
  • Tumor necrosis factor α

Fingerprint

Dive into the research topics of 'Soluble tumor necrosis factor receptor expression in patients with metastatic renal cell carcinoma treated with interleukin-2-based lmmunotherapy'. Together they form a unique fingerprint.

Cite this