Diversity of immunobiological functions of T-cell lines established from patients with adult T-cell leukaemia

Br J Dermatol. 1995 Dec;133(6):861-7. doi: 10.1111/j.1365-2133.1995.tb06917.x.

Abstract

In order to understand the variety of HTLV-1-associated cutaneous diseases, we studied the cytological profile of HTLV-1-infected T-cell lines established from patients with adult T-cell leukaemia (ATL). Among four CD4+ cell lines, termed 16T(-), 35T(-), MH-1, and KS-2, the 16T(-) cells secreted elevated quantities of IL-4, IL-6 and IFN-gamma and expressed mRNA for each cytokine in the absence of exogenous stimulation. The 35T(-) cells secreted IL-6 and a small amount of IFN-gamma, but not IL-4. The MH-1 and KS-2 cells secreted only IL-6 in the absence of stimulation. In response to stimulation with phorbol-12-myristate-13 acetate (PMA), the 16T(-) cells produced more IL-4 and IFN-gamma, whereas the 35T(-) and MH-1 cells exhibited increased secretion of IFN-gamma, but still no IL-4 or IL-4 mRNA production. Although neither IL-4 nor IFN-gamma were found in the culture supernatant of KS-2 cells, the production of IL-4 mRNA was detected by RT-PCR. Culture supernatants from the 16T(-) and 35T(-) cells induced the expression of intercellular adhesion molecule-1 (ICAM-1) and HLA-DR by cultured keratinocytes. This response was inhibited by pretreatment of the supernatant with anti-IFN-gamma antibodies. These results indicate that some HTLV-1-infected T-cell lines constitutively secrete various cytokines, including biologically active IFN-gamma. The diversity of immunobiological functions of the T-cell lines may be related to the variety of clinical features present in ATL patients.

MeSH terms

  • Adult
  • Antigens, Viral / analysis
  • Base Sequence
  • Cell Line
  • Culture Media, Conditioned / pharmacology
  • Cytokines / analysis
  • DNA Primers / genetics
  • DNA, Viral / analysis
  • HLA-DR Antigens / metabolism
  • Human T-lymphotropic virus 1* / genetics
  • Human T-lymphotropic virus 1* / immunology
  • Humans
  • Intercellular Adhesion Molecule-1 / metabolism
  • Keratinocytes / metabolism
  • Leukemia, T-Cell / immunology*
  • Leukemia, T-Cell / virology
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • RNA, Messenger / analysis
  • T-Lymphocytes / immunology*

Substances

  • Antigens, Viral
  • Culture Media, Conditioned
  • Cytokines
  • DNA Primers
  • DNA, Viral
  • HLA-DR Antigens
  • RNA, Messenger
  • Intercellular Adhesion Molecule-1