Infection of human synovial cells by human T cell lymphotropic virus type I. Proliferation and granulocyte/macrophage colony-stimulating factor production by synovial cells

J Clin Invest. 1993 Oct;92(4):1957-66. doi: 10.1172/JCI116789.

Abstract

The present study was performed to clarify the relationship between human T cell lymphotropic virus type I (HTLV-I) infection and chronic inflammatory arthropathy. To determine the ability of HTLV-I to infect synovial cells and the effect on synovial cell proliferation, synovial cells were cocultured with the HTLV-I-producing T cell lines (MT-2 or HCT-1). After coculture with HTLV-I-infected T cells, the synovial cells expressed HTLV-I-specific core antigens, and HTLV-I proviral DNA was detected from the synovial cells by polymerase chain reaction. These cocultured synovial cells with HTLV-I-infected T cells proliferated more actively than the synovial cells cocultured with uninfected T cells. This stimulatory effect of HTLV-I-infected T cells on synovial cell proliferation seems necessary to contact each other. After being cocultured with MT-2 cells, synovial cells proliferated more actively than control cells even after several passages. Furthermore, HTLV-I-infected synovial cells produced significant amounts of granulocyte/macrophage colony-stimulating factor. These results suggest that HTLV-I can infect synovial cells, resulting their active proliferation and may be involved in the pathogenesis of proliferative synovitis similar to that found in rheumatoid arthritis.

MeSH terms

  • Arthritis, Rheumatoid / metabolism
  • Arthritis, Rheumatoid / pathology
  • Cell Division
  • Cell Line
  • Cells, Cultured
  • Culture Media, Conditioned
  • DNA, Viral / analysis
  • Fluorescent Antibody Technique
  • Gene Products, gag / analysis
  • Gene Products, gag / biosynthesis
  • Granulocyte-Macrophage Colony-Stimulating Factor / biosynthesis*
  • Human T-lymphotropic virus 1 / physiology*
  • Humans
  • Immunoenzyme Techniques
  • Immunohistochemistry
  • Mitomycin / pharmacology
  • Polymerase Chain Reaction / methods
  • Proviruses / physiology
  • Synovial Membrane / cytology*
  • Synovial Membrane / drug effects
  • Synovial Membrane / metabolism*
  • T-Lymphocytes
  • Virus Replication

Substances

  • Culture Media, Conditioned
  • DNA, Viral
  • Gene Products, gag
  • Mitomycin
  • Granulocyte-Macrophage Colony-Stimulating Factor