ci-959 and Paraparesis--Tropical-Spastic

ci-959 has been researched along with Paraparesis--Tropical-Spastic* in 1 studies

Other Studies

1 other study(ies) available for ci-959 and Paraparesis--Tropical-Spastic

ArticleYear
Marked suppression of T cells by a benzothiophene derivative in patients with human T-lymphotropic virus type I-associated myelopathy/tropical spastic paraparesis.
    Clinical and diagnostic laboratory immunology, 1999, Volume: 6, Issue:3

    In a search for new anti-autoimmune agents that selectively suppress activation of autoreactive T cells, one such agent, 5-methyl-3-(1-methylethoxy)benzo[b]thiophene-2-carboxamide (CI-959-A), was found to be effective. This compound, which is known to suppress tumor necrosis factor alpha (TNF-alpha)-induced CD54 expression, inhibited the primary proliferative response of the T cell to antigen (Ag)-presenting cells (APCs) including allogenic dendritic cells (DCs), autologous Epstein-Barr virus-infected B cells, and human T lymphotropic virus type I (HTLV-I)-infected T cells. Autoreactive T cells from patients with HTLV-I-associated myelopathy/tropical spastic paraparesis (HAM/TSP) spontaneously proliferate in vitro, and their activation is reported to be associated with CD54 expression. The spontaneous proliferation of T cells from patients with HAM/TSP was entirely blocked by CI-959-A. However, in this study, the T-cell proliferation in 15 patients with HAM/TSP was found to depend more extensively on major histocompatibility complex (MHC) class II and CD86 than on CD54 Ags. Since most important APCs for the development of HAM/TSP are DCs and HTLV-I-infected T cells, the effect of CI-959-A on DC generation and on the expression of surface molecules on activated T cells is examined. CI-959-A suppressed recombinant granulocyte-macrophage colony stimulating factor (GM-CSF)- and recombinant interleukin-4-dependent differentiation of DCs from monocytes and inhibited the expression of CD54 and, more extensively, MHC class II and CD86 Ags. CI-959-A showed little toxicity toward lymphoma or HTLV-I-infected T-cell lines or toward monocytes and cultured DCs. These results suggest that CI-959-A might be a potent anti-HAM/TSP agent.

    Topics: Adult; Aged; Antigen-Presenting Cells; Antigens, CD; B7-2 Antigen; Cell Differentiation; Cell Survival; Cells, Cultured; Dendritic Cells; Female; Human T-lymphotropic virus 1; Humans; Intercellular Adhesion Molecule-1; Lymphocyte Activation; Male; Membrane Glycoproteins; Middle Aged; Paraparesis, Tropical Spastic; T-Lymphocytes; Tetrazoles; Thiophenes; Tumor Cells, Cultured

1999