Alpha-interferon in hairy cell leukaemia: direct effects on hairy cells or indirect cytotoxicity? 1987

F Sigaux, and S Castaigne, and P Lehn, and E Dupuy, and C Billard, and J C Gluckman, and M Boiron, and E Falcoff, and G Flandrin, and L Degos

This report presents the results of a clinical trial on 53 patients with hairy cell leukaemia using low-dose alpha-interferon as therapy. Improvement of cytopenia and/or bone marrow hairy cell infiltration occurred in all but one patient. Often, blood and bone marrow improvements were dissociated and, after 7 or 13 months of therapy, complete remission was only observed in about 40% of patients. Recurrence of the disease was observed in some cases after cessation of therapy. A summary of the following results is presented: alpha-interferon receptor analysis, oncogene expression, study of the sensitivity of hairy cells to natural killer cells, and the effects of interferon on T-cell receptor gene rearrangement and on the function of T-cell clones. Results are also presented which show that myelofibrosis may be due to a release of platelet derived growth factor. The immunological findings and oncogene expression in 2 patients with a variant form of hairy cell leukaemia for which resistance to therapy was observed are also described. All the results show that interferon acts on hairy cells and are consistent with a direct effect by interferon in the treatment of hairy cell leukaemia.

UI MeSH Term Description Entries
D007370 Interferon Type I Interferon secreted by leukocytes, fibroblasts, or lymphoblasts in response to viruses or interferon inducers other than mitogens, antigens, or allo-antigens. They include alpha- and beta-interferons (INTERFERON-ALPHA and INTERFERON-BETA). Interferons Type I,Type I Interferon,Type I Interferons,Interferon, Type I,Interferons, Type I
D007694 Killer Cells, Natural Bone marrow-derived lymphocytes that possess cytotoxic properties, classically directed against transformed and virus-infected cells. Unlike T CELLS; and B CELLS; NK CELLS are not antigen specific. The cytotoxicity of natural killer cells is determined by the collective signaling of an array of inhibitory and stimulatory CELL SURFACE RECEPTORS. A subset of T-LYMPHOCYTES referred to as NATURAL KILLER T CELLS shares some of the properties of this cell type. NK Cells,Natural Killer Cells,Cell, NK,Cell, Natural Killer,Cells, NK,Cells, Natural Killer,Killer Cell, Natural,NK Cell,Natural Killer Cell
D007943 Leukemia, Hairy Cell A neoplastic disease of the lymphoreticular cells which is considered to be a rare type of chronic leukemia; it is characterized by an insidious onset, splenomegaly, anemia, granulocytopenia, thrombocytopenia, little or no lymphadenopathy, and the presence of "hairy" or "flagellated" cells in the blood and bone marrow. Hairy Cell Leukemia,Leukemic Reticuloendotheliosis,Reticuloendotheliosis, Leukemic,Hairy Cell Leukemias,Leukemias, Hairy Cell,Leukemic Reticuloendothelioses,Reticuloendothelioses, Leukemic
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009857 Oncogenes Genes whose gain-of-function alterations lead to NEOPLASTIC CELL TRANSFORMATION. They include, for example, genes for activators or stimulators of CELL PROLIFERATION such as growth factors, growth factor receptors, protein kinases, signal transducers, nuclear phosphoproteins, and transcription factors. A prefix of "v-" before oncogene symbols indicates oncogenes captured and transmitted by RETROVIRUSES; the prefix "c-" before the gene symbol of an oncogene indicates it is the cellular homolog (PROTO-ONCOGENES) of a v-oncogene. Transforming Genes,Oncogene,Transforming Gene,Gene, Transforming,Genes, Transforming
D011994 Recombinant Proteins Proteins prepared by recombinant DNA technology. Biosynthetic Protein,Biosynthetic Proteins,DNA Recombinant Proteins,Recombinant Protein,Proteins, Biosynthetic,Proteins, Recombinant DNA,DNA Proteins, Recombinant,Protein, Biosynthetic,Protein, Recombinant,Proteins, DNA Recombinant,Proteins, Recombinant,Recombinant DNA Proteins,Recombinant Proteins, DNA
D001792 Blood Platelets Non-nucleated disk-shaped cells formed in the megakaryocyte and found in the blood of all mammals. They are mainly involved in blood coagulation. Platelets,Thrombocytes,Blood Platelet,Platelet,Platelet, Blood,Platelets, Blood,Thrombocyte
D001853 Bone Marrow The soft tissue filling the cavities of bones. Bone marrow exists in two types, yellow and red. Yellow marrow is found in the large cavities of large bones and consists mostly of fat cells and a few primitive blood cells. Red marrow is a hematopoietic tissue and is the site of production of erythrocytes and granular leukocytes. Bone marrow is made up of a framework of connective tissue containing branching fibers with the frame being filled with marrow cells. Marrow,Red Marrow,Yellow Marrow,Marrow, Bone,Marrow, Red,Marrow, Yellow
D003602 Cytotoxicity, Immunologic The phenomenon of target cell destruction by immunologically active effector cells. It may be brought about directly by sensitized T-lymphocytes or by lymphoid or myeloid "killer" cells, or it may be mediated by cytotoxic antibody, cytotoxic factor released by lymphoid cells, or complement. Tumoricidal Activity, Immunologic,Immunologic Cytotoxicity,Immunologic Tumoricidal Activities,Immunologic Tumoricidal Activity,Tumoricidal Activities, Immunologic

Related Publications

F Sigaux, and S Castaigne, and P Lehn, and E Dupuy, and C Billard, and J C Gluckman, and M Boiron, and E Falcoff, and G Flandrin, and L Degos
February 1986, The New Zealand medical journal,
F Sigaux, and S Castaigne, and P Lehn, and E Dupuy, and C Billard, and J C Gluckman, and M Boiron, and E Falcoff, and G Flandrin, and L Degos
January 1991, European journal of cancer (Oxford, England : 1990),
F Sigaux, and S Castaigne, and P Lehn, and E Dupuy, and C Billard, and J C Gluckman, and M Boiron, and E Falcoff, and G Flandrin, and L Degos
February 1988, European journal of cancer & clinical oncology,
F Sigaux, and S Castaigne, and P Lehn, and E Dupuy, and C Billard, and J C Gluckman, and M Boiron, and E Falcoff, and G Flandrin, and L Degos
April 1989, The New Zealand medical journal,
F Sigaux, and S Castaigne, and P Lehn, and E Dupuy, and C Billard, and J C Gluckman, and M Boiron, and E Falcoff, and G Flandrin, and L Degos
July 1985, Scandinavian journal of haematology,
F Sigaux, and S Castaigne, and P Lehn, and E Dupuy, and C Billard, and J C Gluckman, and M Boiron, and E Falcoff, and G Flandrin, and L Degos
November 1987, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde,
F Sigaux, and S Castaigne, and P Lehn, and E Dupuy, and C Billard, and J C Gluckman, and M Boiron, and E Falcoff, and G Flandrin, and L Degos
May 1990, British journal of haematology,
F Sigaux, and S Castaigne, and P Lehn, and E Dupuy, and C Billard, and J C Gluckman, and M Boiron, and E Falcoff, and G Flandrin, and L Degos
January 1988, Acta haematologica,
F Sigaux, and S Castaigne, and P Lehn, and E Dupuy, and C Billard, and J C Gluckman, and M Boiron, and E Falcoff, and G Flandrin, and L Degos
June 1992, British journal of haematology,
F Sigaux, and S Castaigne, and P Lehn, and E Dupuy, and C Billard, and J C Gluckman, and M Boiron, and E Falcoff, and G Flandrin, and L Degos
October 1985, The New Zealand medical journal,
Copied contents to your clipboard!