INVIVO INTERLEUKIN-6 GENE-EXPRESSION IN THE TUMORAL ENVIRONMENT IN MULTIPLE-MYELOMA

被引:92
作者
PORTIER, M
RAJZBAUM, G
ZHANG, XG
ATTAL, M
RUSALEN, C
WIJDENES, J
MANNONI, P
MARANINCHI, D
PIECHACZYK, M
BATAILLE, R
KLEIN, B
机构
[1] CTR REG TRANSFUS SANGUINE,TOULOUSE,FRANCE
[2] CTR REG TRANSFUS SANGUINE,BESANCON,FRANCE
[3] SERV HEMATOL,MARSEILLE,FRANCE
[4] CTR PAOLI CALMETTES,MARSEILLE,FRANCE
[5] UNIV MONTPELLIER 2,BIOL MOLEC LAB,F-34060 MONTPELLIER,FRANCE
[6] CTR GUI DE CHAULIAC,MONTPELLIER,FRANCE
关键词
D O I
10.1002/eji.1830210727
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Whether interleukin 6 (IL 6) is an autocrine or paracrine myeloma cell growth factor in vivo remains unresolved. To identify which cells are producing IL 6 in vivo, we have studied the IL 6 gene expression in bone marrow mononuclear cells (BMMC) of 19 patients with multiple myeloma (MM) and in peripheral blood mononuclear cells (PBMC) of 9 patients with plasma cell leukemia (PCL). We found that the IL 6 gene was transcribed by BMMC of most patients with MM (79%). Further, IL6 mRNA was not produced by purified myeloma cells from patients with either MM (5 patients) or PCL, but by the bone marrow environment, mainly by monocytes and myeloid cells (CD13+CD15+ cells). For 2 patients with PCL, for whom PBMC and BMMC samples were available, IL 6 mRNA could be detected in BMMC but not in PBMC. Finally, no IL 6 mRNA was detected in five freshly established IL 6-dependent myeloma cell lines. The present data give a clear-cut demonstration of the paracrine origin of IL 6 in vivo in human MM.
引用
收藏
页码:1759 / 1762
页数:4
相关论文
共 19 条
[1]   SERUM LEVELS OF INTERLEUKIN-6, A POTENT MYELOMA CELL-GROWTH FACTOR, AS A REFLECT OF DISEASE SEVERITY IN PLASMA-CELL DYSCRASIAS [J].
BATAILLE, R ;
JOURDAN, M ;
ZHANG, XG ;
KLEIN, B .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (06) :2008-2011
[2]  
BRAKENHOFF JPJ, 1987, J IMMUNOL, V139, P4116
[3]  
DURIE BGM, 1985, BLOOD, V66, P548
[4]   INTERLEUKIN-6 GENE-EXPRESSION IN NORMAL AND NEOPLASTIC-B CELLS [J].
FREEMAN, GJ ;
FREEDMAN, AS ;
RABINOWE, SN ;
SEGIL, JM ;
HOROWITZ, J ;
ROSEN, K ;
WHITMAN, JF ;
NADLER, LM .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (05) :1512-1518
[5]   CHARACTERIZATION OF A NEW IGG-LAMBDA MYELOMA PLASMA-CELL LINE (EJM) - A FURTHER TOOL IN THE INVESTIGATION OF THE BIOLOGY OF MULTIPLE-MYELOMA [J].
HAMILTON, MS ;
BALL, J ;
BROMIDGE, E ;
LOWE, J ;
FRANKLIN, IM .
BRITISH JOURNAL OF HAEMATOLOGY, 1990, 75 (03) :378-384
[6]  
JACKSON N, 1989, CLIN EXP IMMUNOL, V75, P93
[7]  
JOURDAN M, 1990, 6EME REUN INT LANG F, P66
[8]   AUTOCRINE GENERATION AND REQUIREMENT OF BSF-2/IL-6 FOR HUMAN MULTIPLE MYELOMAS [J].
KAWANO, M ;
HIRANO, T ;
MATSUDA, T ;
TAGA, T ;
HORII, Y ;
IWATO, K ;
ASAOKU, H ;
TANG, B ;
TANABE, O ;
TANAKA, H ;
KURAMOTO, A ;
KISHIMOTO, T .
NATURE, 1988, 332 (6159) :83-85
[9]  
Klein B, 1990, Eur Cytokine Netw, V1, P193
[10]  
KLEIN B, 1989, BLOOD, V73, P517