Agonist anti-gp130 transducer monoclonal antibodies are human myeloma cell survival and growth factors

被引:51
作者
Gu, ZJ
De Vos, J
Rebouissou, C
Jourdan, M
Zhang, XG
Rossi, JF
Wijdenes, J
Klein, B
机构
[1] INSERM, U475, F-34197 Montpellier 5, France
[2] Inst Mol Genet, Montpellier, France
[3] Hop Lapeyronie, Serv Malad Sang, Montpellier, France
[4] Diaclone, Besancon, France
[5] Hop St Eloi, Unit Cellular Therapy, Montpellier, France
关键词
myeloma; IL-6; gp130; apoptosis; proliferation;
D O I
10.1038/sj.leu.2401632
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have previously reported obtaining two monoclonal antibodies (mAb) against the human gp130 interleukin-6 (IL-6) transducer which made possible the dimerization of gp130 and the activation of several IL-6-driven functions when used together. We report here that these mAb induce gp130-mediated signaling in human myeloma cells and support the survival and the long-term growth of five IL-6-dependent human myeloma cell lines. Their agonist activity is not affected by neutralizing antibodies to IL-6 or IL-6R, These mAb induce a transient proliferation of primary myeloma cells from most patients with multiple myeloma, Again, IL-6 inhibitors do not affect this agonist activity. By using highly purified primary myeloma cells, we found that these anti-gp130 mAb supported the long-term survival of primary myeloma cells from five patients with primary plasma cell leukemia but failed to induce their long-term growth. For patients with fulminant disease and secondary extramedullary proliferation, the antibodies supported a long-term survival and growth, and anti-gp130 mAb-dependent cell lines were obtained. For patients with medullary involvement only, a co-stimulatory signal is necessary, together with gp130 activation, to trigger cell survival and cycling.
引用
收藏
页码:188 / 197
页数:10
相关论文
共 53 条
[1]  
ALEXANIAN R, 1995, SEMIN HEMATOL, V32, P20
[2]   Dimerization and activation of the common transducing chain (gp130) of the cytokines of the IL-6 family by mAb [J].
Autissier, P ;
De Vos, J ;
Liautard, J ;
Tupitsyn, N ;
Jacquet, C ;
Chavdia, N ;
Klein, B ;
Brochier, J ;
Gaillard, JP .
INTERNATIONAL IMMUNOLOGY, 1998, 10 (12) :1881-1889
[3]   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
[4]  
BILLADEAU D, 1995, CANCER RES, V55, P3640
[5]   Long-term bone marrow cultured stromal cells regulate myeloma tumour growth in vitro:: studies with primary tumour cells and LTBMC-dependent cell lines [J].
Bloem, AC ;
Lamme, T ;
de Smet, M ;
Kok, H ;
Vooijs, W ;
Wijdenes, J ;
Boom, SE ;
Lokhorst, HM .
BRITISH JOURNAL OF HAEMATOLOGY, 1998, 100 (01) :166-175
[6]   The biology of replicative senescence [J].
Campisi, J .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (05) :703-709
[7]  
Carey DJ, 1997, BIOCHEM J, V327, P1
[8]   Constitutive activation of Stat3 signaling confers resistance to apoptosis in human U266 myeloma cells [J].
Catlett-Falcone, R ;
Landowski, TH ;
Oshiro, MM ;
Turkson, J ;
Levitzki, A ;
Savino, R ;
Ciliberto, G ;
Moscinski, L ;
Fernández-Luna, JL ;
Nuñez, G ;
Dalton, WS ;
Jove, R .
IMMUNITY, 1999, 10 (01) :105-115
[9]   Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3 [J].
Chesi, M ;
Nardini, E ;
Brents, LA ;
Schrock, E ;
Ried, T ;
Kuehl, WM ;
Bergsagel, PL .
NATURE GENETICS, 1997, 16 (03) :260-264
[10]  
CORRADINI P, 1993, BLOOD, V81, P2708