The human anti-CD30 antibody 5F11 shows in vitro and in vivo activity against malignant lymphoma

被引:73
作者
Borchmann, P
Treml, JF
Hansen, H
Gottstein, C
Schnell, R
Staak, O
Zhang, HF
Davis, T
Keler, T
Diehl, V
Graziano, RF
Engert, A
机构
[1] Univ Cologne, Innere Med Klin 1, D-50924 Cologne, Germany
[2] Medarex Inc, Bloomsbury, NJ USA
关键词
D O I
10.1182/blood-2003-02-0515
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CD30 is a promising target for antibody-based immunotherapy of Hodgkin lymphoma (HL) and anaplastic large cell lymphoma. To overcome the limitations from currently available murine anti-CD30 monoclonal antibodies (mAbs), a new fully human anti-CD30 antibody was generated. Binding properties were evaluated by recombinant CD30 capture enzyme-linked immunosorbent assay (ELISA) and fluorescence-activated cell-sorter (FACS) flow cytometry. Activity of this new mAb was assessed in vitro using growth inhibition and anti body-dependent cellular cytotoxicity (ADCC) assays on several cell lines. In vivo activity was determined in a solid as well as in a disseminated xenografted model of HL in severe combined immunodeficiency (SCID) mice. The mAb 5F11 showed specific binding to CD30 (cluster A). The ADCC assays indicated dose-dependent lysis of L540 cells when 5F11 was combined with human effector cells. Upon cross-linking in vitro, 5F11 inhibited the growth of CD30-expressing cell lines. In vivo, treatment with 5F11 induced a marked growth delay or even a complete regression of established xenografted HL in SCID mice. In the disseminated HL model, a high proportion of 5F11-treated mice experienced long-term survival. The new human anti-CD30 monoclonal antibody 5F11 shows promise as a means of CD30-targeted immunotherapy of malignant lymphomas. Based on these results, a clinical phase 1 study in patients with refractory CD30(+) lymphoma has been initiated. (C) 2003 by The American Society of Hematology.
引用
收藏
页码:3737 / 3742
页数:6
相关论文
共 37 条
[1]  
BONADONNA G, 1982, CANCER TREAT REP, V66, P881
[2]   INDICATIONS FOR AUTOLOGOUS BONE-MARROW TRANSPLANTATION IN HODGKINS-DISEASE [J].
CARELLA, AM .
LEUKEMIA & LYMPHOMA, 1992, 7 :21-22
[3]   CD30 in normal and neoplastic cells [J].
Chiarle, R ;
Podda, A ;
Prolla, G ;
Gong, J ;
Thorbecke, GJ ;
Inghirami, G .
CLINICAL IMMUNOLOGY, 1999, 90 (02) :157-164
[4]  
Chiarle R, 1999, J IMMUNOL, V163, P194
[5]   CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma. [J].
Coiffier, B ;
Lepage, E ;
Brière, J ;
Herbrecht, R ;
Tilly, H ;
Bouabdallah, R ;
Morel, P ;
Van den Neste, E ;
Salles, G ;
Gaulard, P ;
Reyes, F ;
Gisselbrecht, C .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (04) :235-242
[6]   COMBINATION CHEMOTHERAPY IN TREATMENT OF ADVANCED HODGKINS DISEASE [J].
DEVITA, VT ;
SERPICK, AA ;
CARBONE, PP .
ANNALS OF INTERNAL MEDICINE, 1970, 73 (06) :881-+
[7]   BEACOPP, a new dose-escalated and accelerated regimen, is at least as effective as COPP/ABVD in patients with advanced-stage Hodgkin's lymphoma: Interim report from a trial of the German Hodgkin's Lymphoma Study Group [J].
Diehl, V ;
Franklin, J ;
Hasenclever, D ;
Tesch, H ;
Pfreundschuh, M ;
Lathan, B ;
Paulus, U ;
Sieber, M ;
Rueffer, JU ;
Sextro, M ;
Engert, A ;
Wolf, J ;
Hermann, R ;
Holmer, L ;
Stappert-Jahn, U ;
Winnerlein-Trump, E ;
Wulf, G ;
Krause, S ;
Glunz, A ;
von Kalle, K ;
Bischoff, H ;
Haedicke, C ;
Duehmke, E ;
Georgii, A ;
Loeffler, M .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (12) :3810-3821
[8]  
ENGERT A, 1990, CANCER RES, V50, P84
[9]   INVIVO TARGETING OF HODGKIN AND REED-STERNBERG CELLS OF HODGKINS-DISEASE WITH MONOCLONAL-ANTIBODY BER-H2 (CD30) - IMMUNOHISTOLOGICAL EVIDENCE [J].
FALINI, B ;
FLENGHI, L ;
FEDELI, L ;
BROE, MK ;
BONINO, C ;
STEIN, H ;
DURKOP, H ;
BIGERNA, B ;
BARBABIETOLA, G ;
VENTURI, S ;
AVERSA, F ;
PIZZOLO, G ;
BARTOLI, A ;
PILERI, S ;
SABATTINI, E ;
PALUMBO, R ;
MARTELLI, MF .
BRITISH JOURNAL OF HAEMATOLOGY, 1992, 82 (01) :38-45
[10]   Characterization of the CD30L binding domain on the human CD30 molecule using anti-CD30 antibodies [J].
Franke, AC ;
Jung, D ;
Ellis, TM .
HYBRIDOMA, 2000, 19 (01) :43-48