Immunotherapy of human ovarian carcinoma with OVAREX™ MAb-B43.13 in a human-PBL-SCID/BG mouse model

被引:26
作者
Schultes, BC [1 ]
Zhang, CS [1 ]
Xue, LY [1 ]
Noujaim, AA [1 ]
Madiyalakan, R [1 ]
机构
[1] Univ Alberta, AltraRex Corp, Edmonton, AB T6G 2N8, Canada
来源
HYBRIDOMA | 1999年 / 18卷 / 01期
关键词
D O I
10.1089/hyb.1999.18.47
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The monoclonal antibody (MAb) B43.13, binding to the ovarian cancer-associated antigen CA125, has been injected into more than 200 patients with ovarian cancer to detect recurrence of the disease. The follow-up of the patients revealed surprisingly long survival spans for several patients despite high CA125 levels. To investigate the therapeutic effectiveness of OvaRex(TM) MAb-B43.13 (AltaRex, Edmonton, Canada) under well-controlled conditions, the antibody was tested in a human-PBL-SCID/BG mouse model with CA125 positive human ovarian cancer cells. Mice were reconstituted with human peripheral blood lymphocytes (PBL, normal donors) by intraperitoneal (IP) injection of 2 to 3 x 10(7) PBL/mouse, OvaRex(TM) MAb-B43.13 was administered at 100 mu g/mouse in phosphate buffered saline (PBS), in three different experimental set-ups. An isotype-matched control antibody (MOPC21 or MAb-170) and PBS injection served as controls. The ovarian cancer cell line NIH:OVCAR-NU-3 was injected IP at 1 x 10(6) cells/mouse or subcutaneously (SC) at 4 x 10(6) cells/mouse. Human-PBL-SCID/BG mice were either immunized before injection of tumor cells, along with tumor cells or after small tumors were established (2 weeks after transplantation). Antibody injections were repeated twice in 2-week intervals. Functional and cellular characterization of serum and PBL from these mice demonstrated the successful engraftment of a human immune system in those mice, All three experiments showed that OvaRex(TM) MAb-B43.13 treatment could (a) delay or prevent development of tumors; (b) reduce the size of small established tumors (SC tumor injection) or suppress ascites formation; (c) delay tumor growth when injected prior to tumor implantation; and (d) prolong the survival of the mice (i.p. tumor injection).
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页码:47 / 55
页数:9
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