Borchmann Peter, Treml John F, Hansen Hinrich, Gottstein Claudia, Schnell Roland, Staak Oliver, Zhang Hui-fen, Davis Thomas, Keler Tibor, Diehl Volker, Graziano Robert F, Engert Andreas
Klinik I für Innere Medizin der Universität Köln, Joseph-Stelzmann Strasse 9, 50924 Cologne, Germany.
Blood. 2003 Nov 15;102(10):3737-42. doi: 10.1182/blood-2003-02-0515. Epub 2003 Jul 24.
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 antibody-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.
CD30是霍奇金淋巴瘤(HL)和间变性大细胞淋巴瘤基于抗体的免疫疗法的一个有前景的靶点。为了克服现有鼠抗CD30单克隆抗体(mAb)的局限性,研发了一种新型全人源抗CD30抗体。通过重组CD30捕获酶联免疫吸附测定(ELISA)和荧光激活细胞分选仪(FACS)流式细胞术评估结合特性。使用几种细胞系的生长抑制和抗体依赖性细胞毒性(ADCC)测定在体外评估这种新型mAb的活性。在严重联合免疫缺陷(SCID)小鼠的HL实体瘤和播散性异种移植模型中测定体内活性。mAb 5F11显示出与CD30(A簇)的特异性结合。ADCC测定表明,当5F11与人效应细胞联合使用时,对L540细胞有剂量依赖性裂解作用。在体外交联后,5F11抑制表达CD30的细胞系的生长。在体内,用5F11治疗可使SCID小鼠中已建立的异种移植HL出现明显的生长延迟甚至完全消退。在播散性HL模型中,高比例接受5F11治疗的小鼠实现了长期存活。新型人抗CD30单克隆抗体5F11有望成为恶性淋巴瘤CD30靶向免疫治疗的一种手段。基于这些结果,已启动了一项针对难治性CD30+淋巴瘤患者的1期临床研究。