Siegel Abby B, Goldenberg David M, Cesano Alessandra, Coleman Morton, Leonard John P
Center for Lymphoma and Myeloma, Weill Medical College of Cornell University, New York, NY, USA.
Semin Oncol. 2003 Aug;30(4):457-64. doi: 10.1016/s0093-7754(03)00240-9.
Immunotherapy directed against the CD20 antigen has had a profound impact on the management of patients with B-cell non-Hodgkin's lymphoma (NHL). Antibody-based treatments offer a favorable side effect profile, as well as alternate mechanisms of action that may complement those of cytotoxic modalities. Targeting other antigens, such as CD22, may also result in antilymphoma effects. This B-cell-specific molecule is widely expressed in NHL and mediates important functions in B-cell biology. Preclinical and early clinical data suggest that epratuzumab, a humanized anti-CD22 monoclonal antibody, demonstrates antilymphoma effects in both unlabeled and radiolabeled forms, as well as a favorable safety profile. Ongoing and future studies will further determine the role of epratuzumab among the array of antilymphoma therapies, both as a single agent and in combination with other agents.
针对CD20抗原的免疫疗法对B细胞非霍奇金淋巴瘤(NHL)患者的治疗产生了深远影响。基于抗体的治疗具有良好的副作用特征,以及可能补充细胞毒性疗法作用机制的其他作用机制。靶向其他抗原,如CD22,也可能产生抗淋巴瘤作用。这种B细胞特异性分子在NHL中广泛表达,并在B细胞生物学中发挥重要功能。临床前和早期临床数据表明,人源化抗CD22单克隆抗体依帕珠单抗以未标记和放射性标记形式均显示出抗淋巴瘤作用,且安全性良好。正在进行的和未来的研究将进一步确定依帕珠单抗在一系列抗淋巴瘤治疗中的作用,无论是作为单一药物还是与其他药物联合使用。