French R R, Hamblin T J, Bell A J, Tutt A L, Glennie M J
Tenovus Research Laboratory, Southampton General Hospital, UK.
Lancet. 1995 Jul 22;346(8969):223-4. doi: 10.1016/s0140-6736(95)91271-1.
We report the use of a bispecific F(ab')2 antibody to target the ribosome-inactivating protein saporin to the surface antigen CD22 in the treatment of low-grade, end-stage, B-cell lymphoma. Four patients were treated. Toxic effects were minimal (grade I), with mild fever, weakness, and myalgia for 1-2 days after treatment. One patient showed an antibody response to mouse Fab' and saporin. All patients showed rapid and beneficial responses to treatment with improvements in most disease sites and in peripheral blood cytopenia. The responses were short-lived (less than 28 days) but further study of this targeting system is warranted.
我们报告了使用双特异性F(ab')2抗体将核糖体失活蛋白皂草素靶向表面抗原CD22来治疗低度、终末期B细胞淋巴瘤。对4例患者进行了治疗。毒性作用轻微(I级),治疗后1 - 2天出现轻度发热、乏力和肌痛。1例患者对小鼠Fab'和皂草素产生抗体反应。所有患者对治疗均表现出快速且有益的反应,大多数疾病部位及外周血细胞减少情况均有改善。这些反应持续时间较短(少于28天),但该靶向系统值得进一步研究。