Department of Hematology, Oncology and Clinical Immunology, Heinrich-Heine-University, Düsseldorf, Germany.
Cancer Immunol Immunother. 2012 Oct;61(10):1869-75. doi: 10.1007/s00262-012-1339-9. Epub 2012 Sep 14.
Bispecific tetravalent antibodies (TandAb) directed against the B cell surface marker CD19 and activating receptors on T or NK cells (CD19 × CD3 or CD19 × CD16) have shown promising effects in vitro and in preclinical studies. Here, we examine the cytotoxic efficacy of T and NK cells from patients with B cell Non-Hodgkin's Lymphoma (NHL) against B-lymphoma cells following the binding of the matching TandAb. The addition of CD19 × CD16 TandAb led to a threefold increase in NK cell activation in the presence of B-lymphoma cells. Similarly, T cells displayed a sevenfold increase in cytotoxic activity after the addition of CD19 × CD3 TandAb. Comparison of T and NK cell effector function of patients and healthy controls showed comparable levels of cytotoxic activity in response to lymphoma cells and no reduction in functional activity due to age, disease stage or the type and amount of previous therapy. Thus, T and NK cells of patients with B cell NHL are fully capable of being activated by therapeutic crosslinking antibodies. These results provide a rationale for the use of TandAbs for patients with B cell NHL, particularly in cases where remission with minimal residual disease could be achieved by cytotoxic chemotherapy.
双特异性四价抗体(TandAb)针对 B 细胞表面标志物 CD19 和 T 或 NK 细胞上的激活受体(CD19×CD3 或 CD19×CD16),在体外和临床前研究中显示出有希望的效果。在这里,我们研究了源自 B 细胞非霍奇金淋巴瘤(NHL)患者的 T 和 NK 细胞在结合匹配的 TandAb 后对 B 淋巴瘤细胞的细胞毒性功效。在存在 B 淋巴瘤细胞的情况下,添加 CD19×CD16 TandAb 导致 NK 细胞激活增加了三倍。同样,添加 CD19×CD3 TandAb 后,T 细胞的细胞毒性活性增加了七倍。比较患者和健康对照者的 T 和 NK 细胞效应功能表明,对淋巴瘤细胞的细胞毒性活性水平相当,并且由于年龄、疾病阶段或先前治疗的类型和数量,功能活性没有降低。因此,B 细胞 NHL 患者的 T 和 NK 细胞完全能够被治疗性交联抗体激活。这些结果为 B 细胞 NHL 患者使用 TandAb 提供了依据,特别是在通过细胞毒性化疗可以达到最小残留疾病缓解的情况下。