Department of Haematology, Derriford Hospital, Plymouth, UK.
Acta Haematol. 2010;123(1):21-9. doi: 10.1159/000257990. Epub 2009 Nov 12.
Thalidomide and lenalidomide are immunomodulatory drugs that show promise in mantle cell lymphoma (MCL). In this study, their potential mechanisms of action against MCL cells were investigated, both alone and in combination with rituximab. Thalidomide, lenalidomide and rituximab have no direct effect on MCL cell viability. However, both immunomodulatory drugs indirectly affect viability by enhancing peripheral blood mononuclear cell-mediated cytotoxicity, with lenalidomide inducing significantly higher levels of toxicity than thalidomide. Rituximab induces both complement-dependent and antibody-dependent cellular cytotoxicity (ADCC) against MCL cells. Rituximab-induced ADCC is enhanced by lenalidomide and, to a lesser extent, thalidomide. Preliminary in vivo findings in MCL patients treated with thalidomide support a role for natural killer cells in the efficacy of these drugs. In conclusion, our data support a role for immunomodulatory drugs in the treatment of MCL.
沙利度胺和来那度胺是免疫调节药物,在套细胞淋巴瘤(MCL)中显示出应用潜力。本研究旨在探究这些药物单独及与利妥昔单抗联合应用时针对 MCL 细胞的潜在作用机制。沙利度胺、来那度胺和利妥昔单抗对 MCL 细胞的活力无直接影响。然而,这两种免疫调节药物均可通过增强外周血单个核细胞介导的细胞毒性间接影响细胞活力,其中来那度胺诱导的毒性水平显著高于沙利度胺。利妥昔单抗诱导针对 MCL 细胞的补体依赖性和抗体依赖性细胞毒性(ADCC)。来那度胺增强利妥昔单抗诱导的 ADCC,而沙利度胺的增强作用较小。沙利度胺治疗 MCL 患者的初步体内研究结果支持自然杀伤细胞在这些药物疗效中的作用。总之,本研究数据支持免疫调节药物在 MCL 治疗中的作用。