José Carreras Center for Immuno and Gene Therapy, Saarland University, Homburg, Saarland, Germany.
Department of Internal Medicine I, Saarland University Medical Center, Kirrberger Strasse 100, 66421, Homburg, Saarland, Germany.
Cancer Immunol Immunother. 2018 Nov;67(11):1709-1718. doi: 10.1007/s00262-018-2224-y. Epub 2018 Aug 21.
Vitamin D3 (25-OH-D3) deficiency impairs rituximab-dependent cellular cytotoxicity and the outcome of patients with diffuse large B-cell and follicular lymphomas (DLBCL). Since the optimum 25-OH-D3 serum levels for NK cell-mediated antibody-dependent cellular cytotoxicity (ADCC) are unknown, we determined the 25-OH-D3 serum levels associated with maximum NK cell-mediated ADCC. CD20 antibody-loaded CD20 B-cell lymphoma cell lines were cultured with NK cells and ADCC activity was determined by lactate dehydrogenase release assays. Using a newly developed formula, pre-defined 25-OH-D3 serum levels were achieved with high individual precision over a wide range. NK cells from 20 healthy individuals killed antibody-treated CD20 lymphoma cells in a concentration- and E:T ratio-dependent manner with obinutuzumab displaying a stronger ADCC activity than rituximab. Maximum NK-cell activity and ADCC were observed at 65 ng/ml 25-OH-D3, the middle of the normal range (30-100 ng/ml). 25-OH-D3 serum levels around this range should be the target in interventional trials aiming at improving NK cell-mediated ADCC by 25-OH-D3 substitution. Lower levels do not provide significant ADCC improvements in individuals with 25-OH-D3 deficiency or insufficiency and might result in the failure of interventions with 25-OH-D3.
维生素 D3(25-OH-D3)缺乏会损害利妥昔单抗依赖性细胞毒性和弥漫性大 B 细胞淋巴瘤和滤泡性淋巴瘤(DLBCL)患者的预后。由于 NK 细胞介导的抗体依赖性细胞毒性(ADCC)的最佳 25-OH-D3 血清水平尚不清楚,我们确定了与最大 NK 细胞介导的 ADCC 相关的 25-OH-D3 血清水平。用 NK 细胞培养载有 CD20 抗体的 CD20 B 细胞淋巴瘤细胞系,并通过乳酸脱氢酶释放测定法测定 ADCC 活性。使用新开发的公式,在广泛的范围内以高个体精度实现了预先定义的 25-OH-D3 血清水平。来自 20 名健康个体的 NK 细胞以浓度和 E:T 比依赖性方式杀死抗体处理的 CD20 淋巴瘤细胞,奥滨尤妥珠单抗比利妥昔单抗显示出更强的 ADCC 活性。在 25-OH-D3 为 65ng/ml 的情况下观察到最大的 NK 细胞活性和 ADCC,这处于正常范围(30-100ng/ml)的中间。在干预试验中,应将该范围内的 25-OH-D3 血清水平作为目标,旨在通过 25-OH-D3 替代来提高 NK 细胞介导的 ADCC。在 25-OH-D3 缺乏或不足的个体中,较低的水平不会提供显著的 ADCC 改善,并且可能导致 25-OH-D3 干预失败。