Division of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Pediatr Blood Cancer. 2014 Apr;61(4):618-26. doi: 10.1002/pbc.24801. Epub 2013 Oct 18.
Survival of patients with osteosarcoma lung metastases has not improved in 20 years. We evaluated the efficacy of combining natural killer (NK) cells with aerosol interleukin-2 (IL-2) to achieve organ-specific NK cell migration and expansion in the metastatic organ, and to decrease toxicity associated with systemic IL-2.
Five human osteosarcoma cell lines and 103 patient samples (47 primary and 56 metastatic) were analyzed for NKG2D ligand (NKG2DL) expression. Therapeutic efficacy of aerosol IL-2 + NK cells was evaluated in vivo compared with aerosol IL-2 alone and NK cells without aerosol IL-2.
Osteosarcoma cell lines and patient samples expressed various levels of NKG2DL. NK-mediated killing was NKG2DL-dependent and correlated with expression levels. Aerosol IL-2 increased NK cell numbers in the lung and within metastatic nodules but not in other organs. Therapeutic efficacy, as judged by tumor number, size, and quantification of apoptosis, was also increased compared with NK cells or aerosol IL-2 alone. There were no IL-2-associated systemic toxicities.
Aerosol IL-2 augmented the efficacy of NK cell therapy against osteosarcoma lung metastasis, without inducing systemic toxicity. Our data suggest that lung-targeted IL-2 delivery circumvents toxicities induced by systemic administration. Combining aerosol IL-2 with NK cell infusions, may be a potential new therapeutic approach for patients with osteosarcoma lung metastasis.
20 年来,骨肉瘤肺转移患者的生存率没有提高。我们评估了将自然杀伤 (NK) 细胞与雾化白细胞介素-2 (IL-2) 相结合以实现 NK 细胞在转移器官中的特异性归巢和扩增,并降低与全身 IL-2 相关毒性的疗效。
分析了 5 个人骨肉瘤细胞系和 103 例患者样本(47 例原发和 56 例转移),以评估 NKG2D 配体(NKG2DL)的表达。与单独雾化 IL-2 和没有雾化 IL-2 的 NK 细胞相比,评估了雾化 IL-2+NK 细胞的体内治疗效果。
骨肉瘤细胞系和患者样本表达不同水平的 NKG2DL。NK 介导的杀伤与 NKG2DL 依赖性和表达水平相关。雾化 IL-2 增加了肺和转移性结节内 NK 细胞的数量,但不会增加其他器官的数量。与 NK 细胞或单独雾化 IL-2 相比,疗效(以肿瘤数量、大小和凋亡定量判断)也得到了提高。没有与 IL-2 相关的全身毒性。
雾化 IL-2 增强了 NK 细胞治疗骨肉瘤肺转移的疗效,而没有引起全身毒性。我们的数据表明,靶向肺部的 IL-2 输送可避免全身给药引起的毒性。将雾化 IL-2 与 NK 细胞输注相结合,可能是骨肉瘤肺转移患者的一种潜在新治疗方法。