Tong Alexander A, Hashem Hasan, Eid Saada, Allen Frederick, Kingsley Daniel, Huang Alex Y
Department of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Division of Pediatric Hematology-Oncology, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Oncoimmunology. 2017 Mar 16;6(4):e1303586. doi: 10.1080/2162402X.2017.1303586. eCollection 2017.
The survival of patients with metastatic or relapsed Ewing sarcoma (ES) remains dismal despite intensification of combination chemotherapy and radiotherapy, precipitating the need for novel alternative therapies with minimal side effects. Natural killer (NK) cells are promising additions to the field of cellular immunotherapy. Adoptive NK cell therapy has shown encouraging results in hematological malignancies. Despite these initial promising successes, however, NK cell therapy for solid tumors remains to be investigated using tumor models. The purpose of this study is to evaluate the efficacy of expanded human NK cells in controlling primary and metastatic ES tumor growth and Using membrane-bound IL-21 containing K562 (K562-mbIL-21) expansion platform, we were able to obtain sufficient numbers of expanded NK (eNK) cells that display favorable activation phenotypes and inflammatory cytokine secretion, along with a strong cytotoxic effect against ES. Furthermore, eNK therapy significantly decreased lung metastasis without any significant therapeutic effect in limiting primary tumor growth in an xenograft model. Our data demonstrate that eNK may be effective against pulmonary metastatic ES, but challenges remain to direct proper trafficking and augmenting the cytotoxic function of eNK to target primary tumor sites.
尽管联合化疗和放疗不断强化,但转移性或复发性尤因肉瘤(ES)患者的生存率仍然很低,因此需要副作用最小的新型替代疗法。自然杀伤(NK)细胞是细胞免疫治疗领域很有前景的补充。过继性NK细胞疗法在血液系统恶性肿瘤中已显示出令人鼓舞的结果。然而,尽管取得了这些初步的成功,但实体瘤的NK细胞疗法仍有待通过肿瘤模型进行研究。本研究的目的是评估扩增的人NK细胞在控制原发性和转移性ES肿瘤生长方面的疗效。使用含有膜结合IL-21的K562(K562-mbIL-21)扩增平台,我们能够获得足够数量的扩增NK(eNK)细胞,这些细胞表现出良好的激活表型和炎性细胞因子分泌,同时对ES具有强大的细胞毒性作用。此外,在异种移植模型中,eNK疗法显著减少了肺转移,但在限制原发性肿瘤生长方面没有任何显著的治疗效果。我们的数据表明,eNK可能对肺转移性ES有效,但在引导eNK正确归巢并增强其对原发性肿瘤部位的细胞毒性功能方面仍存在挑战。