Tavakoli Shirin, Samareh-Salavatipour Maryam, Mardi Amirhossein, Salehi-Shadkami Hossein, Vaezi Mohammad, Barkhordar Maryam, Ahmadvand Mohammad
Department of Applied Cell Sciences, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Discov Oncol. 2025 May 8;16(1):694. doi: 10.1007/s12672-025-02489-0.
Lymphoma, a cancer with poor prognosis is a growing global health challenge that encompasses two primary types, Hodgkin (HL) and non-Hodgkin lymphoma (NHL), each further divided into various subtypes with distinct biological behaviors. Conventional therapeutic strategies include chemotherapy, radiation, surgery, and autologous hematopoietic stem cell transplantation (auto-HSCT). Natural killer (NK) cells exhibit intrinsic cytotoxicity against tumor cells without the need for prior immunization or activation. In this prospective clinical trial, we evaluated the feasibility of allogeneic NK cell therapy in patients with high-risk lymphoma who had a poor prognosis. Each patient received 1 × 107 NK cells/kg infusion without interleukin-2 (IL-2) supplementation. Therapy was tolerated without graft-versus-host-disease, cytokine release syndrome, or neurotoxicity. During the follow-up period, 7 had complete responses (CR) (87.5%) and one case exhibited stable disease (SD) (12.5%). In summary, our investigations support the development of allogeneic NK cellular therapies for advanced lymphoma to overcome chemoresistance. Therapeutic efficacy may be further improved by disrupting the immunosuppressive environment and infusion of exogenous IL-15. This approach presents a promising and pragmatic strategy for managing high-risk lymphoma post-HSCT. Future research should focus on optimizing NK cell dosages and infusion frequency to maximize treatment effectiveness.
淋巴瘤是一种预后较差的癌症,是一个日益严峻的全球健康挑战,它包括两种主要类型,霍奇金淋巴瘤(HL)和非霍奇金淋巴瘤(NHL),每种类型又进一步分为具有不同生物学行为的各种亚型。传统的治疗策略包括化疗、放疗、手术和自体造血干细胞移植(auto-HSCT)。自然杀伤(NK)细胞对肿瘤细胞具有内在的细胞毒性,无需预先免疫或激活。在这项前瞻性临床试验中,我们评估了异基因NK细胞疗法对预后不良的高危淋巴瘤患者的可行性。每位患者接受1×10⁷ NK细胞/kg输注,不补充白细胞介素-2(IL-2)。治疗耐受性良好,未出现移植物抗宿主病、细胞因子释放综合征或神经毒性。在随访期间,7例患者完全缓解(CR)(87.5%),1例病情稳定(SD)(12.5%)。总之,我们的研究支持开发用于晚期淋巴瘤的异基因NK细胞疗法以克服化疗耐药性。通过破坏免疫抑制环境和输注外源性IL-15,治疗效果可能会进一步提高。这种方法为HSCT后高危淋巴瘤的管理提供了一种有前景且实用的策略。未来的研究应专注于优化NK细胞剂量和输注频率,以最大限度地提高治疗效果。