研究概要
过继性细胞疗法(ACT)为治疗耐药的转移性黑色素瘤患者提供了一种有前景的替代方法。
中文摘要
过继性细胞治疗(ACT)为治疗耐药的转移性黑色素瘤患者提供了一种有前景的替代方法。近年来,与常规化疗或免疫治疗相比,TIL(肿瘤浸润淋巴细胞)治疗和嵌合抗原受体(CAR)-T细胞治疗已显示出改善的临床结局。然而,它们受到肿瘤免疫逃逸、细胞因子释放综合征以及自体治疗制造挑战的限制。相反,自然杀伤(NK)细胞的临床应用已显示出良好的临床安全性特征,毒性极低,提供了一种令人鼓舞的治疗替代方案。与T细胞不同,NK细胞除其他机制外,还可通过HLA I类分子下调而被激活,从而克服肿瘤免疫逃逸的障碍。然而,在黑色素瘤患者中已观察到NK细胞功能受损,导致自然防御能力下降。为克服这一局限,在早期临床试验中已将“激活的”自体或异体NK细胞输注给黑色素瘤患者,显示出令人鼓舞的临床获益。此外,随着多种基于NK细胞的治疗药物正在针对不同癌症进行开发,越来越多旨在增加过继转移NK细胞向实体瘤迁移和浸润的方法正在临床前研究中。这些进展表明,过继性NK细胞治疗未来有望成为转移性黑色素瘤的一种极具前景的治疗方法。
展开英文摘要原文
Adoptive cell therapy (ACT) represents a promising alternative approach for patients with treatment-resistant metastatic melanoma. Lately, tumor infiltrating lymphocyte (TIL) therapy and chimeric antigen receptor (CAR)-T cell therapy have shown improved clinical outcome, compared to conventional chemotherapy or immunotherapy. Nevertheless, they are limited by immune escape of the tumor, cytokine release syndrome, and manufacturing challenges of autologous therapies. Conversely, the clinical use of Natural Killer (NK) cells has demonstrated a favorable clinical safety profile with minimal toxicities, providing an encouraging treatment alternative. Unlike T cells, NK cells are activated, amongst other mechanisms, by the downregulation of HLA class I molecules, thereby overcoming the hurdle of tumor immune escape. However, impairment of NK cell function has been observed in melanoma patients, resulting in deteriorated natural defense. To overcome this limitation, "activated" autologous or allogeneic NK cells have been infused into melanoma patients in early clinical trials, showing encouraging clinical benefit. Furthermore, as several NK cell-based therapeutics are being developed for different cancers, an emerging variety of approaches to increase migration and infiltration of adoptively transferred NK cells towards solid tumors is under preclinical investigation. These developments point to adoptive NK cell therapy as a highly promising treatment for metastatic melanoma in the future.
论文信息
- 作者
- van Vliet AA、Georgoudaki AM、Raimo M、de Gruijl TD、Spanholtz J
- 单位
- Glycostem Therapeutics, Kloosterstraat 9, 5349 AB Oss, The Netherlands.Netherlands
- 文献类型
- 综述
- 期刊
- Cancers2021 Sep 21