Chandra Daniel J, Alber Bernhard, Saultz Jennifer N
Division of Hematology/Medical Oncology, Oregon Health & Science University, Portland, OR 97239, USA.
Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97239, USA.
Cancers (Basel). 2024 Jul 23;16(15):2615. doi: 10.3390/cancers16152615.
Acute myeloid leukemia (AML) is a complex hematopoietic clonal disorder with limited curative options beyond stem cell transplantation. The success of transplant is intimately linked with the graft versus leukemia effect from the alloreactive donor immune cells including, T and NK cells. The immune system plays a dynamic role in leukemia survival and resistance. Despite our growing understanding of the immune microenvironment, responses to immune-based therapies differ greatly between patients. Herein, we review the biology of immune evasion mechanisms in AML, discuss the current landscape of immunotherapeutic strategies, and discuss the implications of therapeutic targets. This review focuses on T and NK cell-based therapy, including modified and non-modified NK cells, CAR-T and CAR-NK cells, antibodies, and checkpoint blockades. Understanding the complex interchange between immune tolerance and the emergence of tumor resistance will improve patient outcomes.
急性髓系白血病(AML)是一种复杂的造血克隆性疾病,除干细胞移植外,治疗选择有限。移植的成功与来自同种异体反应性供体免疫细胞(包括T细胞和NK细胞)的移植物抗白血病效应密切相关。免疫系统在白血病的存活和耐药中起着动态作用。尽管我们对免疫微环境的了解日益深入,但患者对基于免疫的治疗反应差异很大。在此,我们综述AML免疫逃逸机制的生物学,讨论免疫治疗策略的现状,并探讨治疗靶点的意义。本综述重点关注基于T细胞和NK细胞的治疗,包括修饰和未修饰的NK细胞、CAR-T和CAR-NK细胞、抗体以及检查点阻断。了解免疫耐受与肿瘤耐药性出现之间的复杂相互作用将改善患者预后。