Cecilia Restelli, Marco Ruella, Luca Paruzzo, Corrado Tarella, Pier Giuseppe Pelicci, Emanuela Colombo
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引用次数: 0
摘要
尽管急性髓性白血病(AML)的治疗取得了进展,但目前的疗法仍无法征服它。急性髓性白血病发展过程中的免疫逃避证据(如 HLA 丢失和 T 细胞衰竭)表明,抗白血病免疫反应有助于疾病控制,可以通过免疫疗法加以利用。在这篇综述中,我们将讨论一系列急性髓细胞性白血病免疫疗法靶点,包括癌细胞内在抗原和表面抗原以及白血病环境中的靶点,以及如何为个性化方法量身定制这些靶点。这些靶点概述了应用于急性髓细胞白血病的主要免疫疗法模式:免疫检查点抑制剂、抗体药物共轭物、治疗性疫苗、双特异性/三特异性抗体以及嵌合抗原受体(CAR)-T 和 CAR-NK 细胞。意义重大:治疗急性髓细胞性白血病的免疫疗法显示出不断发展的前景。正在进行的研究旨在针对不同的患者特征和临床情况定制治疗方法。本综述涵盖免疫监视机制、检查点抑制剂、抗体、CAR-T/NK 细胞和疫苗等治疗方案,以及耐药机制和微环境因素。
Recent Advances in Immune-Based Therapies for Acute Myeloid Leukemia.
Despite advancements, acute myeloid leukemia (AML) remains unconquered by current therapies. Evidence of immune evasion during AML progression, such as HLA loss and T-cell exhaustion, suggests that antileukemic immune responses contribute to disease control and could be harnessed by immunotherapy. In this review, we discuss a spectrum of AML immunotherapy targets, encompassing cancer cell-intrinsic and surface antigens as well as targeting in the leukemic milieu, and how they can be tailored for personalized approaches. These targets are overviewed across major immunotherapy modalities applied to AML: immune checkpoint inhibitors, antibody-drug conjugates, therapeutic vaccines, bispecific/trispecific antibodies, and chimeric antigen receptor (CAR)-T and CAR-NK cells. Significance: Immune therapies in AML treatment show evolving promise. Ongoing research aims to customize approaches for varied patient profiles and clinical scenarios. This review covers immune surveillance mechanisms, therapy options like checkpoint inhibitors, antibodies, CAR-T/NK cells, and vaccines, as well as resistance mechanisms and microenvironment considerations.
期刊介绍:
The journal Blood Cancer Discovery publishes high-quality Research Articles and Briefs that focus on major advances in basic, translational, and clinical research of leukemia, lymphoma, myeloma, and associated diseases. The topics covered include molecular and cellular features of pathogenesis, therapy response and relapse, transcriptional circuits, stem cells, differentiation, microenvironment, metabolism, immunity, mutagenesis, and clonal evolution. These subjects are investigated in both animal disease models and high-dimensional clinical data landscapes.
The journal also welcomes submissions on new pharmacological, biological, and living cell therapies, as well as new diagnostic tools. They are interested in prognostic, diagnostic, and pharmacodynamic biomarkers, and computational and machine learning approaches to personalized medicine. The scope of submissions ranges from preclinical proof of concept to clinical trials and real-world evidence.
Blood Cancer Discovery serves as a forum for diverse ideas that shape future research directions in hematooncology. In addition to Research Articles and Briefs, the journal also publishes Reviews, Perspectives, and Commentaries on topics of broad interest in the field.