Center for Precision Medicine, Department of Medicine, University of Missouri, 1 Hospital Drive, Columbia, MI 65212, USA.
Cells. 2021 Dec 1;10(12):3376. doi: 10.3390/cells10123376.
Acute myeloid leukemia (AML) is a heterogeneous disease associated with various alterations in T cell phenotype and function leading to an abnormal cell population, ultimately leading to immune exhaustion. However, restoration of T cell function allows for the execution of cytotoxic mechanisms against leukemic cells in AML patients. Therefore, long-term disease control, which requires multiple therapeutic approaches, includes those aimed at the re-establishment of cytotoxic T cell activity. AML treatments that harness the power of T lymphocytes against tumor cells have rapidly evolved over the last 3 to 5 years through various stages of preclinical and clinical development. These include tissue-infiltrated lymphocytes (TILs), bispecific antibodies, immune checkpoint inhibitors (ICIs), chimeric antigen receptor T (CAR-T) cell therapy, and tumor-specific T cell receptor gene-transduced T (TCR-T) cells. In this review, these T cell-based immunotherapies and the potential of TILs as a novel antileukemic therapy will be discussed.
急性髓系白血病(AML)是一种异质性疾病,与 T 细胞表型和功能的各种改变相关,导致异常细胞群的出现,最终导致免疫衰竭。然而,T 细胞功能的恢复可以使 AML 患者的细胞毒性机制针对白血病细胞发挥作用。因此,需要多种治疗方法的长期疾病控制,包括旨在重新建立细胞毒性 T 细胞活性的方法。在过去的 3 到 5 年中,通过临床前和临床开发的各个阶段,利用 T 淋巴细胞对抗肿瘤细胞的力量的 AML 治疗方法迅速发展。这些方法包括组织浸润淋巴细胞(TILs)、双特异性抗体、免疫检查点抑制剂(ICI)、嵌合抗原受体 T(CAR-T)细胞疗法和肿瘤特异性 T 细胞受体基因转导的 T(TCR-T)细胞。在这篇综述中,将讨论这些基于 T 细胞的免疫疗法以及 TILs 作为一种新型抗白血病疗法的潜力。