Khan Ghazala Naz, Orchard Kim, Guinn Barbara-Ann
Department of Biomedical Sciences, University of Hull, Hull HU7 6RX, UK.
Department of Haematology, University Hospital Southampton NHS Foundation Trust, Southampton SO16 6YD, UK.
J Clin Med. 2019 Jan 23;8(2):134. doi: 10.3390/jcm8020134.
One of the most promising approaches to preventing relapse is the stimulation of the body's own immune system to kill residual cancer cells after conventional therapy has destroyed the bulk of the tumour. In acute myeloid leukaemia (AML), the high frequency with which patients achieve first remission, and the diffuse nature of the disease throughout the periphery, makes immunotherapy particularly appealing following induction and consolidation therapy, using chemotherapy, and where possible stem cell transplantation. Immunotherapy could be used to remove residual disease, including leukaemic stem cells from the farthest recesses of the body, reducing, if not eliminating, the prospect of relapse. The identification of novel antigens that exist at disease presentation and can act as targets for immunotherapy have also proved useful in helping us to gain a better understand of the biology that belies AML. It appears that there is an additional function of leukaemia associated antigens as biomarkers of disease state and survival. Here, we discuss these findings.
预防复发最有前景的方法之一是在传统疗法摧毁大部分肿瘤后,刺激机体自身免疫系统来杀死残留的癌细胞。在急性髓系白血病(AML)中,患者首次缓解的高频率以及疾病在全身外周的弥漫性,使得免疫疗法在诱导和巩固治疗(使用化疗,并尽可能进行干细胞移植)后显得格外有吸引力。免疫疗法可用于清除残留疾病,包括来自身体最隐蔽部位的白血病干细胞,即便不能消除复发的可能性,也能降低其复发几率。已证明,识别疾病初发时存在且可作为免疫治疗靶点的新抗原,有助于我们更好地理解AML背后的生物学机制。白血病相关抗原似乎还具有作为疾病状态和生存生物标志物的额外功能。在此,我们讨论这些发现。