首页> 美国卫生研究院文献>Italian Journal of Pediatrics >New advances in leukaemia immunotherapy by the use of Chimeric Artificial Antigen Receptors (CARs): state of the art and perspectives for the near future
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New advances in leukaemia immunotherapy by the use of Chimeric Artificial Antigen Receptors (CARs): state of the art and perspectives for the near future

机译:嵌合人工抗原受体(CAR)在白血病免疫治疗中的新进展:最新技术和对近期的展望

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摘要

Leukaemia immunotherapy represents a fascinating and promising field of translational research, particularly as an integrative approach of bone marrow transplantation. Adoptive immunotherapy by the use of donor-derived expanded leukaemia-specific T cells has showed some kind of clinical response, but the major advance is nowadays represented by gene manipulation of donor immune cells, so that they acquire strict specificity towards the tumour target and potent lytic activity, followed by significant proliferation, increased survival and possibly anti-tumour memory state. This is achieved by gene insertion of Chimeric T-cell Antigen Receptors (CARs), which are artificial molecules containing antibody-derived fragments (to bind the specific target), joined with potent signalling T-Cell Receptor (TCR)-derived domains that activate the manipulated cells. This review will discuss the main application of this approach particularly focusing on the paediatric setting, raising advantages and disadvantages and discussing relevant perspectives of use in the nearest future.
机译:白血病免疫疗法代表了一个引人入胜且充满希望的转化研究领域,尤其是作为骨髓移植的一种综合方法。通过使用供体来源的扩增的白血病特异性T细胞进行的过继免疫疗法已显示出某种临床反应,但如今的主要进展是以供体免疫细胞的基因操作为代表,从而使它们对肿瘤靶标具有严格的特异性并具有强大的治疗作用。裂解活性,继之以明显的增殖,增加的存活率以及可能的抗肿瘤记忆状态。这是通过嵌合T细胞抗原受体(CAR)的基因插入来实现的,嵌合T细胞抗原受体是包含抗体衍生片段(结合特定靶标)的人工分子,并与有效激活T细胞受体(TCR)的结构域连接被操纵的细胞。这篇综述将讨论这种方法的主要应用,特别是着重于儿科环境,提出利弊,并讨论在不久的将来使用的相关观点。

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