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急性白血病的过继性免疫疗法:嵌合抗原受体的新见解

Adoptive immunotherapy for acute leukemia: New insights in chimeric antigen receptors.

作者信息

Heiblig Maël, Elhamri Mohamed, Michallet Mauricette, Thomas Xavier

机构信息

Maël Heiblig, Mohamed Elhamri, Mauricette Michallet, Xavier Thomas, Hematology Department, Lyon-Sud Hospital, 69495 Pierre Bénite cedex, France.

出版信息

World J Stem Cells. 2015 Aug 26;7(7):1022-38. doi: 10.4252/wjsc.v7.i7.1022.

Abstract

Relapses remain a major concern in acute leukemia. It is well known that leukemia stem cells (LSCs) hide in hematopoietic niches and escape to the immune system surveillance through the outgrowth of poorly immunogenic tumor-cell variants and the suppression of the active immune response. Despite the introduction of new reagents and new therapeutic approaches, no treatment strategies have been able to definitively eradicate LSCs. However, recent adoptive immunotherapy in cancer is expected to revolutionize our way to fight against this disease, by redirecting the immune system in order to eliminate relapse issues. Initially described at the onset of the 90's, chimeric antigen receptors (CARs) are recombinant receptors transferred in various T cell subsets, providing specific antigens binding in a non-major histocompatibility complex restricted manner, and effective on a large variety of human leukocyte antigen-divers cell populations. Once transferred, engineered T cells act like an expanding "living drug" specifically targeting the tumor-associated antigen, and ensure long-term anti-tumor memory. Over the last decades, substantial improvements have been made in CARs design. CAR T cells have finally reached the clinical practice and first clinical trials have shown promising results. In acute lymphoblastic leukemia, high rate of complete and prolonged clinical responses have been observed after anti-CD19 CAR T cell therapy, with specific but manageable adverse events. In this review, our goal was to describe CAR structures and functions, and to summarize recent data regarding pre-clinical studies and clinical trials in acute leukemia.

摘要

复发仍然是急性白血病的一个主要问题。众所周知,白血病干细胞(LSCs)隐藏在造血龛中,并通过低免疫原性肿瘤细胞变体的生长和主动免疫反应的抑制来逃避免疫系统的监视。尽管引入了新的试剂和新的治疗方法,但尚无治疗策略能够彻底根除白血病干细胞。然而,最近癌症的过继性免疫疗法有望彻底改变我们对抗这种疾病的方式,即通过重新定向免疫系统来消除复发问题。嵌合抗原受体(CARs)最初在90年代初被描述,是在各种T细胞亚群中转移的重组受体,以非主要组织相容性复合体限制的方式提供特异性抗原结合,并且对多种人类白细胞抗原多样化的细胞群体有效。一旦转移,工程化T细胞就像一种不断扩增的“活药物”,特异性靶向肿瘤相关抗原,并确保长期的抗肿瘤记忆。在过去几十年中,CARs的设计有了实质性的改进。CAR T细胞最终进入了临床实践,首次临床试验已显示出有希望的结果。在急性淋巴细胞白血病中,抗CD19 CAR T细胞治疗后观察到高比例的完全且持久的临床反应,伴有特定但可控制的不良事件。在本综述中,我们的目标是描述CAR的结构和功能,并总结有关急性白血病临床前研究和临床试验的最新数据。

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