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嵌合抗原受体(CAR)T细胞疗法治疗急性髓系白血病(AML)。

Chimeric Antigen Receptor (CAR) T Cell Therapy in Acute Myeloid Leukemia (AML).

作者信息

Hofmann Susanne, Schubert Maria-Luisa, Wang Lei, He Bailin, Neuber Brigitte, Dreger Peter, Müller-Tidow Carsten, Schmitt Michael

机构信息

Department of Internal Medicine V (Hematology/Oncology/Rheumatology), University Hospital Heidelberg, 69120 Heidelberg, Germany.

National Center for Tumor Diseases (NCT), 69120 Heidelberg, Germany.

出版信息

J Clin Med. 2019 Feb 6;8(2):200. doi: 10.3390/jcm8020200.

Abstract

Despite high response rates after initial chemotherapy in patients with acute myeloid leukemia (AML), relapses occur frequently, resulting in a five-year-survival by <30% of the patients. Hitherto, allogeneic hemotopoietic stem cell transplantation (allo-HSCT) is the best curative treatment option in intermediate and high risk AML. It is the proof-of-concept for T cell-based immunotherapies in AML based on the graft-versus-leukemia (GvL)-effect, but it also bears the risk of graft-versus-host disease. CD19-targeting therapies employing chimeric antigen receptor (CAR) T cells are a breakthrough in cancer therapy. A similar approach for myeloid malignancies is highly desirable. This article gives an overview on the state-of-the art of preclinical and clinical studies on suitable target antigens for CAR T cell therapy in AML patients.

摘要

尽管急性髓系白血病(AML)患者在初始化疗后缓解率较高,但复发频繁,导致患者五年生存率低于30%。迄今为止,异基因造血干细胞移植(allo-HSCT)是中高危AML患者最佳的根治性治疗选择。基于移植物抗白血病(GvL)效应,它是AML中基于T细胞的免疫疗法的概念验证,但也存在移植物抗宿主病的风险。采用嵌合抗原受体(CAR)T细胞的CD19靶向疗法是癌症治疗的一项突破。对于髓系恶性肿瘤,类似的方法非常可取。本文概述了AML患者CAR T细胞治疗合适靶抗原的临床前和临床研究现状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16b6/6406805/391af88ef142/jcm-08-00200-g001.jpg

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