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用于治疗B系淋巴瘤的适配体嵌合抗原受体T细胞疗法

Adapter CAR T Cell Therapy for the Treatment of B-Lineage Lymphomas.

作者信息

Atar Daniel, Mast Anna-Sophia, Scheuermann Sophia, Ruoff Lara, Seitz Christian Martin, Schlegel Patrick

机构信息

Department of Pediatric Hematology and Oncology, University of Tuebingen, 72076 Tuebingen, Germany.

DFG Cluster of Excellence 2180 Image-Guided and Functional Instructed Tumor Therapy (iFIT), University of Tuebingen, 72076 Tuebingen, Germany.

出版信息

Biomedicines. 2022 Sep 28;10(10):2420. doi: 10.3390/biomedicines10102420.

Abstract

CD19CAR T cells facilitate a transformational treatment in various relapsed and refractory aggressive B-lineage cancers. In general, encouraging response rates have been observed in B-lineage-derived non-Hodgkin's lymphomas treated with CD19CAR T cells. The major cause of death in heavily pretreated NHL patients is lymphoma progression and lymphoma recurrence. Inefficient CAR T cell therapy is the result of the limited potency of the CAR T cell product or is due to loss of the targeted antigen. Target antigen loss has been identified as the key factor that can be addressed stringently by dual- or multitargeted CAR T cell approaches. We have developed a versatile adapter CAR T cell technology (AdCAR) that allows multitargeting. Screening of three different B-lineage lymphoma cell lines has revealed distinct immune target profiles. Cancer-specific adapter molecule combinations may be utilized to prevent antigen immune escape. In general, CD19CAR T cells become non-functional in CD19 negative lymphoma subsets; however, AdCAR T cells can be redirected to alternative target antigens beyond CD19, such as CD20, CD22, CD79B, and ROR-1. The capability to flexibly shift CAR specificity by exchanging the adapter molecule's specificity broadens the application and significantly increases the anti-leukemic and anti-lymphoma activity. The clinical evaluation of AdCAR T cells in lymphoma as a new concept of CAR T cell immunotherapy may overcome treatment failure due to antigen immune escape in monotargeted conventional CAR T cell therapies.

摘要

CD19嵌合抗原受体T细胞(CD19CAR T细胞)为多种复发难治性侵袭性B细胞系癌症带来了变革性治疗方法。总体而言,在用CD19CAR T细胞治疗的B细胞系来源的非霍奇金淋巴瘤中观察到了令人鼓舞的缓解率。接受过大量预处理的非霍奇金淋巴瘤(NHL)患者的主要死亡原因是淋巴瘤进展和复发。CAR T细胞治疗效率低下是由于CAR T细胞产品效力有限或靶向抗原丢失所致。靶向抗原丢失已被确定为可通过双靶点或多靶点CAR T细胞方法严格解决的关键因素。我们开发了一种多功能衔接子CAR T细胞技术(AdCAR),可实现多靶点作用。对三种不同的B细胞系淋巴瘤细胞系进行筛选,揭示了不同的免疫靶点特征。可利用癌症特异性衔接子分子组合来防止抗原免疫逃逸。一般来说,CD19CAR T细胞在CD19阴性淋巴瘤亚群中失去功能;然而,AdCAR T细胞可重新靶向CD19以外的其他靶抗原,如CD20、CD22、CD79B和ROR-1。通过交换衔接子分子的特异性来灵活改变CAR特异性的能力拓宽了其应用范围,并显著提高了抗白血病和抗淋巴瘤活性。AdCAR T细胞作为CAR T细胞免疫疗法的新概念在淋巴瘤中的临床评估可能会克服单靶点传统CAR T细胞疗法中因抗原免疫逃逸导致的治疗失败。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5df3/9599140/971e09341f1b/biomedicines-10-02420-g001.jpg

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