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用于治疗 B 系淋巴瘤的衔接器 CAR-T 细胞疗法

英文原题:Adapter CAR T Cell Therapy for the Treatment of B-Lineage Lymphomas.

查看英文原题

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

PubMed 2022/09/28(内容时间) Biomedicines Q2 · IF 4.5(JCR 2025)

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中文摘要

CD19CAR-T 细胞促进了多种复发/难治性侵袭性B系癌症的变革性治疗。总体而言,在采用CD19CAR-T 细胞治疗的B系来源非霍奇金淋巴瘤中,已观察到令人鼓舞的缓解率。在重度预处理的NHL患者中,主要死亡原因是淋巴瘤进展和淋巴瘤复发。CAR-T 细胞治疗效率低下是CAR-T 细胞产品效力有限的结果,或是由于靶抗原丢失所致。靶抗原丢失已被确定为关键因素,可通过双靶点或多靶点CAR-T 细胞方法严格解决。

我们开发了一种多功能的适配器CAR-T 细胞技术(AdCAR),可实现多靶点靶向。对三种不同B系淋巴瘤细胞系的筛选揭示了不同的免疫靶点谱。癌症特异性适配器分子组合可用于防止抗原免疫逃逸。

总体而言,CD19CAR-T 细胞在CD19阴性淋巴瘤亚群中变得无功能;然而,AdCAR T细胞可以重新定向至CD19以外的替代靶抗原,如CD20、CD22、CD79B和ROR-1。通过交换适配器分子的特异性来灵活转换CAR特异性的能力拓宽了应用范围,并显著提高了抗白血病和抗淋巴瘤活性。AdCAR T细胞在淋巴瘤中的临床评估作为CAR-T 细胞免疫治疗的新概念,可能克服单靶点常规CAR-T 细胞治疗中因抗原免疫逃逸导致的治疗失败。

展开英文摘要原文

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.

论文信息

作者
Atar D、Mast AS、Scheuermann S、Ruoff L、Seitz CM、Schlegel P
单位
Department of Pediatric Hematology and Oncology, University of Tuebingen, 72076 Tuebingen, Germany.Germany
期刊
Biomedicines2022 Sep 28
原文标识
PubMed 36289682 · DOI 10.3390/biomedicines10102420