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嵌合抗原受体 T 细胞治疗皮肤 T 细胞淋巴瘤:当前的局限性和潜在的治疗策略。

CAR-T cell development for Cutaneous T cell Lymphoma: current limitations and potential treatment strategies.

机构信息

Cartherics Pty Ltd, Notting Hill, VIC, Australia.

Department of Obstetrics and Gynaecology,  Monash University, Clayton, VIC, Australia.

出版信息

Front Immunol. 2022 Aug 18;13:968395. doi: 10.3389/fimmu.2022.968395. eCollection 2022.

Abstract

Chimeric antigen receptor (CAR)-T therapy has demonstrated remarkable outcomes for B cell malignancies, however, its application for T cell lymphoma, particularly cutaneous T cell lymphoma (CTCL), has been limited. Barriers to effective CAR-T cell therapy in treating CTCL include T cell aplasia in autologous transplants, CAR-T product contamination with leukemic T cells, CAR-T fratricide (when the target antigen is present on normal T cells), and tumor heterogeneity. To address these critical challenges, innovative CAR engineering by targeting multiple antigens to strike a balance between efficacy and safety of the therapy is necessary. In this review, we discuss the current obstacles to CAR-T cell therapy and highlight potential targets in treating CTCL. Looking forward, we propose strategies to develop more powerful dual CARs that are advancing towards the clinic in CTCL therapy.

摘要

嵌合抗原受体 (CAR)-T 疗法在治疗 B 细胞恶性肿瘤方面取得了显著的效果,然而,其在 T 细胞淋巴瘤,特别是皮肤 T 细胞淋巴瘤 (CTCL)中的应用受到限制。CAR-T 细胞疗法在治疗 CTCL 中面临的障碍包括自体移植中 T 细胞发育不良、CAR-T 产品被白血病 T 细胞污染、CAR-T 自相残杀(当靶抗原存在于正常 T 细胞上时)和肿瘤异质性。为了解决这些关键挑战,有必要通过靶向多种抗原进行创新的 CAR 工程,以在治疗的疗效和安全性之间取得平衡。在这篇综述中,我们讨论了 CAR-T 细胞治疗目前面临的障碍,并强调了治疗 CTCL 的潜在靶点。展望未来,我们提出了开发更强大的双 CAR 的策略,这些策略正在 CTCL 治疗中推向临床。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e916/9433932/6221c24581b9/fimmu-13-968395-g001.jpg

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