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T 细胞衔接器治疗滤泡性淋巴瘤的格局

英文原题:The landscape of T-cell engagers for the treatment of follicular lymphoma.

查看英文原题

The landscape of T-cell engagers for the treatment of follicular lymphoma.

PubMed 2024/10/08(内容时间) Oncoimmunology Q1 · IF 6.2(JCR 2025)

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中文摘要

滤泡性淋巴瘤(FL)是非霍奇金淋巴瘤第二常见的亚型,其生存和进展依赖于与肿瘤微环境中免疫元素的相互作用,包括T滤泡辅助细胞和滤泡树突状细胞。尽管FL对化学免疫治疗初始有反应,但通常被认为不可治愈。改善FL免疫介导控制的策略可显著惠及该人群,尤其是该人群包含许多老年和合并症患者。免疫细胞衔接器,尤其是双特异性抗体(BsAbs),通过桥接肿瘤细胞和效应细胞,从而触发T细胞活化和细胞毒性杀伤,在靶向FL中至关重要。CD3 × CD20 BsAbs在B-NHL患者的临床开发中展现出最大前景,其结构变异影响其靶点亲和力和效力。本综述总结了BsAbs用于复发/难治性FL的当前临床试验,重点介绍了一些药物的获批、其在一线治疗或联合治疗中的作用、其毒性特征,以及与其他免疫细胞疗法相比该治疗方法的未来。

展开英文摘要原文

Follicular lymphoma (FL), the second most common subtype of non-Hodgkin lymphoma, relies on interactions with immune elements in the tumor microenvironment, including T-follicular helper cells and follicular dendritic cells, for its survival and progression. Despite its initial responsiveness to chemoimmunotherapy, FL is generally considered incurable. Strategies to improve immune-mediated control of FL could significantly benefit this population, particularly as it includes many elderly and comorbid patients.

Immune cell engagers, especially bispecific antibodies (BsAbs), are crucial in targeting FL by bridging tumor and effector cells, thereby triggering T-cell activation and cytotoxic killing. CD3 × CD20 BsAbs have shown the most promise in clinical development for B-NHL patients, with structural variations affecting their target affinity and potency.

This review summarizes the current clinical trials of BsAbs for relapsed/refractory FL, highlighting the approval of some agents, their role in first-line treatment or combination therapies, their toxicity profiles, and the future of this therapeutic approach compared to other immune cell therapies.

论文信息

作者
Rivas-Delgado A、Landego I、Falchi L
单位
Department of Medicine, Lymphoma Service, Memorial Sloan Kettering Cancer Center, New York, USA.United States
文献类型
综述 · 美国 NIH 资助研究 · 非美国政府资助研究
期刊
Oncoimmunology2024
原文标识
PubMed 39398477 · DOI 10.1080/2162402X.2024.2412869