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基于CCR4的皮肤T细胞淋巴瘤治疗现状的叙述性综述:聚焦于莫加莫单抗及未来治疗

A Narrative Review of the State of the Art of CCR4-Based Therapies in Cutaneous T-Cell Lymphomas: Focus on Mogamulizumab and Future Treatments.

作者信息

Zengarini Corrado, Guglielmo Alba, Mussi Martina, Motta Giovanna, Agostinelli Claudio, Sabattini Elena, Piraccini Bianca Maria, Pileri Alessandro

机构信息

Department of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138 Bologna, Italy.

Dermatology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.

出版信息

Antibodies (Basel). 2024 Apr 22;13(2):32. doi: 10.3390/antib13020032.

DOI:10.3390/antib13020032
PMID:38804300
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11130839/
Abstract

The CCR4 receptor is a pivotal target in cutaneous T-cell lymphoma (CTCL) therapy due to its role in impairing immune responses against malignant T-cells and expression profiles. Monoclonal antibodies like mogamulizumab effectively bind to CCR4, reducing tumour burden and enhancing patient outcomes by inhibiting the receptor's interaction with ligands, thereby hindering malignant T-cell migration and survival. Combining CCR4 antibodies with chemotherapy, radiation, and other drugs is being explored for synergistic effects. Additionally, small-molecular inhibitors, old pharmacological agents interacting with CCR4, and CAR-T therapies are under investigation. Challenges include drug resistance, off-target effects, and patient selection, addressed through ongoing trials refining protocols and identifying biomarkers. Despite advancements, real-life data for most of the emerging treatments are needed to temper expectations. In conclusion, CCR4-targeted therapies show promise for CTCL management, but challenges persist. Continued research aims to optimise treatments, enhance outcomes, and transform CTCL management. This review aims to elucidate the biological rationale and the several agents under various stages of development and clinical evaluation with the actual known data.

摘要

CCR4受体是皮肤T细胞淋巴瘤(CTCL)治疗中的一个关键靶点,因为它在损害针对恶性T细胞的免疫反应及表达谱方面发挥作用。像莫加莫单抗这样的单克隆抗体可有效结合CCR4,通过抑制该受体与配体的相互作用来减轻肿瘤负担并改善患者预后,从而阻碍恶性T细胞的迁移和存活。目前正在探索将CCR4抗体与化疗、放疗及其他药物联合使用以产生协同效应。此外,小分子抑制剂、与CCR4相互作用的传统药物以及嵌合抗原受体T细胞(CAR-T)疗法也在研究中。挑战包括耐药性、脱靶效应和患者选择,目前正在通过不断完善方案和识别生物标志物的临床试验来解决这些问题。尽管取得了进展,但仍需要大多数新兴治疗方法的真实数据来调整预期。总之,针对CCR4的疗法对CTCL的治疗显示出前景,但挑战依然存在。持续的研究旨在优化治疗方法、改善治疗效果并变革CTCL的管理。本综述旨在阐明生物学原理以及处于不同开发和临床评估阶段的几种药物及其实际已知数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a833/11130839/b9a0a2563638/antibodies-13-00032-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a833/11130839/b9a0a2563638/antibodies-13-00032-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a833/11130839/b9a0a2563638/antibodies-13-00032-g001.jpg

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