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儿童急性淋巴细胞白血病的抗体和细胞疗法:机制与前景

英文原题:Antibody and Cellular-Based Therapies for Pediatric Acute Lymphoblastic Leukemia: Mechanisms and Prospects.

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Antibody and Cellular-Based Therapies for Pediatric Acute Lymphoblastic Leukemia: Mechanisms and Prospects.

PubMed 2022/04/07(内容时间) Pharmacology Q3 · IF 2.8(JCR 2025)

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研究概要

讨论了显著的前景和挑战,重点介绍了应对 ALL 的创新免疫疗法。总之,本综述将总结儿童 ALL 抗体和细胞疗法的进展,这可能促进基于抗体的生物制药的进一步研究。

研究思路结论见上方概要

急性淋巴细胞白血病(ALL)是儿童中最常被诊断的癌症之一。尽管过去十年在治疗 ALL 方面付出了巨大努力,但传统化疗策略的强度已达到耐受极限。在近期开发的多种治疗方法中,抗体和细胞基础疗法显示出较低的毒性和较好的疗效。总结:由于先进的机制作用,这些创新疗法在根除儿童 ALL,尤其是难治/复发性 ALL 患者方面,提供了持久缓解和长期生存。鉴于这些方面,本文重点阐述靶向肿瘤抗原的抗体、抗体药物偶联物、双特异性抗体和CAR-T 细胞的作用机制和应用现状。

展开英文摘要原文

BACKGROUND: Acute lymphoblastic leukemia (ALL) is one of the most commonly diagnosed cancers in children. Despite enormous efforts to treat ALL over the past decade, the intensity of conventional chemotherapeutic strategies has reached the tolerance limit. Among various recently developed therapeutic approaches, antibody and cellular-based therapies showed less toxicity and better curative effect. SUMMARY: Due to advanced mechanistic actions, these innovative therapies have provided durable responses and long-term survival in eradicating pediatric ALL, especially patients with refractory/relapsed ALL. Owing to these aspects, herein, we emphasize the mechanisms of action and application status of antibodies targeting tumor antigens, antibody-drug conjugates, bispecific antibodies, and chimeric antigen receptor T cells. KEY MESSAGES: The significant prospects and challenges are discussed, highlighting the innovative immunotherapies to deal with ALL. Together, this review will summarize the progress of antibody and cellular-based therapies for pediatric ALL, which may promote further research on antibody-based biopharmaceutics.

论文信息

作者
Li W、Zhang Y、Kankala RK、Zou L、Chen Z
第一作者单位
School of Basic Medical Sciences, Chengdu University, Chengdu, China.China
通讯作者单位
School of Food and Bioengineering, Institute for Advanced Study, Chengdu University, Chengdu, China.China
文献类型
综述
期刊
Pharmacology2022
原文标识
PubMed 35390793 · DOI 10.1159/000524040