Strategies to enhance anti-leukaemia immunotherapy

IF 4.2 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Memnon Lysandrou, Robert Zeiser
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引用次数: 0

Abstract

Acute myeloid leukaemia (AML) was an incurable disease prior to allogeneic haematopoietic cell transplantation (allo-HCT), which was proven to be a potent cellular immunotherapy-approach. However, allo-HCT has major side effects, with disease relapse presenting as a frequent complication. Novel immunotherapies aim to reduce toxicity and increase the anti-leukaemia activity of allo-HCT. Technological advancements in genetic engineering approaches enable potent immunotherapeutic activity while limiting toxicities. A biology-driven application of small molecules that target AML vulnerabilities holds promise to enhance anti-leukaemia immunotherapy. Extensive preclinical testing of these approaches is essential to reduce toxicity and to find the ideal combination partners for future clinical testing.
加强抗白血病免疫治疗的策略
在同种异体造血细胞移植(allogeneic hematopoietic cell transplantation, alloo - hct)之前,急性髓性白血病(AML)是一种无法治愈的疾病,而同种异体造血细胞移植已被证明是一种有效的细胞免疫治疗方法。然而,同种异体hct有主要的副作用,疾病复发是常见的并发症。新的免疫疗法旨在降低毒性和增加抗白血病活性的同种异体hct。基因工程方法的技术进步使有效的免疫治疗活性,同时限制毒性。靶向AML脆弱性的小分子生物驱动应用有望增强抗白血病免疫治疗。对这些方法进行广泛的临床前试验对于降低毒性和为未来的临床试验找到理想的组合伙伴至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.80
自引率
2.50%
发文量
131
审稿时长
4-8 weeks
期刊介绍: Current Opinion in Pharmacology (COPHAR) publishes authoritative, comprehensive, and systematic reviews. COPHAR helps specialists keep up to date with a clear and readable synthesis on current advances in pharmacology and drug discovery. Expert authors annotate the most interesting papers from the expanding volume of information published today, saving valuable time and giving the reader insight on areas of importance.
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