Promoting macrophage phagocytosis of cancer cells for effective cancer immunotherapy.

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Lei Wang, Ziyi Hu, Wencan Zhang, Zhixin Wang, Ming Cao, Xu Cao
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引用次数: 0

Abstract

Cancer therapy has been revolutionized by immunotherapeutic agents exploiting adaptive antitumor immunity in the past two decades. However, the overall response rate of these immunotherapies is limited, and patients also develop resistance upon treatment, promoting a rapidly growing exploration of anti-tumor innate immunity for effective cancer therapy. Among these, macrophage immunotherapy through harnessing macrophage phagocytosis has been thrust into the spotlight due to its potential for simultaneously inducing cancer cell killing effect and mobilizing adaptive antitumor responses. Here in this review, we summarize the current macrophage immunotherapy such as therapeutic antibodies, phagocytosis checkpoint blockades, and CAR-macrophages with a particular emphasis on the resistant mechanisms limiting their therapeutic effects. Moreover, we further survey the efforts being placed to seek synergistic mechanisms and combination strategies for promoting macrophage phagocytosis which might stand as next-generation cancer immunotherapy.

促进巨噬细胞吞噬癌细胞,实现有效的癌症免疫疗法。
过去二十年来,利用适应性抗肿瘤免疫的免疫治疗药物给癌症治疗带来了革命性的变化。然而,这些免疫疗法的总体反应率有限,患者在接受治疗后还会产生抗药性,这促使人们开始快速探索抗肿瘤先天免疫,以有效治疗癌症。其中,利用巨噬细胞吞噬功能的巨噬细胞免疫疗法因其同时诱导癌细胞杀伤效应和调动适应性抗肿瘤反应的潜力而备受关注。在这篇综述中,我们总结了目前的巨噬细胞免疫疗法,如治疗性抗体、吞噬检查点阻断剂和 CAR-巨噬细胞,并特别强调了限制其治疗效果的抗药性机制。此外,我们还进一步调查了目前为寻求促进巨噬细胞吞噬的协同机制和组合策略所做的努力,这可能会成为下一代癌症免疫疗法。
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
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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