纳米体及其衍生物:开创癌症免疫治疗的未来。

IF 8.2 2区 生物学 Q1 CELL BIOLOGY
Haixia Li, Quan Zhou, Nan Cao, Chenghao Hu, Jincheng Wang, Yu He, Shan Jiang, Qi Li, Miao Chen, Li Gong, Ming Luo, Xinzhou Deng, Zhiguo Luo
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引用次数: 0

摘要

癌症免疫疗法是一种增强免疫系统识别和攻击恶性细胞的疗法,它彻底改变了传统的癌症治疗模式。嵌合抗原受体T细胞(CAR-T)疗法和免疫检查点抑制剂(ICIs)等方法已经证明了有希望的治疗效果,导致美国食品和药物管理局(FDA)在过去几十年中批准了许多免疫肿瘤药物。肿瘤免疫制剂在肿瘤免疫治疗中有着广泛的应用,主要是基于传统的全长抗体或其衍生物。然而,它们的大尺寸、不需要的免疫原性、低溶解度、复杂的分子结构和有限的肿瘤穿透性构成了必须解决的重大挑战。纳米体是源自骆驼重链免疫球蛋白可变区域的单域抗体片段,是已知最小的抗原结合片段。除了它们的小尺寸(~ 15 kDa)外,纳米体还具有一系列有利的特性,包括高稳定性,对靶抗原的强特异性和亲和力,低免疫原性和成本效益。然而,它们的血清半衰期短和缺乏Fc介导的功能可能会限制疗效,这可以通过Fc融合、白蛋白结合或多价结构设计来解决。这些特性使纳米体能够支持多功能结构,如双特异性car、分泌纳米体的car、双含ici分子和三特异性免疫细胞结合抗体。近年来,越来越多的基于纳米体的免疫肿瘤药物进入临床前和临床试验阶段,其中一些产品已获得美国FDA和中国国家药品监督管理局批准用于癌症治疗。在这篇综述中,我们探讨了纳米体的独特特性,并全面总结了基于纳米体的免疫肿瘤药物的临床前和临床进展,重点是它们在CAR-T细胞、ICIs和免疫细胞结合抗体中的应用。通过将创新分子工程与转化临床开发相结合的独特能力,纳米体疗法有望彻底改变当前癌症免疫治疗的范式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nanobodies and their derivatives: pioneering the future of cancer immunotherapy.

Cancer immunotherapy, which boosts the immune system to recognize and attack malignant cells, has revolutionized traditional cancer treatment paradigms. Approaches such as chimeric antigen receptor T cell (CAR-T) therapy and immune checkpoint inhibitors (ICIs) have demonstrated promising therapeutic outcomes, leading to the approval of numerous immuno-oncology agents by the US Food and Drug Administration (FDA) over the past few decades. Immuno-oncology agents, mainly based on conventional full-length antibodies or their derivatives, are widely used in cancer immunotherapy. However, their large size, unwanted immunogenicity, poor solubility, complex molecular architectures, and limited tumor penetration pose significant challenges that must be addressed. Nanobodies, which are single-domain antibody fragments originating from the variable regions of camelid heavy-chain immunoglobulins, represent the smallest known antigen-binding fragments. In addition to their small size (~ 15 kDa), nanobodies possess a range of advantageous properties, including high stability, strong specificity and affinity for target antigens, low immunogenicity, and cost-effective production. Nonetheless, their short serum half-life and lack of Fc-mediated functions may limit efficacy, which can be addressed by Fc fusion, albumin binding, or multivalent construct design. These properties enable nanobodies to support multifunctional constructs, such as bispecific CARs, nanobody-secreting CARs, dual ICI-containing molecules, and trispecific immune cell-engaging antibodies. In recent years, a growing number of nanobody-based immuno-oncology agents have progressed into preclinical and clinical trials, with several products approved by the US FDA and China's National Medical Products Administration for cancer therapy. In this review, we explore the unique properties of nanobodies and provide a comprehensive summary of recent preclinical and clinical advancements in nanobody-based immuno-oncology agents, with a focus on their applications in CAR-T cells, ICIs, and immune cell-engaging antibodies. Through their unique capacity to integrate innovative molecular engineering with translational clinical development, nanobody-based therapeutics are poised to revolutionize current paradigms in cancer immunotherapy.

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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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