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纳米抗体及其衍生物:开创肿瘤免疫治疗的未来

英文原题:Nanobodies and their derivatives: pioneering the future of cancer immunotherapy.

PubMed 2025/06/05(内容时间) Cell Commun Signal Q1 · IF 11.6(JCR 2025)

研究概要

癌症免疫治疗通过增强免疫系统识别和攻击恶性细胞的能力,彻底改变了传统的癌症治疗范式。

中文摘要

通过增强免疫系统识别并攻击恶性细胞,癌症免疫治疗彻底改变了传统癌症治疗模式。CAR-T 细胞治疗和免疫检查点抑制剂(ICI)等方法取得有前景的治疗结局,促使美国食品药品监督管理局(FDA)在过去数十年批准了多种免疫肿瘤学药物。免疫肿瘤学药物主要基于传统全长抗体或其衍生物,已广泛用于癌症免疫治疗。然而,这些药物体积较大、可能产生不必要的免疫原性、溶解性差、分子结构复杂且肿瘤穿透能力有限,因而存在亟需解决的重要挑战。纳米抗体是源自骆驼科重链免疫球蛋白可变区的单域抗体片段,是已知最小的抗原结合片段。除体积小(约15 kDa)外,纳米抗体还具有多种优势,包括稳定性高、对靶抗原特异性和亲和力强、免疫原性低且生产成本较低。不过,其血清半衰期短且缺少Fc介导功能,可能限制疗效;可通过Fc融合、白蛋白结合或设计多价结构来改善。上述特性使纳米抗体可支持多功能构建体,如双特异性CAR、分泌纳米抗体的CAR、含双重ICI的分子及三特异性免疫细胞衔接抗体。近年来,越来越多基于纳米抗体的免疫肿瘤学药物进入临床前和临床试验,其中多种产品已获美国FDA和中国国家药品监督管理局批准用于癌症治疗。本综述探讨纳米抗体的独特性质,并全面总结基于纳米抗体的免疫肿瘤学药物近期临床前及临床进展,重点讨论其在CAR-T细胞、ICI和免疫细胞衔接抗体中的应用。凭借整合创新分子工程与临床转化开发的独特能力,纳米抗体疗法有望改变当前癌症免疫治疗模式。

展开英文摘要原文

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.

论文信息

作者
Li H、Zhou Q、Cao N、Hu C、Wang J、He Y、Jiang S、Li Q
第一作者单位
Department of Clinical Oncology, Hubei Provincial Clinical Research Center for precision Diagnosis and Treatment of liver cancer, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, 442000, P.R. China. lihaixia@hbmu.edu.cn.China
通讯作者单位
Department of Clinical Oncology, Hubei Provincial Clinical Research Center for precision Diagnosis and Treatment of liver cancer, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, 442000, P.R. China. zhiguo_luo@126.com.China
文献类型
综述
期刊
Cell communication and signaling : CCS2025 Jun 5
原文标识
PubMed 40474230 · DOI 10.1186/s12964-025-02270-4