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从筛选到应用:适配体作为血液学中的靶向试剂

英文原题:From Selection to Use: Aptamers as Targeting Reagents in Hematology.

查看英文原题

From Selection to Use: Aptamers as Targeting Reagents in Hematology.

PubMed 2026/02/27(内容时间) Biomedicines Q2 · IF 4.5(JCR 2025)

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中文摘要

适配体是合成核酸配体,已被提出作为靶向分子和细胞的抗体替代品。在血液学中,大多数综述围绕疾病或技术平台来组织适配体文献。这种框架掩盖了不同血细胞类型被覆盖的不均衡程度。在本综述中,我们按血细胞谱系展示已开发的适配体。具体而言,我们考察了针对B细胞、T细胞、NK 细胞和红细胞的适配体。这种组织方式揭示出研究强烈集中于一小部分经典表面标志物以及恶性细胞模型。与此同时,在区分分化阶段或功能细胞状态的适配体方面也出现了空白。在这一框架内,我们评估了已报道的应用、设计策略和实验用例,以及靶点选择和生物学分辨率方面持续存在的局限。我们的分析凸显了当前血液细胞靶向适配体研究中的实际约束和概念盲点。总体而言,这些观察界定了一组明确的机会,可将适配体开发拓展至更具状态分辨率、更具生物学信息价值且更具临床相关性的靶向策略。

展开英文摘要原文

Aptamers are synthetic nucleic acid ligands that have been proposed as alternatives to antibodies for targeting molecules and cells. In hematology, most reviews have organized aptamer literature around diseases or technological platforms. This framing has obscured how unevenly different blood cell types have been covered. In this review, we present developed aptamers organized by blood cell lineages. Specifically, we examine aptamers for B cells, T cells, natural killer cells, and red blood cells.

This organization revealed a strong concentration on a small set of canonical surface markers and on malignant cell models. A parallel gap appeared in aptamers that distinguish differentiation stages or functional cell states. Within this framework, we evaluated reported applications, design strategies, and experimental use cases alongside persistent limitations in target selection and biological resolution.

Our analysis highlighted both practical constraints and conceptual blind spots in current blood-cell-targeting aptamer research.

Together, these observations defined a set of clear opportunities for expanding aptamer development toward more state-resolved, biologically informative, and clinically relevant targeting strategies.

论文信息

作者
Albert B、Ebanks F、Gharagozloo K、Hai X、Ngu R、Munting S、McKeague M
单位
Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montréal, QC H3A 0B8, Canada.Canada
文献类型
综述
期刊
Biomedicines2026 Feb 27
原文标识
PubMed 41898181 · DOI 10.3390/biomedicines14030534