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体积更小、效力更强——靶向肿瘤相关糖类抗原的小抗体片段最新进展

英文原题:Smaller size packs a stronger punch - Recent advances in small antibody fragments targeting tumour-associated carbohydrate antigens.

查看英文原题

Smaller size packs a stronger punch - Recent advances in small antibody fragments targeting tumour-associated carbohydrate antigens.

PubMed 2023/05/15(内容时间) Theranostics Q1 · IF 14.9(JCR 2025)

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中文摘要

附着于蛋白质、脂质或形成长而复杂的链,聚糖代表了自然界中最通用的翻译后修饰,并包围着所有人类细胞。独特的聚糖结构被免疫系统监测,并区分自我与非自我以及健康细胞与恶性细胞。异常的糖基化,称为肿瘤相关碳水化合物抗原(TACAs),是癌症的标志,并与癌症生物学的各个方面相关。因此,TACAs代表了用于癌症诊断和治疗的 monoclonal antibodies 的有吸引力的靶点。然而,由于厚而密集的糖萼以及肿瘤微环境,常规抗体在体内往往受到访问受限和有效性有限的困扰。为了克服这个问题,许多小型抗体片段应运而生,显示出与全长对应物相似的亲和力但更好的效率。在这里,我们综述了针对肿瘤细胞上特定聚糖的小型抗体片段,并强调了它们相对于常规抗体的优势。

展开英文摘要原文

Attached to proteins, lipids, or forming long, complex chains, glycans represent the most versatile post-translational modification in nature and surround all human cells. Unique glycan structures are monitored by the immune system and differentiate self from non-self and healthy from malignant cells. Aberrant glycosylations, termed tumour-associated carbohydrate antigens (TACAs), are a hallmark of cancer and are correlated with all aspects of cancer biology.

Therefore, TACAs represent attractive targets for monoclonal antibodies for cancer diagnosis and therapy.

However, due to the thick and dense glycocalyx as well as the tumour micro-environment, conventional antibodies often suffer from restricted access and limited effectiveness in vivo . To overcome this issue, many small antibody fragments have come forth, showing similar affinity with better efficiency than their full-length counterparts.

Here we review small antibody fragments against specific glycans on tumour cells and highlight their advantages over conventional antibodies.

论文信息

作者
Khilji SK、Op 't Hoog C、Warschkau D、Lühle J、Goerdeler F、Freitag A、Seeberger PH、Moscovitz O
单位
Department of Biomolecular Systems, Max Planck Institute of Colloids and Interfaces, 14476 Potsdam, Germany.Germany
文献类型
综述 · 非美国政府资助研究
期刊
Theranostics2023
原文标识
PubMed 37284439 · DOI 10.7150/thno.80901