抗原増幅技術として近接標識法を開発(Researchers Develop Proximity Labeling Based Antigen Amplification Technology)

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2025-09-12 中国科学院 (CAS)

中国科学院上海生化細胞所・韓碩教授らの研究チームは、腫瘍免疫療法の課題である「腫瘍抗原の密度不足」に対処する新技術 PATCH(Proximity Amplification and Tagging of Cytotoxic Haptens) を開発し、Nature誌に発表した。PATCHは近接標識技術を免疫調節に初めて応用したもので、腫瘍細胞表面に人工抗原を高密度に「植え付け」ることでT細胞の活性化を劇的に促進する。具体的には、赤色光や超音波で活性化される設計ナノ酵素(PCN)が腫瘍細胞表面で多数のFITC分子を共有結合させ、人工抗原クラスターを形成。これがBiTE(二重特異性T細胞エンゲージャー)と結合し、TCRを効率的に集積してT細胞の腫瘍殺傷能を増強する。動物モデルと患者由来腫瘍サンプルで治療効果が実証され、局所腫瘍の完全消失に加え、未処理腫瘍への遠隔効果(abscopal effect)や長期免疫記憶による再発防止も確認された。本研究は近接標識を検出技術から機能的改変ツールへ拡張し、低毒性かつ高特異性の新世代免疫療法開発に道を拓く。

<関連情報>

近接標識法による抗原誘導性細胞応答の増幅 Amplifying antigen-induced cellular responses with proximity labelling

Shuojun Li,Yinghui Men,Zihan Wang,Yingcheng Wu,Hao Sun,Mingyang Yin,Xinrui Fan,Guiyun Deng,Zhicheng Yang,Tiange Yang,Yudian Xiao,Hu Zhou,Guangchuan Wang,Jia Fan,Chenqi Xu,Qiang Gao & Shuo Han
Nature  Published:10 September 2025
DOI:https://doi.org/10.1038/s41586-025-09518-6

抗原増幅技術として近接標識法を開発(Researchers Develop Proximity Labeling Based Antigen Amplification Technology)

Abstract

Antigen-induced clustering of cell surface receptors, including T cell receptors and Fc receptors, represents a widespread mechanism in cell signalling activation1,2. However, most naturally occurring antigens, such as tumour-associated antigens, stimulate limited receptor clustering and on-target responses owing to insufficient density3,4,5. Here we repurpose proximity labelling6, a method used to biotinylate and identify spatially proximal proteins, to amplify designed probes as synthetic antigen clusters on the cell surface. We develop an in vivo proximity-labelling technology controlled by either red light or ultrasound to covalently tag fluorescein probes at high density near a target antigen. Using T cell receptors as an example, we demonstrate that the amplified fluorescein effectively clusters and directs a fluorescein-binding bispecific T cell engager to induce enhanced T cell activation and cytotoxicity. Noninvasive, tissue-selective labelling in multiple syngeneic mouse tumour models produces potent immune responses that rapidly eradicate treated tumours. Efficient cell lysis further promotes epitope spreading to induce systemic immunity against untreated distal lesions and immune memory against rechallenge. Thus, proximity-labelling chemistry holds promise as a generalized strategy to manipulate antigen-dependent receptor function and cell states.

細胞遺伝子工学
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