再発腫瘍を抑制する個別化がんワクチンを開発(UW researchers develop personalized cancer vaccines that slow tumor recurrence in mice)

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2025-06-19 ウィスコンシン大学マディソン校(UW-Madison)

再発腫瘍を抑制する個別化がんワクチンを開発(UW researchers develop personalized cancer vaccines that slow tumor recurrence in mice)
This image shows the formation of pyroptotic vesicles, which look like small bubbles, in cancer cells as they undergo programmed cell death. A team of researchers led by UW–Madison pharmacy professor Quanyin Hu have developed a method for harnessing these vesicles to deliver vaccines against tumors with a high rate of recurrence. Image courtesy of Quanyin Hu

ウィスコンシン大学の研究チームは、がん細胞死で生じる「ピロプトーシス小胞」を活用し、個別化がんワクチンを開発。小胞内の腫瘍抗原と免疫刺激薬をハイドロゲルに封入し、腫瘍切除後の部位に移植することで、強力な免疫応答を誘導し再発を抑制。三重陰性乳がんやメラノーマのマウス実験で有効性が確認され、生存期間も延長。他のワクチンより高い効果が見られ、再発傾向のある多様ながんに応用可能な新たな免疫療法として期待されている。

<関連情報>

個別化がんワクチンとしてのパイロプトーシス小胞の工学的研究 Engineering pyroptotic vesicles as personalized cancer vaccines

Zhaoting Li,Yixin Wang,Fanyi Mo,Tyler Wolter,Rachel Hong,Allie Barrett,Nathaniel Richmond,Fengyuan Liu,Yu Chen,Xicheng Yang,Lauren Dempsey & Quanyin Hu
Nature Nanotechnology  Published:16 May 2025
DOI:https://doi.org/10.1038/s41565-025-01931-2

Abstract

Tumour vaccines are designed to stimulate the host’s immune system against existing tumours or tumour recurrence. However, individual differences, tumour heterogeneity and side effects hinder the applications of current tumour vaccines and require the development of personalized cancer vaccines. To overcome these challenges, we engineered pyroptotic vesicles—extracellular vesicles formed during tumour cell pyroptosis—as a tumour vaccine platform. The extracted pyroptotic vesicles possess abundant tumour antigens and potent immune-stimulating ability and, loaded into a biocompatible hydrogel, they can be implanted into post-surgical tumour cavities to prevent tumour recurrence. The pyroptotic-vesicle-based vaccine outperforms both exosome- and apoptotic-body-based vaccines in inhibiting tumour recurrence and metastasis in different post-surgical mouse models. Mechanistic studies reveal that the pyroptotic-vesicle-based vaccine could stimulate robust antigen-specific dendritic cell and T cell immune responses against both artificial OVA antigens and cancer neoantigens. In sum, our vaccine platform can be tailored to stimulate robust antitumour immune responses for treating individual cancer patients.

医療・健康
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