2皮の现菌による新たながん治療ぞのアプロヌチ「AUN(阿吜)」を開発免疫䞍党状態でも機胜が期埅されるがん治療に向けお

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2025-08-06 北陞先端科孊技術倧孊院倧孊,筑波倧孊,科孊技術振興機構

北陞先端科孊技術倧孊院倧孊ず筑波倧孊、第䞀䞉共による共同研究で、免疫现胞に䟝存しない新たながん治療アプロヌチ「AUN(阿吜)」が開発された。これは、がん内に存圚する现菌Proteus mirabilis(阿圢)ず光合成现菌Rhodopseudomonas palustris(吜圢)が連携し、腫瘍血管やがん现胞を遞択的に砎壊する技術。免疫䞍党状態の患者でも効果が期埅され、副䜜甚も抑制可胜。成果はNature Biomedical Engineering誌に掲茉された。

2皮の现菌による新たながん治療ぞのアプロヌチ「AUN(阿吜)」を開発免疫䞍党状態でも機胜が期埅されるがん治療に向けお

<関連情報>

腫瘍内に存圚する腫瘍溶解性现菌は、遞択的な腫瘍内血栓圢成ず壊死を通じお匷力な抗がん効果を匕き起こす Tumour-resident oncolytic bacteria trigger potent anticancer effects through selective intratumoural thrombosis and necrosis

Seigo Iwata,Taisei Nishiyama,Matomo Sakari,Yuki Doi,Naoki Takaya,Yusuke Ogitani,Hiroshi Nagano,Keisuke Fukuchi & Eijiro Miyako
Nature Biomedical Engineering  Published:05 August 2025
DOI:https://doi.org/10.1038/s41551-025-01459-9

Abstract

Intratumoural bacteria represent a promising drug-free strategy in cancer therapy. Here we demonstrate that a tumour-resident bacterial consortium—Proteus mirabilis (A-gyo) and Rhodopseudomonas palustris (UN-gyo)—in a precise 3:97 ratio (A-gyo:UN-gyo), exhibits potent antitumour efficacy independent of immune cell infiltration. In both immunocompetent and immunocompromised mouse models, including human tumour xenografts, intravenous administration of the bacterial consortium led to complete tumour remission, prolonged survival, and no observable systemic toxicity or cytokine release syndrome. Genomic and phenotypic analyses revealed A-gyo’s unique non-pathogenic profile and impaired motility, while UN-gyo modulated A-gyo’s biogenic activity, enhanced safety and promoted cancer-specific transformation. Mechanistically, the bacterial consortium triggered selective intratumoural thrombosis and vascular collapse—supported by cytokine induction, fibrin deposition and platelet aggregation—culminating in widespread tumour necrosis. The consortium also proliferated within tumours, formed biofilms and exerted direct oncolytic effects. This natural bacterial synergy—achieved without genetic engineering—offers a self-regulating and controllable strategy for safe, tumour-targeted therapy.

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