Unleashing a Dual‐Warhead Nanomedicine to Precisely Sensitize Immunotherapy for Pancreatic Ductal Adenocarcinoma

Despite remarkable achievements in cancer immunotherapy, significant challenges persist in pancreatic ductal adenocarcinoma (PDAC) treatment. Particularly, there is a critical issue of inadequate intratumoral infiltration of effector T cells, primarily attributed to the physical “hard” barrier cause...

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Veröffentlicht in:Advanced functional materials 2024-07, Vol.34 (30), p.n/a
Hauptverfasser: Zhang, Di, Song, Qingxu, Wang, Wenjuan, Li, Qian, Zhao, Zhipeng, Jiang, Yue, Luan, Yuxia
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Sprache:eng
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Zusammenfassung:Despite remarkable achievements in cancer immunotherapy, significant challenges persist in pancreatic ductal adenocarcinoma (PDAC) treatment. Particularly, there is a critical issue of inadequate intratumoral infiltration of effector T cells, primarily attributed to the physical “hard” barrier caused by extracellular matrix (ECM) and the “soft” barrier imposed by immune suppression. Here, a dual‐warhead nanomedicine is reported that effectively targets and attacks the barriers to precisely sensitize PDAC immunotherapy. The nanomedicine is achieved by designing tumor cell membrane vesicle (TMV)‐coated polyamidoamine dendrimer‐condensed siRNA complexes, with hedgehog inhibitor encapsulated in TMV bilayers. With the precision‐guided stealth feature of TMV coating, the nanomedicine achieved powerful tumor‐targeting co‐delivery of hedgehog inhibitor and siRNA, resulting in a significant decrease in collagen I secretion and efficient silencing of the target gene to disrupt the ECM and immune suppression barriers. This nanomedicine enables robust immunity against PDAC progression and metastasis, offering a potent approach to PDAC therapy. A precision‐guided stealth nanomedicine with dual warheads is designed to address the challenges in pancreatic ductal adenocarcinoma (PDAC) treatment, demonstrating potent capability in combating PDAC progression and metastasis. This approach holds great potential for enhancing T cell‐based immunotherapy and improving outcomes in PDAC treatment.
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.202315447