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An immunostimulatory dual-functional nanocarrier that improves cancer immunochemotherapy

Immunochemotherapy combines a chemotherapeutic agent with an immune-modulating agent and represents an attractive approach to improve cancer therapy. However, the success of immunochemotherapy is hampered by the lack of a strategy to effectively co-deliver the two therapeutics to the tumours. Here w...

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Detalles Bibliográficos
Autores principales: Chen, Yichao, Xia, Rui, Huang, Yixian, Zhao, Wenchen, Li, Jiang, Zhang, Xiaolan, Wang, Pengcheng, Venkataramanan, Raman, Fan, Jie, Xie, Wen, Ma, Xiaochao, Lu, Binfeng, Li, Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103075/
https://www.ncbi.nlm.nih.gov/pubmed/27819653
http://dx.doi.org/10.1038/ncomms13443
Descripción
Sumario:Immunochemotherapy combines a chemotherapeutic agent with an immune-modulating agent and represents an attractive approach to improve cancer therapy. However, the success of immunochemotherapy is hampered by the lack of a strategy to effectively co-deliver the two therapeutics to the tumours. Here we report the development of a dual-functional, immunostimulatory nanomicellar carrier that is based on a prodrug conjugate of PEG with NLG919, an indoleamine 2,3-dioxygenase (IDO) inhibitor currently used for reversing tumour immune suppression. An Fmoc group, an effective drug-interactive motif, is also introduced into the carrier to improve the drug loading capacity and formulation stability. We show that PEG(2k)-Fmoc-NLG alone is effective in enhancing T-cell immune responses and exhibits significant antitumour activity in vivo. More importantly, systemic delivery of paclitaxel (PTX) using the PEG(2k)-Fmoc-NLG nanocarrier leads to a significantly improved antitumour response in both breast cancer and melanoma mouse models.