| Literature DB >> 30014609 |
Yannan Yang1, Jie Tang1, Prasanna Lakshmi Abbaraju1, Manasi Jambhrunkar1, Hao Song1, Min Zhang1, Chang Lei1, Jianye Fu1, Zhengying Gu1, Yang Liu1, Chengzhong Yu1.
Abstract
Immunosuppressive tumors generally exhibit poor response to immune checkpoint blockade based cancer immunotherapy. Rationally designed hybrid nanoreactors are now presented that have integrated functions as Fenton catalysts and glutathione depletion agents for amplifying the immunogenic cell death and activating immune cells. A simple physical mixture of nanoreactors and chemodrugs in combination with immune checkpoint blockades show synergistically and concurrently enhanced chemo-immunotherapy efficacy, inhibiting the growth of both treated primary immunosuppressive tumors and untreated distant tumors. The off-the-shelf strategy uses tumor antigens generated in situ and avoids cargo loading, and is thus a substantial advance in personalized nanomedicine for clinical translation.Entities:
Keywords: chemoimmunotherapy; immune checkpoint blockades; immunogenic cell death; immunosuppressive tumors; nanoreactors
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Year: 2018 PMID: 30014609 DOI: 10.1002/anie.201807595
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336