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Xuefei Zhou

Researcher at University of North Carolina at Chapel Hill

Publications -  16
Citations -  650

Xuefei Zhou is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Gene delivery & Transfection. The author has an hindex of 8, co-authored 16 publications receiving 357 citations. Previous affiliations of Xuefei Zhou include Zhejiang University.

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Nonviral cancer gene therapy: Delivery cascade and vector nanoproperty integration.

TL;DR: This review analyzes the cancer gene‐delivery cascade and the barriers, the needed nanopro properties and the current strategies for overcoming these barriers, and outlines PEGylation, surface‐charge, size, and stability dilemmas in vector nanoproperties to efficiently accomplish the cancer genes delivery cascade.
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Relaxin gene delivery mitigates liver metastasis and synergizes with check point therapy

TL;DR: In colorectal, pancreatic, and breast cancer liver metastasis models, the RLN gene therapy results in significant inhibition of metastatic progression and prolongs survival and the combination of the RLNs gene therapy with PD-L1 blockade immunotherapy produces a synergistic anti-metastatic efficacy.
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Nanoparticle-enhanced chemo-immunotherapy to trigger robust antitumor immunity.

TL;DR: A novel strategy combining chemotherapy and immunotherapy to modulate the TME by systemically and concurrently delivering the chemotherapeutic agent SN38 and the STING agonist DMXAA into tumors shows potent therapeutic efficacy in three mice tumor models and elicits remarkable therapeutic benefit when combined with anti–PD-1 therapy.
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Macrophage-Mediated Tumor Cell Phagocytosis: Opportunity for Nanomedicine Intervention.

TL;DR: Intervention of macrophage phagocytosis by blocking anti‐phagocytic signals on live tumor cells or inhibiting tumor efferocyTosis presents a promising strategy for the development of cancer immunotherapies.
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Celastrol nanoemulsion induces immunogenicity and downregulates PD-L1 to boost abscopal effect in melanoma therapy.

TL;DR: It is shown that celastrol (CEL) induced not only strong ICD but also downregulation of PD-L1 expression of tumor cells, demonstrating a new and much cost-effective immunotherapy strategy - chemotherapy-induced immunotherapy against melanoma without the need for expensive immune-checkpoint inhibitors.