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Journal ArticleDOI

Recent Advances in Cell Membrane-Derived Biomimetic Nanotechnology for Cancer Immunotherapy.

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TLDR
In this article, the use of biomimetic nanotechnology for developing effective cancer immunotherapeutics that demonstrate increased specificity and potency has been discussed, and the recent works and state-of-the-art strategies for anti-tumor immunotherapy are highlighted.
Abstract
Immunotherapy will significantly impact the standard of care in cancer treatment. Recent advances in nanotechnology can improve the efficacy of cancer immunotherapy. However, concerns regarding efficiency of cancer nanomedicine, complex tumor microenvironment, patient heterogeneity, and systemic immunotoxicity drive interest in more novel approaches to be developed. For this purpose, biomimetic nanoparticles are developed to make innovative changes in the delivery and biodistribution of immunotherapeutics. Biomimetic nanoparticles have several advantages that can advance the clinical efficacy of cancer immunotherapy. Thus there is a greater push toward the utilization of biomimetic nanotechnology for developing effective cancer immunotherapeutics that demonstrate increased specificity and potency. The recent works and state-of-the-art strategies for anti-tumor immunotherapeutics are highlighted here, and particular emphasis has been given to the applications of cell-derived biomimetic nanotechnology for cancer immunotherapy.

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Nanocatalyst-Mediated Chemodynamic Tumor Therapy.

TL;DR: In this article, a review of the development of chemodynamic therapy (CDT) and its application in cancer treatment is presented, which summarizes the recent progresses of nanocatalyst-mediated CDT for antitumor application.
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Cell membrane coated-nanoparticles for cancer immunotherapy

TL;DR: In this article , the authors summarized the latest researches of biomimetic cell membrane-coated nanoparticles (CMCNs) for cancer immunotherapy, outline the existing specific cancer immune therapies, explore the unique functions and molecular mechanisms of various CMCNs, and analyze the challenges which CMCN faces in clinical translation.
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Nanovaccines with cell-derived components for cancer immunotherapy.

TL;DR: In this paper , the authors introduce the recent research progresses of those cell-derived biomimetic nanovaccines for cancer immunotherapy, and discuss the perspectives and challenges associated with the future clinical translation of these emerging vaccine platforms.
Journal ArticleDOI

Recent progress on nanomedicine-induced ferroptosis for cancer therapy.

TL;DR: In this article, the feasibility and properties of nanomedicine-based ferroptosis in cancer therapy is highlighted. And the current research on the applications of nanomedical applications for the ferroptic-based anticancer therapy are highlighted.
Journal ArticleDOI

Macrophage Cell Membrane‐Cloaked Nanoplatforms for Biomedical Applications

TL;DR: The present review covers the preparation and biomedical applications of macrophage cell membrane‐coated nanosystems, designed to combine the advantages of both macrophages and nanomaterials, improving the ability of those nanos systems to reach target sites.
References
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Journal ArticleDOI

The blockade of immune checkpoints in cancer immunotherapy

TL;DR: Preliminary clinical findings with blockers of additional immune-checkpoint proteins, such as programmed cell death protein 1 (PD1), indicate broad and diverse opportunities to enhance antitumour immunity with the potential to produce durable clinical responses.
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Stimuli-responsive nanocarriers for drug delivery

TL;DR: Recent advances in the design of nanoscale stimuli-responsive systems that are able to control drug biodistribution in response to specific stimuli, either exogenous (variations in temperature, magnetic field, ultrasound intensity, light or electric pulses) or endogenous (changes in pH, enzyme concentration or redox gradients).
Journal ArticleDOI

Oncology Meets Immunology: The Cancer-Immunity Cycle

TL;DR: Emerging clinical data suggest that cancer immunotherapy is likely to become a key part of the clinical management of cancer and may be more effective in combination with agents that target other steps of the cycle.
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