2019
DOI: 10.1021/acs.nanolett.9b00579
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Iron Nanoparticles for Low-Power Local Magnetic Hyperthermia in Combination with Immune Checkpoint Blockade for Systemic Antitumor Therapy

Abstract: Magnetic hyperthermia (MHT) utilizing heat generated by magnetic nanoparticles under alternating magnetic field (AMF) is an effective local tumor ablation method but can hardly treat metastatic tumors. In this work, we discover that pure iron nanoparticles (FeNPs) with high magnetic saturation intensity after being modified by biocompatible polymers are stable in aqueous solution and could be employed as a supereffective MHT agent to generate sufficient heating under a low-power AFM. Effective MHT ablation of … Show more

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Cited by 190 publications
(156 citation statements)
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“…However, almost 90% of cancer‐related death is due to metastasis rather than primary tumor growth . In recent years, cancer immunotherapy by stimulating the inherent immunological systems of the patients has shown tremendous prospect for inhibiting metastasized cancer . It is now established that radio‐, photo‐, and chemotherapy could cause cancer cell death in the primary lesion and induce dying tumor cells to release tumor‐associated antigens (TAAs) .…”
Section: Methodsmentioning
confidence: 99%
“…However, almost 90% of cancer‐related death is due to metastasis rather than primary tumor growth . In recent years, cancer immunotherapy by stimulating the inherent immunological systems of the patients has shown tremendous prospect for inhibiting metastasized cancer . It is now established that radio‐, photo‐, and chemotherapy could cause cancer cell death in the primary lesion and induce dying tumor cells to release tumor‐associated antigens (TAAs) .…”
Section: Methodsmentioning
confidence: 99%
“…Flow-Cytometry Analysis of T Lymphocytes and Macrophages in Primary Tumor and Spleen After 33 days, single-tumor and spleen cell suspensions were collected according to previously reported methods. [71][72][73] These cell suspensions were then cultured with anti-CD16/32 (catalog #101320) to block nonspecific binding to FcRs. Thereafter, various fluorochrome-conjugated antibodies such as CD3 (#100204), CD4 (#100559), CD8 (#100722), CD11c (#117343), MHC-II (#107626), F4/80 (#123146), and CD206 (#141721) were added to stain these cells according to the vendors' protocols.…”
Section: Articlementioning
confidence: 99%
“…Preclinical studies have demonstrated significant variations in how specific responses are elicited or augmented with heat. For instance, higher temperatures applied over a brief period may be best to augment CPI therapy [25] while trafficking of T cells to tumor may benefit from mild hyperthermia applied over a longer period of time [11]. Therefore, temperature gradients across a heated tumor may be helpful in eliciting wide ranging immunotherapeutic responses due to different dose profiles being associated with differing immune effects.…”
Section: Questions To Be Addressedmentioning
confidence: 99%