4.8 Article

NIR-II Responsive Molybdenum Dioxide Nanosystem Manipulating Cellular Immunogenicity for Enhanced Tumor Photoimmunotherapy

期刊

NANO LETTERS
卷 22, 期 12, 页码 4741-4749

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.2c00899

关键词

second near-infrared photothermal therapy; molybdenum dioxide; immunogenic cell death; caspase 8; tumor immunotherapy

资金

  1. National Natural Science Foundation of China [11874021, 62175071, 32071399]
  2. Science and Technology Program of Guangzhou [2019050001, 201904010323]
  3. Guangdong Basic and Applied Basic Research Foundation [2021A1515011988, 2021A1515110265]
  4. Shenzhen Science and Technology Program [RCBS20210706092347040]
  5. Research Start-up Fund of Postdoctoral of SAHSYSU [ZSQYRSFPD0031]
  6. Open Foundation of Key Laboratory of Optoelectronic Science and Technology for Medicine (Fujian Normal University), Ministry of Education, China [JYG2009]

向作者/读者索取更多资源

A new nanosystem for tumor photoimmunotherapy in the second near-infrared window has been developed. This system uses molybdenum dioxide nanodumbbells as nanoconverters and incorporates an apoptosis-blocking strategy to improve immunogenic cell death. The system effectively activates systemic immunity to inhibit tumor growth and metastasis and enhances responses to immune checkpoint inhibitors.
Photothermal therapy (PTT) in the second near-infrared (NIR-II) window has emerged as a better candidate for deep-tissue tumor elimination. More interestingly, the photothermal ablated tumor cells also manifest somewhat immunostimulation potency to elicit antitumor immunity, although most dying cells are undergoing apoptosis that is commonly considered as immunologically silent. Here, a NIR-II responsive nanosystem is established for tumor photoimmunotherapy using molybdenum dioxide (MoO2) nanodumbbells as the nanoconverter. Meanwhile, an apoptosis-blocking strategy is proposed to regulate the cell death pattern under NIR-II laser irradiation in order to improve the immunogenic cell death. The nanoformulation can efficiently block caspase 8-dependent apoptotic pathway in photothermal ablated tumor cells and transform into more immunogenic death patterns, thereby activating systemic immunity to inhibit tumor growth and metastasis. In addition, this strategy also helps enhance the body's responses to alpha-PD-1 immune checkpoint inhibitor, which implies a potential optimal combination for cancer immunotherapy.

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