4.8 Article

Mannose-Derived Carbon Dots Amplify Microwave Ablation-Induced Antitumor Immune Responses by Capturing and Transferring Danger Signals to Dendritic Cells

期刊

ACS NANO
卷 15, 期 2, 页码 2920-2932

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c09120

关键词

hepatocellular carcinoma; mannose-derived carbon dots; dendritic cells; immune responses; microwave ablation

资金

  1. National Natural Science Foundation of China (NSFC) [81971625, 81627803, 91859201, 81871374, 31630027, 32030060, 31971312]
  2. Chinese Postdoctoral Science Foundation [2019M653203]
  3. National Scientific Foundation Committee of Beijing
  4. Fostering Funds for National Distinguished Young Scholar Science Fund [JQ18021, 2018JQPY-002]
  5. National Clinical Research Center for Geriatric Diseases of Chinese PLA General Hospital [NCRCG-PLAGH-2019011]
  6. NSFC [31761133013, 51861135103]
  7. Ten Thousand Elite Plan [Y9E21Z11]
  8. CAS International Collaboration Project [E0632911ZX]

向作者/读者索取更多资源

Man-CD nanoparticles effectively capture danger signals after MWA and deliver them to dendritic cells, enhancing tumor-specific immune response and suppressing both primary and distant tumors. These nanoparticles serve as effective adjuvants to improve MWA therapy.
Hepatocellular carcinoma recurrence and metastasis after microwave ablation (MWA) are challenges in the clinic. This study showed that mannose-derived carbon dots (Man-CDs) could effectively capture several danger signals (DS) after MWA treatment and then deliver DS specifically to dendritic cells (DCs). This improved delivery of DS to DCs enhanced the processing and presentation of tumor-associated antigens by DCs. The results demonstrated that intratumoral injection of Man-CDs after MWA therapy elicited a potent tumor-specific immune response and finally led to the effective suppression of both primary and distant tumors. MWA + Man-CD treatment could efficiently reject tumor cell rechallenge in vivo. This study demonstrated that Man-CD nanoparticles are effective adjuvants that can improve MWA therapy by eliciting a tumor-specific immune response.

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