4.8 Article

Corn-like Au/Ag nanorod-mediated NIR-II photothermal/photodynamic therapy potentiates immune checkpoint antibody efficacy by reprogramming the cold tumor microenvironment

期刊

BIOMATERIALS
卷 268, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2020.120582

关键词

Corn-like Au/Ag nanorods; NIR-II PTT/PDT; Immunogenic cell death; Turning cold tumor microenvironment; Checkpoint blockade therapy

资金

  1. National Key R&D Program of China [2017YFA0205601]
  2. National Natural Science Foundation of China [51822302, 51773067, 31800831, 32071380, 51873222]
  3. Program for Guangdong Introducing Innovative and Entrepreneurial Teams [2017ZT07S054]
  4. Natural Science Foundation for Distinguished Young Scholars of Guangdong Province [2017B030306002]
  5. High-level Hospital Construction Project [DFJH201905]
  6. Science and Technology Program of Guangzhou [201804020060]
  7. Outstanding Scholar Program of Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory) [2018GZR110102001]
  8. Fundamental Research Funds for the Central Universities

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The study demonstrates that the corn-like Au/Ag nanorods, when combined with specific wavelength light irradiation, can induce immunogenic cell death of tumor cells, enhance T cell infiltration into tumors, and reprogram the immunosuppressive cold tumor microenvironment. Moreover, this combined treatment synergizes with immune checkpoint blocking antibodies to efficiently inhibit distant tumor growth and elicit a strong immunological memory effect against tumor recurrence.
Immune checkpoint blocking (ICB) antibodies have shown great success in the clinic, but their low response rate in patients with immunosuppressive cold tumors remains a huge challenge. Inspired by the capability of immunogenic cell death (ICD) to convert tumors from cold to hot, we developed a corn-like Au/Ag nanorod (NR) that can induce the ICD of tumor cells under 1064-nm light irradiation. The corn-like Au/Ag NRs plus NIR-II light irradiation strikingly increased the tumor infiltration of T cells and provoked a systemic immune response to reprogram the immunosuppressive cold tumor microenvironment; these NRs synergized with ICB antibodies to efficiently inhibit distant tumor growth. Encouragingly, the combination of aCTLA4 and Au/Ag NRs plus 1064nm light irradiation elicited a strong immunological memory effect that protected against tumor recurrence.

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