4.8 Article

Graphdiyne oxide nanosheets reprogram immunosuppressive macrophage for cancer immunotherapy

Journal

NANO TODAY
Volume 45, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.nantod.2022.101543

Keywords

Graphdiyneoxide; Macrophagepolarization; Tcell; Cancerimmunotherapy

Funding

  1. National Basic Research Program of China [2021YFA1200900, 2020YFA0710700]
  2. Program for International S&T Cooperation Projects of the Ministry of Science and Technology of China [2021YFE0112600, 2018YFE0117200]
  3. Chinese Academy of Medical Sciences (CAMS) Innovation Fund for Medical Science [CIFMS 2019-I2M-5-018]
  4. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB36000000]
  5. Research and Development Project in Key Areas of Guangdong Province [2019B090917011]
  6. National Natural Science Foundation of China [32071402, 22027810, 11621505, 22071251, 21875258]
  7. NSFC Major Research Plan-Integrated Program [92143301]
  8. China Postdoctoral Science Foundation [2021TQ0085]

Ask authors/readers for more resources

Graphdiyne oxide (GDYO) nanosheets exhibit excellent properties and have the potential to be used in biomedical applications. In this study, it was found that M2-like macrophages could kill cancer cells with GDYO treatment by activating pro-inflammatory pathways. Intraperitoneal injection of GDYO also reduced tumor growth in a melanoma-bearing mouse model. Additionally, GDYO activated cytotoxic T cells directly or indirectly through macrophages, enhancing the response to checkpoint inhibitors in a breast cancer model. GDYO has the potential to enhance the efficacy of cancer immunotherapy by activating both the innate and adaptive arms of the immune system.
Graphdiyne oxide (GDYO) nanosheets have remarkable electronic, mechanical, and thermal properties, which is hoped to act a better alternative for biomedical applications. Tumor-associated macrophage (TAM) is a promising cell population for nanotechnology application to cancer immunotherapy. In the present study, we found M2-like macrophages can be polarized to kill cancer cells with GDYO treatment via acti-vation of pro-inflammatory pathways and GDYO injected intraperitoneally reduced tumor growth in a melanoma-bearing mouse model. In addition, GDYO activated cytotoxic T cells either directly or indirectly via macrophages, enhancing checkpoint inhibitor response in a breast cancer model. We expect that GDYO has invoked both the innate and adaptive arms of the immune system that are likely to enhance efficacy of cancer immunotherapy. (c) 2022 Elsevier Ltd. All rights reserved.

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