Amelioration of systemic antitumor immune responses in cocktail therapy by immunomodulatory nanozymes

Author:

Wang Shuren1ORCID,Wang Zhiyi1ORCID,Li Ziyuan23ORCID,Zhang Xiaoguang1,Zhang Hongtao4,Zhang Teng1,Meng Xiangxi5ORCID,Sheng Fugeng4,Hou Yanglong1ORCID

Affiliation:

1. Beijing Key Laboratory of Magnetoelectric Materials and Devices, School of Materials Science and Engineering, Beijing Innovation Centre for Engineering Science and Advanced Technology, Peking University, Beijing 100871, China.

2. Institute of Medical Technology, Peking University Health Science Center, Peking University, Beijing 100191, China.

3. Department of Biomedical Engineering, Peking University, Beijing 100871, China.

4. Department of Radiology, Fifth Medical Center of Chinese PLA General Hospital, Beijing 100071, China.

5. Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Key Laboratory for Research and Evaluation of Radiopharmaceuticals (National Medical Products Administration), Department of Nuclear Medicine, Peking University Cancer Hospital and Institute, Beijing 100142, China.

Abstract

Nanozymes that mimic natural enzyme–like activities have gradually emerged in cancer therapy. To overcome the bottlenecks of single-mode nanozymes, including “off-target” toxicity and ineffectiveness toward metastatic cancers, we designed magnetic nanoparticle–based multifunctional visualized immunomodulatory nanozymes. Besides the partial initiation of the prime immune response by intrinsic immunogenicity, as a smart drug delivery system with a temperature- and pH-sensitive dual response to the tumor microenvironment, these nanozymes released immune agonists to boost enhanced systemic immune response, eventually ameliorating the cancer immune microenvironment through many aspects: activating dendritic cells, improving the function of CD8 + T cells, and decreasing the population of myeloid-derived suppressor cells, which inhibited both primary and metastatic cancers. Mechanistically, these nanozymes regulated the reactive oxygen species–related Akt signaling pathway and consequently activated cell apoptosis–related signaling pathways, which provided a deeper understanding of the synergistic mechanism of multifunctional nanozymes. Our findings offer a promising imaging-guided cocktail therapy strategy through immunomodulatory nanozymes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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