KERS‐Inspired Nanostructured Mineral Coatings Boost IFN‐γ mRNA Therapeutic Index for Antitumor Immunotherapy

Author:

Shao Zhenxuan1ORCID,Chen Liang1,Zhang Zengjie1,Wu Yan1,Mou Haochen1,Jin Xiaoqiang1,Teng Wangsiyuan1,Wang Fangqian1,Yang Yinxian2,Zhou Hao1,Xue Yucheng1,Eloy Yinwang1,Yao Minjun1,Zhao Shenzhi1,Cui Wenguo3ORCID,Yu Xiaohua1ORCID,Ye Zhaoming1ORCID

Affiliation:

1. Department of Orthopedic Surgery The Second Affiliated Hospital Zhejiang University School of Medicine Orthopedics Research Institute of Zhejiang University Key Laboratory of Motor System Disease Research and Precision Therapy of Zhejiang Province Clinical Research Center of Motor System Disease of Zhejiang Province 88 Jiefang Road Hangzhou City Zhejiang Province 310003 P. R. China

2. College of Pharmaceutical Sciences Zhejiang University Hangzhou 310058 China

3. Department of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics, Ruijin Hospital Shanghai Jiao Tong University School of Medicine 197 Ruijin 2nd Road Shanghai 200025 P. R. China

Abstract

AbstractTumor‐associated macrophage (TAM) reprogramming is a promising therapeutic approach for cancer immunotherapy; however, its efficacy remains modest due to the low bioactivity of the recombinant cytokines used for TAM reprogramming. mRNA therapeutics are capable of generating fully functional proteins for various therapeutic purposes but accused for its poor sustainability. Inspired by kinetic energy recovery systems (KERS) in hybrid vehicles, a cytokine efficacy recovery system (CERS) is designed to substantially augment the therapeutic index of mRNA‐based tumor immunotherapy via a “capture and stabilize” mechanism exerted by a nanostructured mineral coating carrying therapeutic cytokine mRNA. CERS remarkably recycles nearly 40% expressed cytokines by capturing them onto the mineral coating to extend its therapeutic timeframe, further polarizing the macrophages to strengthen their tumoricidal activity and activate adaptive immunity against tumors. Notably, interferon‐γ (IFN‐γ) produced by CERS exhibits ≈42‐fold higher biological activity than recombinant IFN‐γ, remarkably decreasing the required IFN‐γ dosage for TAM reprogramming. In tumor‐bearing mice, IFN‐γ cmRNA@CERS effectively polarizes TAMs to inhibit osteosarcoma progression. When combined with the PD‐L1 monoclonal antibody, IFN‐γ cmRNA@CERS significantly boosts antitumor immune responses, and substantially prevents malignant lung metastases. Thus, CERS‐mediated mRNA delivery represents a promising strategy to boost antitumor immunity for tumor treatment.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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