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DOI 10.3389/fimmu.2025.1530736

Медицинская библиотека · Frontiers in immunology · 2025

Intradermal delivery of SARS-CoV-2 RBD3-Fc mRNA vaccines via a needle-free injection system induces robust immune responses in rats.

Wang Cenrong, Tang Xin, Jiang Chenghan, Zhang Yu, Han Bo, Sun Yi, Guo Jianfeng, Peng Hanyu, Wang Zihan, Wang Yipeng, Zhang Jialu, Zhang Yong, Jiang Chunlai

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Аннотация

INTRODUCTION

Needle-free injection system (NFIS) is easy to operate and can decrease needle phobia. Besides, NFIS can increase the interaction of antigens in a more dispersed manner with immune cell at local injection site, which may improve the immune responses of mRNA vaccines. Although SARS-CoV-2 mRNA vaccines have great success, universal vaccines are urgently needed. Delivering universal mRNA vaccines by NFIS is preferred to combat COVID-19.

METHODS

RBD3-Fc mRNA expressing BA.4, Delta, and prototype RBD, and human IgG Fc with YTE mutation was designed and synthesized. The safety and immune responses of universal RBD3-Fc naked mRNA and mRNA-LNP vaccines delivered intradermally using NFIS (named GV-01) and intramuscularly via needles were evaluated and compared in rats.

RESULTS

The prime-boost regimen administered by two routes resulted in potent immune responses and intradermal delivery displays comparable or better performance in terms of binding antibodies, neutralizing antibodies and T cell responses. Naked mRNA vaccines were functional, but less effective than mRNA-LNP vaccines.

DISCUSSION: The above results suggest that RBD3-Fc vaccines are safe and immunogenic and NFIS can be used as an alternative to needles/syringes for the inoculation of mRNA-LNP vaccines to elicit robust systematic immune responses.

Для цитирования: Wang Cenrong, Tang Xin, Jiang Chenghan, Zhang Yu, Han Bo, Sun Yi, Guo Jianfeng, Peng Hanyu, Wang Zihan, Wang Yipeng, Zhang Jialu, Zhang Yong, Jiang Chunlai. Intradermal delivery of SARS-CoV-2 RBD3-Fc mRNA vaccines via a needle-free injection system induces robust immune responses in rats.. Frontiers in immunology. 2025. DOI: 10.3389/fimmu.2025.1530736.

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