Intranasal G5‐BGG/pDNA Vaccine Elicits Protective Systemic and Mucosal Immunity against SARS‐CoV‐2 by Transfecting Mucosal Dendritic Cells

• Published in: Advanced healthcare materials 2024-03, Vol.13 (6), p.e2303261-n/a
• Main Authors: Zhang, Han, Liu, Zezhong, Lihe, Hongye, Lu, Linwei, Zhang, Zongxu, Yang, Shengmin, Meng, Nana, Xiong, Yin, Fan, Xingyan, Chen, Zhikai, Lu, Weiyue, Xie, Cao, Liu, Min
• Format: Article
• Language: English
• Subjects: Antigens; Coronaviruses; COVID-19; Dendritic cells; Deoxyribonucleic acid; DNA; DNA delivery; G5‐BGG; IgG antibody; Immune system; Immunity; Immunoglobulin A; Immunoglobulin G; Infectious diseases; Lymphocytes; Lymphocytes T; Lymphoid tissue; Mucosal immunity; mucosal vaccine; Pandemics; Permeability; Plasmids; Robustness; Severe acute respiratory syndrome coronavirus 2; Vaccines; Viral diseases
• ISSN: 2192-2640; 2192-2659; 2192-2659
• DOI: 10.1002/adhm.202303261

Infectious disease pandemics, including the coronavirus disease 2019 pandemic, have heightened the demand for vaccines. Although parenteral vaccines induce robust systemic immunity, their effectiveness in respiratory mucosae is limited. Considering the crucial role of nasal‐associated lymphoid tissue (NALT) in mucosal immune responses, in this study, the intranasal complex composed of G5‐BGG and antigen‐expressing plasmid DNA (pSP), named G5‐BGG/pSP complex, is developed to activate NALT and to promote both systemic and mucosal immune defense. G5‐BGG/pSP could traverse mucosal barriers and deliver DNA to the target cells because of its superior nasal retention and permeability characteristics. The intranasal G5‐BGG/pSP complex elicits robust antigen‐specific immune responses, such as the notable production of IgG antibody against several virus variants. More importantly, it induces elevated levels of antigen‐specific IgA antibody and a significant expansion of the lung‐resident T lymphocyte population. Notably, the intranasal G5‐BGG/pSP complex results in antigen expression and maturation of dendritic cells in nasal mucosae. These findings exhibit the potential of G5‐BGG, a novel cationic material, as an effective gene carrier for intranasal vaccines to obtain robust systemic and mucosal immunity. The aim of this study is to develop a novel mucosal SARS‐CoV‐2 vaccine. It applies a novel nonviral vector, G5‐BGG, as an intranasal DNA vaccine vector. The plasmid coding SARS‐CoV‐2 spike protein is encapsulated by G5‐BGG. The formed gene complex is intranasally administrated into mice according to the given immune regime. Finally, humoral, mucosal, and cellular immunity are evaluated.