Lipid Nanoparticle with 1,2-Di-O-octadecenyl-3-trimethylammonium-propane as a Component Lipid Confers Potent Responses of Th1 Cells and Antibody against Vaccine Antigen

抗体 抗原 脂质A 化学 纳米颗粒 固体脂质纳米粒 生物化学 病毒学 免疫学 生物 材料科学 纳米技术 脂多糖
作者
Atsushi Kawai,Masahiro Noda,Haruki Hirata,Lisa Munakata,Teppei Matsuda,Daiki Omata,Naoki Takemura,Sakura Onoe,Mika Hirose,Takayuki Kato,Tatsuya Saitoh,Toshiro Hirai,Ryo Suzuki,Yasuo Yoshioka
出处
期刊:ACS Nano [American Chemical Society]
卷期号:18 (26): 16589-16609
标识
DOI:10.1021/acsnano.4c00278
摘要

Adjuvants are effective tools to enhance vaccine efficacy and control the type of immune responses such as antibody and T helper 1 (Th1)- or Th2-type responses. Several studies suggest that interferon (IFN)-γ-producing Th1 cells play a significant role against infections caused by intracellular bacteria and viruses; however, only a few adjuvants can induce a strong Th1-type immune response. Recently, several studies have shown that lipid nanoparticles (LNPs) can be used as vaccine adjuvants and that each LNP has a different adjuvant activity. In this study, we screened LNPs to develop an adjuvant that can induce Th1 cells and antibodies using a conventional influenza split vaccine (SV) as an antigen in mice. We observed that LNP with 1,2-di-O-octadecenyl-3-trimethylammonium-propane (DOTMA) as a component lipid (DOTMA-LNP) elicited robust SV-specific IgG1 and IgG2 responses compared with SV alone in mice and was as efficient as SV adjuvanted with other adjuvants in mice. Furthermore, DOTMA-LNPs induced robust IFN-γ-producing Th1 cells without inflammatory responses compared to those of other adjuvants, which conferred strong cross-protection in mice. We also demonstrated the high versatility of DOTMA-LNP as a Th1 cell-inducing vaccine adjuvant using vaccine antigens derived from severe acute respiratory syndrome coronavirus 2 and
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