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]
日期:2024-06-17
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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