免疫原性
纳米凝胶
佐剂
肺炎链球菌
微生物学
鼻腔给药
肺炎球菌感染
接种疫苗
免疫学
免疫系统
生物
化学
药物输送
有机化学
抗生素
作者
Rika Nakahashi-Ouchida,Yohei Uchida,Yoshikazu Yuki,Yuko Katakai,Tomoyuki Yamanoue,Hiromi Ogawa,Yoshiko Munesue,Nozomi Nakano,Kouji Hanari,Takashi Miyazaki,Yuki Saito,Shingo Umemoto,Shin‐ichi Sawada,Reshmi Mukerji,David E. Briles,Yasuhiro Yasutomi,Kazunari Akiyoshi,Hiroshi Kiyono
出处
期刊:Vaccine
[Elsevier]
日期:2021-05-17
卷期号:39 (25): 3353-3364
被引量:44
标识
DOI:10.1016/j.vaccine.2021.04.069
摘要
Current polysaccharide-based pneumococcal vaccines are effective but not compatible with all serotypes of Streptococcus pneumoniae. We previously developed an adjuvant-free cationic nanogel nasal vaccine containing pneumococcal surface protein A (PspA), which is expressed on the surfaces of all pneumococcal serotypes. Here, to address the sequence diversity of PspA proteins, we formulated a cationic nanogel-based trivalent pneumococcal nasal vaccine and demonstrated the vaccine's immunogenicity and protective efficacy in macaques by using a newly developed nasal spray device applicable to humans. Nasal vaccination of macaques with cationic cholesteryl pullulan nanogel (cCHP)-trivalent PspA vaccine effectively induced PspA-specific IgGs that bound to pneumococcal surfaces and triggered complement C3 deposition. The immunized macaques were protected from pneumococcal intratracheal challenge through both inhibition of lung inflammation and a dramatic reduction in the numbers of bacteria in the lungs. These results demonstrated that the cCHP-trivalent PspA vaccine is an effective candidate vaccine against pneumococcal infections.
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