| Literature DB >> 34016473 |
Rika Nakahashi-Ouchida1, Yohei Uchida2, Yoshikazu Yuki3, Yuko Katakai4, Tomoyuki Yamanoue2, Hiromi Ogawa4, Yoshiko Munesue4, Nozomi Nakano4, Kouji Hanari4, Takashi Miyazaki5, Yuki Saito5, Shingo Umemoto6, Shin-Ichi Sawada7, Reshmi Mukerji8, David E Briles8, Yasuhiro Yasutomi9, Kazunari Akiyoshi7, Hiroshi Kiyono10.
Abstract
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.Entities:
Keywords: Cationic nanogel; Nasal vaccine; Non-human primate; Pneumonia; PspA
Year: 2021 PMID: 34016473 DOI: 10.1016/j.vaccine.2021.04.069
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641